Curriculum vitae | Codrina Irena Mihaela ANCUTA mar 2015 Facultate de Medicina... · 1 | P a g e...

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Curriculum vitae | Codrina Irena Mihaela ANCUTA 1 | Page CURRICULUM VITAE Nume si prenume: ANCUTA Codrina Irena Mihaela Nume anterior casatoriei: CHIRIEAC Locul si data nasterii: Adresa:; Date contact: Stare civila: Pozitie profesionala si academica actuala medic primar specialitatea Reumatologie; medic primar specialitatea Recuperare Medicala, Medicina Fizica si Balneologie; doctor in medicina; sef lucrari univ Disciplina Reumatologie-Balneofizioterapie, Departamentul Medicale II, Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi; coordonator Centru EUSTAR 162 Loc de munca actual 1 Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi, Facultatea de Medicina, Disciplina Reumatologie – Balneofizioterapie (din 1995); 2 Spitalul Clinic de Recuperare Iasi, Clinica Reumatologie II, sef clinica (din 2013); Studii 1984-1988: Liceul “Emil Racovita”, profil matematica-fizica; absolventa a promotiei iunie 1998, diploma de bacalaureat seria E Nr.39358 (media generala examen bacaureat 9.62); 1988-1994: Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi, Facultatea de Medicina; absolventa a promotiei 1994, diploma de medic - doctor: diploma M nr. 041128; media generala de promovare a anilor de studiu 9.98; media generala de licenta 9.99 (sesiunea sept 1994); Titluri stiintifice Doctor in Medicina (seria E nr. 0002743) (ordin MEC nr 3824/03.05.2006); titlul tezei: Miopatia inflamatorie in poliartrita reumatoida/ Inflammatory myopathy in rheumatoid arthritis conducator de doctorat: prof univ dr George Ioan Pandele; 1998-2005: doctorand, data sustinerii tezei de doctorat: 15 iulie 2005 Experienta in specialitate si locuri de munca relevante 01.02.1995-02.10.1995: medic rezident specialitatea Pneumoftiziologie prin concurs (OMS 2213/1994), Spitalul Clinic de Pneumoftiziologie Iasi Reumatologie 1996-1999: medic rezident in specialitatea Reumatologie (OMS nr. 715/27.03.1996), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi 1999 -2003: medic specialist Reumatologie (OMS nr. 900/ 20.10.1999; medie 9.17), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi din 2003: medic primar specialitatea Reumatologie (OMS nr. 846/ 12.09.2003; medie 9.66), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi Recuperare Medicala, Medicina Fizica si Balneologie

Transcript of Curriculum vitae | Codrina Irena Mihaela ANCUTA mar 2015 Facultate de Medicina... · 1 | P a g e...

Curriculum vitae | Codrina Irena Mihaela ANCUTA

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CURRICULUM VITAE

Nume si prenume: ANCUTA Codrina Irena Mihaela

Nume anterior casatoriei: CHIRIEAC

Locul si data nasterii:

Adresa:;

Date contact:

Stare civila:

Pozitie profesionala si academica actuala

medic primar specialitatea Reumatologie; medic primar specialitatea Recuperare Medicala, Medicina Fizica si Balneologie; doctor in medicina; sef lucrari univ Disciplina Reumatologie-Balneofizioterapie, Departamentul Medicale II,

Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi; coordonator Centru EUSTAR 162

Loc de munca actual

1Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi, Facultatea de Medicina, Disciplina Reumatologie – Balneofizioterapie (din 1995);

2Spitalul Clinic de Recuperare Iasi, Clinica Reumatologie II, sef clinica (din 2013);

Studii

1984-1988: Liceul “Emil Racovita”, profil matematica-fizica; absolventa a promotiei iunie 1998, diploma de bacalaureat seria E Nr.39358 (media generala examen bacaureat 9.62);

1988-1994: Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi, Facultatea de Medicina; absolventa a promotiei 1994, diploma de medic - doctor: diploma M nr. 041128; media generala de promovare a anilor de studiu 9.98; media generala de licenta 9.99 (sesiunea sept 1994);

Titluri stiintifice

Doctor in Medicina (seria E nr. 0002743) (ordin MEC nr 3824/03.05.2006); titlul tezei: Miopatia inflamatorie in poliartrita reumatoida/ Inflammatory myopathy in

rheumatoid arthritis conducator de doctorat: prof univ dr George Ioan Pandele; 1998-2005: doctorand, data sustinerii tezei de doctorat: 15 iulie 2005

Experienta in specialitate si locuri de munca relevante

01.02.1995-02.10.1995: medic rezident specialitatea Pneumoftiziologie prin concurs (OMS 2213/1994), Spitalul Clinic de Pneumoftiziologie Iasi

Reumatologie

1996-1999: medic rezident in specialitatea Reumatologie (OMS nr. 715/27.03.1996), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi

1999 -2003: medic specialist Reumatologie (OMS nr. 900/ 20.10.1999; medie 9.17), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi

din 2003: medic primar specialitatea Reumatologie (OMS nr. 846/ 12.09.2003; medie 9.66), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi

Recuperare Medicala, Medicina Fizica si Balneologie

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1999-2002: medic rezident in specialitatea Recuperare, Medicina Fizica si Balneologie, Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi

2002-2008: medic specialist Recuperare, Medicina Fizica si Balneologie (OMS nr 256/11.04.2002; media 9.33), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi

din 2008: medic primar specialitatea Recuperare, Medicina Fizica si Balneologie (OMS 1971/03.12.2008; media 10.00), Clinica de Reumatologie, Spitalul Clinic de Recuperare Iasi

Experienta didactica si locuri de munca relevante

2.10.1995-01.03.1999: preparator universitar prin concurs, Disciplina Reumatologie-Balneofizioterapie, Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi

05.03.1999-01.03.2004: asistent universitar prin concurs (decizia 2825/05.03.1999), Disciplina Reumatologie-Balneofizioterapie, Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi

din 01.03.2004 - in prezent: Sef lucrari univ prin concurs, Disciplina Reumatologie-Balneofizioterapie, Universitatea de Medicina si Farmacie “Gr.T.Popa” Iasi

Cursuri de formare medicala (nationale, internationale) si specializari

Nationale

Curs Management Spitalicesc, Scoala Nationala de Sanatate Publica si Management Sanitar, 14.02-28.03.2008, Bucuresti, Romania (seria A, nr. 00331);

Supraspecializare in Boli osoase endocrino-metabolice (certificate de absolvire curs seria D, Nr 0011216) martie-nov 2003, Iasi, Romania; Certificat de supraspecializare in Patologie osoasa endocrino-metabolica seria C Nr. 013718

Curs Laser-terapie, 01.03-31.05.2001, Iasi, Romania, certificate de absolvire curs seria A, nr 0009588

Curs intensiv Metode moderne de tratament al copilului spastic, 21-23.09.2000, Bucureti, Romania

Curs postuniversitar Algeziologie (durerea si tratamentul ei), 23.04-21.05.1999, UMF “Gr,T.Popa” Iasi (certificat de absolvire seria B, nr 0003658)

Internationale

Curs imagistica: Imagistica in bolile reumatice, 01 oct 2014, Bucuresti, Romania 3rd Annual Meeting of the Lupus Academy, 7-9 March 2014 Berlin, Germany Pain Refresher Course, 2nd May 2013, Singapore 2nd SE Europe Course Systemic Lupus Erythematosus, 25.09.2013, Bucuresti, Romania APLAR Musculoskeletal Ultrasound Course in Rheumatology, The 15th Congress pf the Asia

Pacific League of Associatios for Rheumatology, 10-14 Sept 2012, Dead Sea, Amman, Jordan Al doilea Curs International de Ecografie Musculoscheletala sub patronaj stiintific EULAR, 8-10

martie 2012 Bucuresti, Romania Workshop: Methodentransfer und neue knozepte rheumatologie, 2-4 Jun 2011, Chisinau, Moldova. ISCD Clinician Bone Densitometry Course, 25-26 feb 2011, Bucharest, Romania. ISCD and IOF FRAX Initiative: Interpretation and Use of FRAX in Clinical Practice, 11-13 nov 2010,

Bucharest, Romania. Curs Internaţional de Osteoporoză cu Certificare în Osteodensitometrie, IOF-OsArt, 27-28 mai

2009, Sinaia, Romania. 6th RCRD International Workshop: Up-to-date in Rheumatology, 27-29 apr 2009, Bucharest,

Romania The 1st Quantitative Ultrasound Densitometry Course, 3-4 july 2008, Bucharest & Iasi Curs EUSTAR: Scleroderma Skin Scoring Course, 11 jul 2008, Cluj-Napoca, Romania Academy of Rheumatology, 18-20 dec 2008, Cairo, Egipt

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Program educational de armonizare a managementului PR precoce in concordanta cu recomandarile EULAR- Eupera, Sanofi Aventis (Universitatea Paris VII Franta; platforma electronica www.eupera.org)

Workshop New evidence-based pain control: oxycodone in severe somatic, neuropatic and visceral pain, 23-27 March 2007, Paris, France

4th RCRD (Research Centre on the pathology and treatment of Rheumatic Disorder) International Workshop: Outcomes in Rheumatology, 6-8 dec 2007, Bucharest, Romania (European Commission FP6)

Musculoskeletal ultrasound course, 19-21 Jan 2007, Bucharest, Romania Curs International de Osteoporoza cu Certificare in Osteodensitometrie, 11-14 apr 2007, Cluj-

Napoca, Romania 14th EULAR Intermediate Sonography Course, 10-13 June 2007, Sitges, Barcelona, Spania (sub

patronaj stiintific EULAR) (bursa studiu EULAR); 1st RCRD International Workshop: Advanced Techniques in Bone Research, 28-30 sep 2006

Bucuresti, Romania ISCD Bone densitometry Course, 29-30 sept 2006, Bucuresti, Romania International Musculo-skeletal Sonography Course (EULAR, OSART), 13-16 apr 2005, Cluj-Napoca,

Romania Advancing arthritis therapy: addressing patient needs, 4 Feb 2006, Seville Spain 9th EULAR Sonography Course (from introductory to advanced practical course on musculoskeletal

sonograhy), 9-12 Dec 2004, Paris, France (sub patronaj EULAR) (bursa de studiu EULAR); 1st European Course–Capillaroscopy and Rheumatic Diseases, 10-12 Sep 2004, Genova, Italy (bursa

EULAR); John Humphrey International Course of Immunology on self-tolerance and self-recognition, 15-19

May 2000, Sinaia, Romania; (sub patronaj European Federation of Immunological Societies, RSI, Romanian Society for Immunology – Iasi Branch)

6th EULAR Postgraduate Course in Rheumatology, 18-27 June 2000, Nice, Franta (sub patronaj EULAR) (bursa de studiu EULAR);

30 aug-03 sep 1992, John Humphrey Course on Tumor Immunology, Iasi, Romania

Cursuri Good Clinical Practice (GCP)

CME Program SCEPTER, Introduction to the Clinical Drug Development Process: ICH Good Clinical Practice for Clinical Trial Sites, web-training, 04 Jan 2012

Quintiles Global Learning & Development, Introduction to the Clinical Drug Development Process: ICH Good Clinical Practice for Clinical Trial Sites, web-training, 03 Jan 2012

Pfizer GCP for Investigational Site Staff, Pfizer Partner Learning Solution, web-training, 11 feb 2011

FLEX-LA294 Investigator Meeting, 28029 apr 2011, Barcelona, Spain

Membru al asociaţiilor si organizatiilor profesionale (nationale, europene)

Internationale: EUSTAR (EULAR Scleroderma Trials and Research); IASP (International Association for the Study of Pain) si SIG musculoskeletal pain (subgroup durere musculo-scheletala); ECTS (European Calcified Tissue Society); EMEUNET; Autoimmunity network

Nationale: Societatea Romana de Reumatologie; Asociatia de Recuperare Nord Est (membru fondator; 2009); RHEUMA-NORD EST – asociatie profesionala reumatologie (presedinte si membru fondator; 2014); Colegiul Medicilor din Romania (CMI 2409/05.10.2011)

Limbi de circulatie internationala cunoscute

Engleza – nivel B2 (atestat EuroEd, certificat absolvire nr 019/05 dec 2010; certificat de absolvire Funny English center Curs avizat de Ministerul Invatamintului nr 25410/18.03.1997 si Autorizat Consiliul National de Formare a Adultilor decizia 22/240 din 11.04.2008);

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Franceza (nivel B2; atestat DALF- Diplome Approfondi de la Langie Francais 12/04/1995 – no 04000100097)

Membru în colectivele de redacție ale revistelor de specialitate, in consiliul peer-review

Membru in Colegiul de Redactie al Revistei Romane de Reumatologie

Invited peer-reviewer pentru reviste cotate ISI (Clinical Rheumatology, European Journal of Physical and Rehabilitation Medicine);

Membru consiliul peer-review al Revistei Romane de Reumatologie (Editura Medicala Amaltea, Bucuresti; ISSN: 1843-0791; eISSN: 2069-6086, Cod CNCSIS: 378, B+)

Invited peer-reviewer pentru reviste BDI (Journal of Dentistry, Medicine and Medical Sciences);

Premii si distinctii

Premiu de Excelenta in Reumatologie, Societatea Romana de Reumatologie pentru lucrarea Model matematic de predicție a obținerii remisiunii SDAI în poliartrita reumatoidă, Trifan AE, Pomîrleanu C, Miu S, ANCUTA C, comunicare orala la CNR 2014 Bucuresti, Romania;

Diploma de merit, lucrarea Terapia cu Infliximab si sarcina – o provocare a etapei moderne, Cardei M, ANCUTA C, Ancuta E, Stoica S, Zugravu G, Chirieac R, Sesiunea comunicari orale Simpozionul Conect 2008 – Remicade la puterea a 6-a, 30 mai 2008, Bucuresti, Romania;

Mentiune lucrarea Infliximab, eficacitate si tolerabilitate in artropatia psoriazica, ANCUTA C et al, sesiunea postere, Simpozionul Conect 2008 – Remicade la puterea a 6-a, 30 mai 2008, Bucuresti, Romania;

Premiul de excelenta in medicina TNL, Gala Tinerilor valori editia IV, 24 feb 2009, Iasi, Romania

Recunoastere in Marquis Who's Who; Ancuta Codrina Mihaela Irena is recognized in Marquis

Who's Who. : physician, educator, Location: Iasi; Country: Romania;

http://bios.marquiswhoswho.com/ancuta_codrina_mihaela_irena/physician_educator/8309281

Activitate didactica, cercetare stiintifica si clinica/ de asistenta medicala (vezi Lista completa de lucrari anexata)

Activitatea profesionala desfasurata in cadrul UMF “Gr.T.Popa” Iasi si in Clinica Reumatologie, Spitalul Clinic de Recuperare Iasi (integrare cu ½ norma) s-a conturat pe trei directii principale, respectiv didactica, de cercetare stiintifica si activitatea clinica. O sinteza a acestor coordonate releva urmatoarele:

articole publicate in extenso in reviste cotate ISI: (30) (11 articole in calitate de autor principal; 19 articole coautor) (vezi lista completa lucrari anexata);

articole publicate in rezumat in reviste cotate ISI: (86) (42 autor principal, 44 coautor) (vezi lista completa lucrari anexata);

articole in extenso in reviste indexate in BDI: (85) (39 autor principal, 46 coautor) (vezi lista completa lucrari anexata);

articole in rezumat in reviste indexate in BDI sau volume manifestari stiintifice cu si fara ISBN: (76) (39 autor principal, 37 coautor) (vezi lista completa lucrari anexata);

carti, manuale, monografii: carte internationala (4 capitole); carte nationala (1 editor, 4 autor unic, 1 membru in colectiv de autori, 13 autor capitol); (vezi lista completa lucrari anexata)

participare la manifestari stiintifice internationale si nationale: (201 prezentari) (75 comunicari orale, 126 postere): international (4 autor principal si 20 coautor), national (25 autor principal si 26 coautor) (comunicari orale); international (44 autor principal si 37coautor) national ( 23 prim autor, 22 coautor) (postere); (vezi lista completa lucrari anexata)

lector la manifestari stiintifice: 110 manifestari nationale (vezi lista completa lucrari anexata)

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granturi/contracte de cercetare/ studii multicentrice: granturi internationale (14) (2 director de grant; 2 director partener national in consortiu international; 10 membru in colective internationale); granturi nationale (4) (membru in echipa grant); studii multicentrice postmarketing (14) (4 investigator principal in studii internationale; 10 investigator principal in studii nationale); studii multicentrice randomizate (53) (9 investigator principal; 44 – subinvestigator/coordonator de studiu)

citari in articole: (272) (254 ISI, 18 BDI)

Articolele/studiile in extenso in reviste din fluxul stiintific international principal si BDI, publicatiile in rezumat, participarile cu comunicari orale sau postere la manifestari stiintifica internationale si nationale, activitatea editoriala se regasesc punctate in lista completa de lucrari.

Granturi/contracte de cercetare/ studii multicentrice

Director grant international (2)

1. IASP Grant: Musculoskeletal pain academy, 2011, IASP Developing Countries Project: Initiative for improving pain education; jul2011-jul2012; (acord UMF “Gr.T.Popa” Iasi nr.12119/28.06.2011); finantare IASP 7000 USD; http://www.iasp-pain.org/Education/Content.aspx?ItemNumber=954;

http://www.musculoskeletal.pain-academy.com

Proiectul este focusat pe aspectele multivalente ale durerii musculo-scheletale, cu interpretare interdisciplinara, atat din perspectiva specialistului in reumatologie, cat si a particulatilor de definire a durerii in contextul sarcinii ce survine la o pacienta cu patologie reumatismala (prezentand punctul de vedere a obstetricianului), a patologiei musculo-scheletale ce se dezvolta la practicianul stomatolog.

2. EUSTAR Clinical Project CP34: Early Accelerated Atherosclerosis in Systemic Sclerosis (SSAS), grant EUSTAR 2011-2015; UCN-EUSTAR162 (nr.12428/30.06.2011) membri echipa cercetare: Carmen Marina Mihai, UMF Bucuresti (UCN-EUSTAR 100); Valeria Ricerri, Jose Luis Rosales-Alexander (UCN-EUSTAR 094), Patricia Carreira P (UCN-EUSTAR 023), Maria Joao Salvador (UCN-EUSTAR 068), Juan José Alegre Sancho (UCN EUSTAR 123); http://www.eustar.org/ClinicalTrial.html

Colaborarea multicentrica raportat la clarificarea profilului ATS accelerate in sclerodermia sistemica, cu explorare complexa (biomarkeri surogat biologici si imagistici), in dinamica doar pentru subgrupul de pacienti cu incadrare nationala, cu insertie de asemenea interdisciplinara; date preliminare prezentate in analiza subgroup UCN EUSTAR 162 la congrese internationale; lucrare prezentata la Congresul National de Reumatologie oct 2014, Bucuresti, Romania

ANCUTA C, Pomirleanu C, Belibou C, Grosu C, Mihai CM, Magda SL, Carreira P, Rosales-Alexander JL, Ricerri V, Salvador MJ, Chirieac R, Surrogate biomarkers for subclinical atherosclerosis in systemic sclerosis: an interim analysis of the SSAS cohort, Revista Romana de Reumatologie 2014, XXIII (supliment): 78;

Director partener national in consortiu international (2)

1. EULAR Orphan Disease Program Observational study of treatment outcome in early diffuse cutaneous systemic sclerosis; Chief Investigator Professor Ariane Herrick (University of Manchester); Funder EULAR Orphan Disease Program (Funding Reference Number R111788); Acord colaborare nr. 13517/14.07.2011 Universitatea Manchester-U.M.F. “Gr.T.Popa” Iasi (jul2011-ian2014); director proiect UMF Iasi: dr. ANCUTA Codrina; finantare EULAR ODP 312 EURO/patient; 17 pacienti inrolati (5300 Euro); http://www.ssc-esos.net/home.asp; http://www.eular.org/ (activitatea site UMF Gr.TPopa Iasi – al treilea ca si activitate de recrutare a pacientilor SSc in cadrul proiectului de cercetare)

2. International EU-funded Research Project (FP7): DEsschipher, to decipher the optimal management of systemic sclerosis, http://www.eustar.org/desscipher.html ; http://www.uni-

giessen.de/fbz/fb11/institute/klinik/rheumatologie/desscipher-en?set_language=en ; https://www.uni-

giessen.de/fbz/fb11/institute/klinik/rheumatologie/desscipher-en/about-desscipher/contributing-

centers/contributing-centers

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OT 1: Prevention and treatment of digital ulcers, Marco MATUCCI-CERINIC (UNIFI), Francesco

DELGADO (LEEDS), NCT01836263;

http://clinicaltrials.gov/ct2/show/NCT01836263?term=desscipher&rank=5

OT2: Improvement of hand dysfunction by arthritis, principal investigator László CZIRJÁK,

NCT01834157, http://clinicaltrials.gov/ct2/show/NCT01834157?term=desscipher&rank=2

OT3: Prevention and treatment of interstitial lung disease (lung fibrosis), principal investigator

Gabriela RIEMEKASTEN (CHARITÉ), Christopher DENTON (UCL), NCT01858259;

http://clinicaltrials.gov/ct2/show/NCT01858259?term=desscipher&rank=1

OT4: Development and prevention of pulmonary hypertension, principal investigators: Yannick

ALLANORE, Jérôme AVOUAC (UPD), NCT01840748;

http://clinicaltrials.gov/ct2/show/NCT01840748?term=desscipher&rank=4

OT5: Development and prevention of severe heart disease, PI: Gabriele VALENTINI (UNINA2),

NCT01829126, http://clinicaltrials.gov/ct2/show/NCT01829126?term=desscipher&rank=3

Proiect de cercetare castigat si finantat prin program European FP7, ambitios prin dezvoltarea multicentrica, pe 5 directii de studiu, vazand afectarea viscerala cu relevanta vitala si impact functional si asupra calitatii vietii, aflat in stadiul de recrutare a pacientilor pe teme de interes.

Membru in colectiv international (10)

1. IASP Grant IASP Developing Countries Project: Initiative For Improving Pain Education - Grant IASP (International Association for the Study of Pain); Manager de proiect dr. Jaba Irina 05.2009-05.2010; http://www.iasp-pain.org/Education/Content.aspx?ItemNumber=954 acord UMF Iasi 8499/20.05.2009; finantare IASP 9700 USD

Publicare ghid practic de terapie a durerii cronice – participare cu doua capitol - primul cu insertie cai patofiziologice, metode de cuantificare si terapie farmacologica a durerii cronice msculocheletale, cel de-al doilea cu raportare la terapia fizicala si de reabilitare

ANCUTA C. Durerea cronica musculo-scheletala. In: Mungiu OC, Jaba IM (ed) Managementul durerii –

ghid practic (grant IASP: Initiative for Improving Pain Education), Editura “Gr.T.Popa”, UMF Iasi 2010,

ISBN: 978-973-7682-98-7 (pg 113-142);

ANCUTA C, Managementul non-farmacologic al durerii cronice musculo-scheletale. In: Mungiu

OC, Jaba IM (ed) Managementul durerii – ghid practic (grant IASP: Initiative for Improving Pain

Education), Editura “Gr.T.Popa”, UMF Iasi 2010, ISBN: 978-973-7682-98-7 (pg 206-210);

2. PROTOCOL QUEST-RA 2009-2011: Quantitative Patient Questionnaire Monitoring in Standard Clinical Care of Patients with Rheumatoid Arthritis (QUEST-RA), Manager de proiect Tuulikki SOKKA (Finland), 2009-2011 (grant cu finantare internationala si locala Abbvie)

3. PROTOCOL QUEST-RA 2013-2014: Treating Rheumatoid Arthritis to Target: Are Recommendations met? A Multinational Study of Patients with Rheumatoid Arthritis who Receive Usual Care in 33 Countries; Manager de proiect Tuulikki SOKKA (Finland), 2013-2014 (aviz nr 6680/01.04.2013) (grant cu finantare internationala si locala Abbvie)

Protocol de studiu complex, cu incadrare multinationala (33 tari) si multicentrica, cu o cuantificare atat de moment (pacienti consecutivi) a normelor de practica cotidiana in poliartrita reumatoida cu specificitate nationala, dar si cu evaluare in dinamica (vizite predefinite in cadrul studiului), cu raportare la recomandarile T2T formulate de EULAR.

Pt protocoalele 2 si 3, rezultatele au fost diseminate in cadrul manifestari EULAR si ACR, dar si prin numeroase publicatii in fluxul international ISI. Intre acestea, participarea directa in:

Grøn et al, The association of fatigue, comorbidity burden, disease activity, disability and gross

domestic product in patients with rheumatoid arthritis. Results from 34 countries participating in

the Quest-RA program. Clinical and Experimental Rheumatology [2014] (PMID:25327997); Clin Exp

Rheumatol. 2014 Nov-Dec;32(6):869-77. Epub 2014 Oct 20 IF=2.973;

http://europepmc.org/abstract/med/25327997;; http://www.ncbi.nlm.nih.gov/pubmed/25327997

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Khan NA, ANCUTA C, Patient's global assessment of disease activity and patient's assessment of

general health for rheumatoid arthritis activity assessment: are they equivalent? Ann Rheum Dis.

2012 Dec;71(12):1942-9. doi: 10.1136/annrheumdis-2011-201142. Epub 2012 Apr 24. IF=9.11;

http://ard.bmj.com/content/71/12/1942.short

Khan NA, ANCUTA C, Determinants of discordance in patients' and physicians' rating of rheumatoid

arthritis disease activity. Arthritis Care Res (Hoboken). 2012 Feb;64(2):206-14. doi: 10.1002/acr.20685.

IF=4.039; http://onlinelibrary.wiley.com/doi/10.1002/acr.20685/full

Sokka T, QUEST-RA. Work disability remains a major problem in rheumatoid arthritis in the 2000s:

data from 32 countries in the QUEST-RA study. Arthritis Res Ther. 2010;12(2):R42. doi: 10.1186/ar2951.

Epub 2010 Mar 12.; IF=4.357; http://www.ncbi.nlm.nih.gov/pubmed/20226018

Participare in 6 protocoale in colaborare multinationala multicentrica EUSTAR in cadrul UCN EUSTAR 162, si anume:

4. EUSTAR Project CP18: Digital Ulcers secondary to Systemic sclerosis AC-052-513 - grant EUSTAR Research group and Actelion EUSTAR (Project leader: Prof. Ulrich Walker; Actelion Project leader: Monika Brand; Project manager: Dr Rebecca Hollaender) (Nov 2009 – Oct 2010); http://www.eustar.org/ClinicalTrial.html

5. EUSTAR Clinical Project: Very Early Diagnosis of Systemic Sclerosis VEDOSS, 2010-2015 (2020), , PROJECT manager: prof dr. Marco Matucci Cerinic ; aviz nr. ; http://www.eustar.org/Vedoss.html (6681/01/04.2013)

Minier et al (EUSTAR co-workers), Preliminary analysis of the Very Early Diagnosis of Systemic

Sclerosis (VEDOSS) EUSTAR multicentre study: evidence for puffy fingers as a pivotal sign for

suspicion of systemic sclerosis. Ann Rheum Dis. 2014 Dec;73(12):2087-93. doi: 10.1136/annrheumdis-

2013-203716. Epub 2013 Aug 12.; IF=9.270; http://www.ncbi.nlm.nih.gov/pubmed/23940211

6. EUSTAR Clinical Project: MEDS; http://www.eustar.org/MedsOnline.html (aviz nr 12528/10.07.2009)

Meier et al EUSTAR Co-authors. Update on the profile of the EUSTAR cohort: an analysis of the EULAR

Scleroderma Trials and Research group database. Ann Rheum Dis. 2012 Aug;71(8):1355-60. doi:

10.1136/annrheumdis-2011-200742. Epub 2012 May 21.; IF=9.111;

http://www.ncbi.nlm.nih.gov/pubmed/22615460

Elhai M et al (EUSTAR co-authors), A gender gap in primary and secondary heart dysfunctions in

systemic sclerosis: a EUSTAR prospective study. Ann Rheum Dis. 2014 Oct 23. pii: annrheumdis-2014-

206386. doi: 10.1136/annrheumdis-2014-206386. [Epub ahead of print]; . IF=9.27;

http://ard.bmj.com/content/early/2014/10/31/annrheumdis-2014-206386.short

Maurer B et al, EUSTAR co-authors. Prediction of worsening of skin fibrosis in patients with diffuse

cutaneous systemic sclerosis using the EUSTAR database. Ann Rheum Dis. 2014 Jun 30. pii:

annrheumdis-2014-205226. doi: 10.1136/annrheumdis-2014-205226. [Epub ahead of print]; IF=9.27;

http://ard.bmj.com/content/early/2014/07/07/annrheumdis-2014-205226.short;

http://www.ncbi.nlm.nih.gov/pubmed/24981642

7. EUSTAR Clinical Project IMPRESS 2: International Multi-centric Prospective study on pregnancy in systemic sclerosis, Directori proiect: Monika Ostensen University of Trondheim Norway, Angela Tincani University of Brescia Italy, Antonio Brucato, Ospedale Reuniti Bergamo Italy. oct 2013; aviz 19616/07.10.2013

http://www.eustar.org/ClinicalTrial.html

8. EUSTAR Clinical Project CP11: Prevalence and clinical associations of capillaroscopic scleroderma patterns in the EULAR Scleroderma Trial And Research group (EUSTAR) database of patients with systemic sclerosis. Project Francesca Ingegnoli, (EUSTAR UCN 110), 2011; http://www.eustar.org/ClinicalTrial.html

Ingegnoli F et al (EUSTAR co-authors), Nailfold capillaroscopy in systemic sclerosis: data from the

EULAR scleroderma trials and research (EUSTAR) database. Microvasc Res. 2013 Sep;89:122-8. doi:

10.1016/j.mvr.2013.06.003. Epub 2013 Jun 17.; IF=2.432

http://www.sciencedirect.com/science/article/pii/S0026286213000939

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9. EUSTAR Clinical Project CP14: Biologics in systemic sclerosis patients treated with Rituximab. If you have SSc patients treated with Rituximab; PI O Distler, UCN 006, Zurich; http://www.eustar.org/ClinicalTrial.html

Jordan S, Distler JH, Maurer B, Huscher D, van Laar JM, Allanore Y, Distler O; on behalf of the EUSTAR

Rituximab study group. Effects and safety of rituximab in systemic sclerosis: an analysis from the

European Scleroderma Trial and Research (EUSTAR) group. Ann Rheum Dis. 2014 Jan 17. doi:

10.1136/annrheumdis-2013-204522. [Epub ahead of print]; . IF=9.270;

http://ard.bmj.com/content/early/2014/01/17/annrheumdis-2013-204522.short

10. PROTOCOL IRIS: International Recommendation Implementation Study – a multinational observational study to investigate the impact of recent treatment recommendations for the treatment of patients with rheumatoid arthritis using web-based patient monitoring (METEOR); primary investigator Robert B.M. Landewé (22.05.2013)

Protocol international de monitorizare a pacientului cu PR in cadrul recomandarilor T2T si insertie in registru electronic, cu potential de dezvoltare a multiple publicatii in conditiile analizei multidimensionale a bolii raportat la activitate, calitatea vietii, practice terapeutice.

Membru colectiv national (4)

1. GRANT CNCSIS: Platforma de cercetari fizio-farmacologice si clinice asupra mecanismelor durerii oncologice si non-oncologice; cod CNCSIS 68; Contract 11/15.09.2006; 2006-2008; director proiect OC MUNGIU (membru in echipa de cercetare) (finantare CNCSIS) in cadrul Centrului pentru Studiul si Terapia Durerii de la Universitatea de Medicina si Farmacie "Grigore T. Popa” Iasi;

http://www.umfiasi.ro/Cercetare/CentreDeCercetare/Pages/default.aspx

http://www.algezio.ro/categorie/Cercetare_025/PLATFORMA_DE_CERCETARI_FIZIOFARMACOLOGICE_SI_CLINICE_ASUPRA_MECANISMELOR_DURERII_NONONCOLOGICE_SI_ONCOLOGICE_%28Cod_CNCSIS:_68%29_078.html

proiect de cercetare cu finantare CNCSIS, ce a pus bazele cercetarii aprofundate in domeniul durerii musculoscheletale, cu predilectie durerea inflamatorie, colaborarii interdisciplinare; puncte de reper: infiintarea Centrului de Algeziologie Clinica, achizitie VICON, aparat de analiza computerizata a biomecanicii mersului; grup de studiu dezvoltat ulterior cu activitate si in prezent pe durerea inflamatorie din boala reumatismala cu determinsm imun si insertia terapiei biologice in acest context (sub coordonarea subsemnatei); diseminare rezultate manifestari stiintifice si publicatii ISI;

2. PROIECT POSCCE-A2-O2.2.1-2007-1+Capacitati-I-2007-2, IMPACT IV sesiunea Sept 2007: Centru de cercetare a lupusului eritematos sistemic si bolilor autoimune inrudite (CCLESAI), 2007-2008, proiect finantat (ID 1071); director proiect prof Chirieac R; (director stiintific in echipa proiectului) http://www.poscce.research.ro/ro/articol/1737/fonduri-structurale-istoric-impact-sesiune-impact-iv-septembrie-2007

3. POSCCE A2-O2.2.1-2009-4 Operatiunea 2.2.1 Centru de cercetare a lupusului eritematos sistemic si bolilor autoimune inrudite, Director stiintific, http://www.finantare.ro/stire-15020-Rezultate-preliminare-evaluare-competitia-POS_CCE-A2_O221-_-2009.html (proiect depus la competitia mentionata urmarind dezvoltarea infrastructurii de cercetare pe domeniul lupusului eritematis sistemic; desi punctajul obtinut a situat proiectul intre cele admise, cu un scor egal pentru 4 dintre acestea, nu a beneficiat de finantare)

4. PROIECT POSDRU 81/3.2/S/55648, Formare profesionala pentru implementarea noilor tehnologii in sistemul de sanatate PERFORMED, director proiect – prof dr HD Bolosiu, UMF I Hatieganu Cluj-Napoca, 2010-2013, competitie, fonduri 5.000.000 EURO (realizarea si prezentarea cursuri, Sesiunea de formare NE, http://performed.ro/; http://performed.ro/simpozioane/sesiunea-de-formare-8-nord-est-iasi-10-13-septembrie-2013/

Studii multicentrice, PMOS si de faza II-III (randomizate, controlate)

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Investigator principal PMOS: nationale (4), internationale (10), si trialuri randomizate (9)

1. PROTOCOL ML25228 REPEAT: Studiu observational post-marketing cu Mabthera prescris pacientilor TNF-

IR, pentru evaluarea eficacitatii si sigurantei curelor repetate in practica medicala clinica de rutina

(Repeated Courses in routine Clinical Practice) (2012-2013) sponsor Roche

2. PROTOCOL ML25332 STONE: Studiu observational post-marketing cu Ro-actemra (tocilizumab) prescris

pacientilor DMARD-IR pentru evaluarea eficacitatii si sigurantei adminstrarii in practica clinica de rutina;

sponsor Roche (2009-2011)

3. PROTOCOL ML27953 FAST2 SWITCH: Studiu non-interventional prospective multicentric pentru a evalua

eficacitatea si siguranta rituximab la pacienti cu artrita reumatoida active care au avut un raspuns inadecvat

sau intolerant la un agent anti-TNF (2011) sponsor Roche

4. Protocol ELOCVENT – Evaluarea impactului osteoporozei postmenopauza asupra calitatii vietii pacientelor

– studiu observational sponsor Servier; 04.2008-07.2008

5. PROTOCOL BEL115014 SESAME: Systemic Lupus Erythematosus in CEE Settings: Romania, Poland,

Hungary. An insight on Medical, Economic and Social Burden (2011-2012); sponsor: GSK.

6. PROTOCOL P10-599: An observational study of the impact of the anti-cyclic citrullinated peptide antibody

(anti-CCP) status on the management of patients with early rheumatoid arthritis (study HU-08-02): a multi-

country, multi-center, post-marketing observational study in the routine clinical use (2010-2011); sponsor:

Abbott.

7. PROTOCOL P10-919 EviraEAST: Evaluation of clinical outcome, treatment compliance and tolerability of

Humira (adalimumab) in patients with active Rheumatoid Arthritis, Psoriatic Arthritis and Ankylosing

Spondylitis in Eastern European countries: a multi-country, multicenter post-marketing observational study

in routine clinical use (2009-2011) (PMOS-CE-08-01); sponsor: Abbott.

8. PROTOCOL PMOS P10-733 DEXA: Evaluation of the Role of Adalimumab on extra-articular manifestation-

bone metabolism and bone mineral density in patients with active Rheumatoid Arthritis (2011-2012) (centre

42146); sponsor: Abbott.

9. PROTOCOL P12-768: Multi-country post-marketing observational study on maintenance of effectiveness of

adalimumab (Humira) in patients with ankylosing spondylitis and psoriatic arthritis – a multi-country

observational study in routine use in Central and Eastern Europe (nov 2011-2012 ); sponsor Abbott;

10. PROTOCOL P13-682 IDEA: Impactul adalimumab (Humira) ca terapie asupra utilizării anumitor resurse

legate de îngrijirea sănătății și asupra concediului medical la pacienții cu spondilită anchilozantă, în practica

clinică curentă (2012-2014), sponsor Abbott;

11. PROTOCOL P13‐683 PACE: Evaluarea activitatii fizice la pacientii cu poliartrita reumatoida tratati cu

adalimumab in practica clinica de rutina (PACE)- studiu observational postmarketing, multinational,

multicentric privind practica curentă în Europa Centrală și de Est (2012-2014); sponsor Abbott;

12. PROTOCOL IMM11-0138 ALIGN: Epidemiological/HEOR Study– Multi-country, cross sectionAL study to

determine patient specIfic and General beliefs towards medicatioN and their treatment compliance to

selected systemic therapies in chronic inflammatory diseases (IMID) (2012-2013); sponsor Abbott;

13. PROTOCOL 10297 PROOF: Pacienţi cu spondiloartrită axială: registru multi-naţional al caracteristicilor

clinice, inclusiv progresia radiologică, şi al poverii bolii pe parcursul a 5 ani în condiții reale (2014-2019);

sonsor Abbvie;

14. PROTOCOL IMM-12-0118: Evaluation of management of patients with early rheumatoid arthritis (RA)

in routine clinical practice based on Treat to Target (T2T) principles, (2014-2015), sponsor Abbvie

15. PROTOCOL IM 128-027: Studiu de faza 2 multicentric randomizat dublu orb controlat placebo de evaluate

a sigurantei si eficacitatii BMS-913699 vs placebo adminstrat pe fondul standardelor de ingrijire

restrictionat, ca tratament al subiectilor cu lupus eritematos sistemic active; sponsor Bristoll Myers Squibb

International Corporation Belgia; Investigator Principal (2014)

16. PROTOCOL A3921187 (9002-0249): A Phase 3b/4 randomized double blind study of 5 mg of Tofacitinib

with and without Methotrexate in comparison to Adalimumab with Methotrexate in subjects with moderately

to several active rheumatoid arthritis. Investigator principal (2014)

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17. PROTOCOL G0-VIBRANT. COD CNTO148PSA3001 A multi-centric, randomized, double blind placebo

controlled trial of golimumab, an anti TNF monoclonal antibody, administered intravenously, in subjects with

active psoriatic arthritis. Phase3. Investigator principal (2014)

18. PROTOCOL G0-ALIVE. COD CNTO148AKS3001 A multi-centric, randomized, double blind placebo

controlled trial of golimumab, an anti TNF monoclonal antibody, administered intravenously, in subjects with

active ankylosis spondylitis.Phase3. Investigator principal (2014)

19. PROTOCOL GLASS: A multi-center, randomized double-blind parallel group study on the therapeutic efficacy

and safety of febuxostat (taken once daily) and the therapeutic efficacy and safety of allopurinol on serum

urate concentration in subjects suffering from hyperuricemia and gout (MEIN/11/FEN-Gou/001; CRO

InnoPharma SRL, Sponsor MIOL, 2014-2015

20. PROTOCOL A9391010: a phase 2, randomized, double blind assessment of efficacy and safety of pf-

04171327 (1, 5, 10, 15 mg dose, daily) compared to 5 mg and 10 mg prednisone daily and placebo daily in

subjects with rheumatoid arthritis over an 8 week period followed by a 4 week period of tapering of study

drug; intermediar; Parexel; sponsor: Pfizer; Investigator principal (2014)

21. PROTOCOL B1801315: A randomized, double-blind placebo-controlled study of the maintenance of efficacy

of etanercept plus DMARD(s) compared with DMARD(s) alone in subjects with rheumatoid arthritis after

achieving an adequate response with etanercept plus DMARD(s); CRO: Parexel; sponsor: Pfizer Investigator

principal (2013)

22. PROTOCOL AB 06012: A phase 2b/3 study to evaluate efficacy and safety of masitinib in comparison to

methotrexate in patients with active rheumatoid arthritis with inadequate response to methotrexate or to

any disease-modifying antirheumatic drug; CRO: HT Research RO; sponsor AB Science; Investigator

principal (2013)

23. PROTOCOL PRINT Study, TcLand: Validation study of RA-INF-Dx as multigene molecular in vitro blood test

intended to aid in the identification of patients with rheumatoid arthritis who are unlikely to shown an initial

response to infliximab and methotrexate combination therapy (”Predict non-response to Infliximab therapy

study”) (2011-2012); sponsor: TcLand Expression; CRO: Premier Research Investigator principal (2012);

Subinvestigator (membru in echipa proiectului) sau coordonator de studiu (44)

1. PROTOCOL M12-965 EudraCT 2014-001471-31: Phase 2, Multicenter, Open-Label Extension (OLE) Study

with ABT-122 in Rheumatoid Arthritis Subjects Who Have Completed the Preceding M12-963 Phase 2

Randomized Controlled Trial (RCT) Subinvestigator (2014-in desfasurare); sponsor Abbvie; (Investigator

principal prof Chirieac R) (adeverinta 2/05.01.2015)

2. PROTOCOL EFC 10832: A randomized, double-blind, parallel, placebo-controlled study assessing the efficacy

and safety of sarilumab added to non-biologic DMARD therapy in patients with rheumatoid arthritis who are

inadequate responders to or intolerant of TNF-α antagonists; CRO: Covance; sponsor: Sanofi;

Subinvestigator (2013 – 2014); (Investigator principal prof Chirieac R) (adeverinta 6/05.01.2015)

3. PROTOCOL CD-IA-MEDI-546-1013: A phase 2, randomized study to evaluate the efficacy and safety of

medi-546 in subjects with systemic lupus erythematosus; CRO: INC Research; sponsor: Medimmune;

Subinvestigator (2013 – in desfasurare); (Investigator principal prof Chirieac R) (adeverinta

7/05.01.2015)

4. PROTOCOL CNTO136ARA3002: A study of CNTO 136 (sirukumab), administered subcutaneously, in

patients with active rheumatoid arthritis despite disease-modifying antirheumatic drug (DMARD) therapy

(SIRROUND); CRO: Parexel; sponsor: Janssen; Subinvestigator (2013 – in desfasurare); (Investigator

principal prof Chirieac R) (adeverinta 8/05.01.2015)

5. PROTOCOL RA 0055: A multi-center, randomized, double-blind, placebo-controlled study to evaluate the

efficacy and safety of certolizumab pegol in combination with methotrexate for inducing and sustaining

clinical response in the treatment of DMARD-naïve adults with early active rheumatoid arthritis; CRO:

Parexel; sponsor: UCB Subinvestigator (2013 – 2014); (Investigator principal prof Chirieac R) (adeverinta

9/05.01.2015)

6. PROTOCOL I4V-MC-JADV a randomized, double-blind, placebo and active-controlled, phase 3 study

evaluating the efficacy and safety of baricitinib in patients with moderately to severely active rheumatoid

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arthritis who have had an inadequate response to methotrexate therapy; CRO: ICON; sponsor: Eli Lilly;

Subinvestigator (2013 – in desfasurare); (Investigator principal prof Chirieac R) (adeverinta

10/05.01.2015)

7. PROTOCOL I4V-MC-JADY: a phase 3, multicenter study to evaluate the long-term safety and efficacy of

baricitinb in patients with rheumatoid arthritis; CRO: ICON; sponsor: Eli Lilly; Subinvestigator (2013 – in

desfasurare); (Investigator principal prof Chirieac R) (adeverinta 11/05.01.2015)

8. PROTOCOL H9B-MC-BCDP: a phase 3, multicenter, open label study to evaluate the long-term safety and

efficacy of LY2127399 in patients with Rheumatoid Arthritis; CRO: Quintiles; sponsor Eli Lilly; 2012-2013;

Subinvestigator; (Investigator principal prof Chirieac R) (adeverinta 12/05.01.2015)

9. PROTOCOL H9B-MC-BCDM: a phase 3, multicenter, randomized, double blind placebo controlled study to

evaluate the efficacy and safety of sc LY2127399 in patients with moderate to severe Rheumatoid Arthritis

who had an inadequate response to methotrexate therapy; CRO: Quintiles; sponsor: Eli Lilly;

Subinvestigator (2012-2013); (Investigator principal prof Chirieac R)

10. PROTOCOL H9B-MC-BCDT: a phase 3, multicenter, randomized, double blind placebo controlled study to

evaluate the efficacy and safety of sc LY2127399 in patients with Systemic Lupus Erythematosus; CRO:

Parexel; sponsor: Eli Lilly; Subinvestigator (2012-2013); (Investigator principal prof Chirieac R)

(adeverinta 13/05.01.2015)

11. PROTOCOL H9B-MC-BCDO: a phase 3, multicenter, randomized, double blind placebo controlled study to

evaluate the efficacy and safety of sc LY2127399 in patients with Rheumatoid Arthritis with or without

background of Disease Modifying Anti-Rheumatic Drug(DMARD) therapy; CRO: Quintiles; sponsor: Eli Lilly;

Subinvestigator (2012-2013); (Investigator principal prof Chirieac R) (adeverinta 14/05.01.2015)

12. PROTOCOL H9B-MC-BCDX: a phase 3b, multicenter, open-label study to evaluate the long-term safety and

efficacy of subcutaneous LY2127399 in patients with systemic lupus erythematosus (SLE) (illuminate-x); CRO:

Parexel; sponsor: Eli Lilly; Subinvestigator (2012-2013); (Investigator principal prof Chirieac R)

(adeverinta 15/05.01.2015)

13. PROTOCOL Novartis CAIN457F2306: A randomized double-blind placebo-controlled multicenter study,

Novartis, Subinvestigator (2012-2013); (Investigator principal prof Chirieac R)

14. PROTOCOL WA22762: A randomized, double-blind, parallel group study of the safety and effect on clinical

outcome of tocilizumab SC versus tocilizumab IV, in combination with traditional disease modifying anti-

rheumatoid arthritis drugs (DMARDs), in patients with moderate to severe active rheumatoid arthritis; CRO:

Comac sponsor Hoffman La Roche, Sub-investigator, 2010 -2104; Subinvestigator(Investigator principal

prof Chirieac R) (adeverinta 16/05.01.2015)

15. PROTOCOL ENTRACTE: A clinical outcomes study to evaluate the effects of IL-6 receptor blockade with

tocilizumab (TCZ) in comparison with etanercept (ETA) on the rate of cardiovascular events in patients with

moderate to severe rheumatoid arthritis (RA);CRO: Quintiles; sponsor : Hoffmann-LaRoche, Subinvestigator,

(Investigator principal prof Chirieac R) (2012- in desfasurare) (adeverinta 17/05.01.2015)

16. PROTOCOL I4V-MC-JADA: A randomized, double blind placebo controlled, dose ranging, parallel group,

phase 2b study in patients with active RA on MTX background therapy spondor: Eli Lilly; CRO Parexel; Sub-

investigator, 2010 - 2014 (Investigator principal prof Chirieac R) (adeverinta 18/05.01.2015)

17. PROTOCOL Protocol I1F-MC-RHAK: studiu faza II cu doze variabile, subcutanate multiple de LY2439821

(Ac anti IL-17) la pacienti cu artrita reumatoida activa care urmeaza tratament concomitent cu DMARD;

sponsor: Eli Lilly; Sub-investigator, 2010 - 2013 (Investigator principal prof Chirieac R) (adeverinta

19/05.01.2015)

18. PROTOCOL A phase II, randomized, double-blind, controlled study to evaluate the immune responses, safety

and clinical efficacy of three doses of Neovacs’ TNF Kinoid in adult patients with rheumatoid arthritis who

have relapsed despite anti-TNF- biological therapy-sponsor Neovasc; CRO Genexion, Sub-investigator,

2010 - 2011

19. PROTOCOL P06129 GO-MORE: Un studiu cu design deschis (open-label),pentru a evalua adaugarea de

Golimumab Subcutanat (GLM) la terapia conventionala cu medicamente modificatoare de boala (DMARD) la

pacientii cu Artrita Reumatoida naivi la terapia biologica (Partea 1) urmata de un studiu randomizat ce

evalueaza valoarea terapiei combinate cu GLM administrat intravenous si subcutanat in scopul inducerii si

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mentinerii remisiunii(Partea 2); MSD, Sub-investigator, 2010 – 2012 (Investigator principal prof Chirieac

R) (adeverinta 20/05.01.2015)

20. PROTOCOL TRU-015-3206K1-2203-WW: a randomized, parallel, double-blind, placebo controlled dose

regimen finding study to evaluate the safety and efficacy of TRU-015 in subjects with active seropositive

Rheumatoid Arthritis on a stable background of methotrexate; sponsor & CRO: Wyeth; Sub-investigator,

2009-2011 ; (Investigator principal prof Chirieac R)

21. PROTOCOL A3921024: A long term, open label follow up study of CP-690.550, a moderately selective Janus

kinase 3 inhibitor, for treatment of Rheumatoid Arthritis. Sponsor & CRO: Pfizer; Sub-investigator, 2009-in

desfasurare (Investigator principal prof Chirieac R) (adeverinta 21/05.01.2015)

22. PROTOCOL RADAR: PROTOCOL P05320, Observational Trial on the value of diagnostic criteria in the diagnosis of spinal spondylarthropathies in patients with chronic low back pain; Recognizing and

Diagnosing Ankylosing Spondylitis Reliably; sponsor MSD; Sub-investigator, 2009-2010 (Investigator

principal prof Chirieac R) (adeverinta 22/05.01.2015)

23. PROTOCOL BT971: studiu randomizat, controlat placebo, dublu orb cu esaladarea dozei pentru a evalua

eficacitatea, siguranta, si tolerabilitatea medicatiei de studiu BT971 la pacienti cu artrita reumatoida cu

tratament concomitent cu MTX; sponsor: Biotest AG Germany; CRO: IFE Romania, Sub-investigator, 2009-

2010 ; (Investigator principal prof Chirieac R) (adeverinta 23/05.01.2015)

24. PROTOCOL H8C-MC-LQBG: A Phase 2 Study of the Effects of LY545694, an iGluR5 Antagonist, in the

Treatment of Subjects With Osteoarthritis Knee Pain; sponsor: Eli Lilly; Sub-investigator, 2008-2009;

(Investigator principal prof Chirieac R) (adeverinta 24/05.01.2015)

25. PROTOCOL WA20496: A randomized, double-blind, parallel group, international study to evaluate the

safety and efficacy of Ocrelizumab given as a single infusion or dual infusion compared with placebo in

patients with active Rheumatoid Arthritis who have an inadequate response to methotrexate therapy;

Sponsor: Hoffmann La Roche; CRO: Quintiles Romania; subinvestigator, 2008-2011; (Investigator

principal prof Chirieac R) (adeverinta 25/05.01.2015)

26. PROTOCOL ROB 803-09-002: a phase II, randomized, double-blind, multicenter placebo-controlled, dose-

ranging, parallel study group to evaluate the efficacy and safety of orally administered Rob 803 when added

to stable MTX in patients with moderate or severe active Rheumatoid Arthritis; Sponsor: Oxypharma; CRO:

Pharm-Olam; Sub-investigator, 2008-2009 ; (Investigator principal prof Chirieac R) (adeverinta

26/05.01.2015)

27. PROTOCOL LJP 394-90-14: A randomized, double-blind, placebo controlled, three arm, parallel group,

multicenter, multinational safety and efficacy trial of 300 mg and 900 mg of Abetimus Sodium in SLE patients

with a history of renal disease; sponsor: La Jolla International; CRO: Pharm-Olam; subinvestigator, 2008-

2009; (Investigator principal prof Chirieac R) (adeverinta 27/05.01.2015)

28. PROTOCOL WA20499: A randomized, double-blind placebo controlled parallel group multicenter study to

evaluate the efficacy and safety of two doses of Ocrelizumab in patients with active SLE; Sponsor: Hoffmann-

La Roche Ltd/ Genetech Inc; CRO: Quintiles Romania, subinvestigator, 2008-2009; (Investigator principal

prof Chirieac R) (adeverinta .01.2015)

29. PROTOCOL IP-004: studiu faza IIb, multicentric, randomizat, dublu orb, placebo-contolat pentru evaluarea

sigurantei, tolerantei si eficacitatii a doua doze de studiu IPP 201101 subcutanat plus terapia standard, in

comparatie cu placebo la pacientii cu LES; sponsor: Immupharma; CRO: Genexion; Sub-investigator, 2008-

2009 ; (Investigator principal prof Chirieac R) (adeverinta 28/05.01.2015)

30. PROTOCOL A3921035: a phase II B, randomized, double blind, placebo controlled active comparator,

multicenter study to compare 5 dose regiments of CP-690.550 and adalimumab versus placebo, administered

for 6 months in the treatment of subjects with active Rheumatoid Arthritis. Sponsor & CRO: Pfizer, Sub-

investigator, 2008-2009 ; (Investigator principal prof Chirieac R) (adeverinta 29/05.01.2015)

31. PROTOCOL D1520C00001: a randomized, double-blind (with open comparator Etanercept), placebo-

controlled, phase IIB multicenter study to evaluate the efficacy of 4 doses of AZD9056 administered for 6

months on the signs and symptoms of Rheumatoid Arthritis in patients with active disease receiving

background MTX or Sulphasalasine; sponsor: Astra-Zeneca; CRO: Verum; Sub-investigator, 2008-2009 ;

(Investigator principal prof Chirieac R) (adeverinta 30/05.01.2015)

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32. PROTOCOL MDX 1100-04: a phase II, multi-dose, double-blind, placebo controlled, randomized, multicenter

study of MDX-1100 (anti CXCL 10 Human Monoclonal Antibody) in patients with active Rheumatoid Arthritis;

sponsor: Medarex; CRO: PSI Pharma; Sub-investigator, 2008-2009; (Investigator principal prof Chirieac

R) (adeverinta 31/05.01.2015)

33. PROTOCOL ACT5488: Activity and safety of oral administration of SSR150106XB for the reduction of

inflammation in patients with active rheumatoid arthritis; :a 4 week, multicenter, randomized, double-blind,

placebo-controlled parallel group study of 90 mg administered once daily and 90mg once every other day;

Sponsor Sanofi-Aventis; CRO: I3 research; subinvestigator, 2007-2008; (Investigator principal prof

Chirieac R) (adeverinta 32/05.01.2015)

34. PROTOCOL P04422: A randomized, multicenter, international open label study of infliximab plus

methotrexat versus methotrexat alone for the treatment of methotrexate naive subjects with active psoriatic

arthritis; sponsor & CRO: Schering Plough Central East AG; faza IV; subinvestigator, 2007-2008;

(Investigator principal prof Chirieac R) (adeverinta 33/05.01.2015)

35. PROTOCOL: A phase 2 multicenter randomized double-blind placebo-controlled parallel-group dose finding

study of the safety and efficacy of daily CF101 administered orally when added to weekly methotrexate in

patients with active rheumatoid arthritis; Sponsor Can-fite Bio-Pharma Ltd; CRO: Pharm Olam

International; subinvestigator 2006-2007; (Investigator principal prof Chirieac R) (adeverinta

37/05.01.2015)

36. PROTOCOL WA17047: A randomized, phase 3, controlled, double-blind, parallel-group, multicenter study to

evaluate the safety and efficacy of rituximab in combination with methotrexat compared to methotrexate

alone, in methotrexat –naïve patients with active rheumatoid arthritis; Sponsor: Hoffmann-La Roche

Genentech; CRO: Parexel, subinvestigator 2006-2010; (Investigator principal prof Chirieac R) (adeverinta

36/05.01.2015)

37. PROTOCOL P1-0205: Efficacy and safety of FASU1 versus FASU2 in a 180 day study treatment in patients

with osteoarthritis of the knee; Sponsor Laboratoires Expascience; CRO: CRC Pharmaceuticals,

subinvestigator 2006-2007; (Investigator principal prof Chirieac R) (adeverinta 35/05.01.2015)

38. PROTOCOL F1J-MC-HMEP. Duloxetine 60 to 120mg versus placebo in the treatment of patients with

Osteoarthritis knee pain; sponsor si CRO: Eli Lilly Romania SRL; subinvestigator 2006-2007; (Investigator

principal prof Chirieac R)

39. PROTOCOL D1520C05287. A randomized double-blind, placebo-controlled, parallel group, ascending dose

study to assess the activity, safety and tolerability of 2 doses of AZD9056 for 4 weeks in patients with active

rheumatoid arthritis receiving methotrexate and/or sulphasalazine, phase II; sponsor Astra Zeneca; CRO

Parexel International SRL, subinvestigator, 2005-2006; (Investigator principal prof Chirieac R)

(adeverinta 34/05.01.2015)

40. PROTOCOL MDT3-005. A two-arm study comparing the analgesic efficacy and safety of Tramadol HCl once-

a-day versus placebo for the treatment of pain due to osteoarthritis of the knee; CRO: Parexel International;

coordonator studiu, 2005-2006; (Investigator principal prof Chirieac R) (adeverinta 38/05.01.2015)

41. PROTOCOL H4Z-MC-GJAD. Effects of Arzoxifene on vertebral fracture incidence and on invasive breast

cancer incidence in postmenopausal; women with osteoporosis or with low bone density; Sponsor Ely Lilly

and Company; CRO: Quintiles Romania; subinvestigator, 2004-2009; (Investigator principal prof Chirieac

R) (adeverinta 39/05.01.2015)

42. PROTOCOL MI-CP100: A phase II, randomized, double -blind study to evaluate the effects of MEDI-522, a

humanized monoclonal antibody to integrin alpha V beta 3 on disease activity and progression of joint

damage in patients with active rheumatoid arthritis sub-optimally responding to methotrexat; sponsor

Medimmune; CRO: PSI Pharma Support Romania SRL; coordonator studiu, 2003-2004; (Investigator

principal prof Chirieac R)

43. PROTOCOL Studiu multicentric, de faza III, randomizat, asupra tolerabilitatii Tramadol la pacienti cu atroza

de genunchi; Parexel International, coordonator studiu, 2003-2004; (Investigator principal prof Chirieac

R)

44. PROTOCOL Studiu multicentric, de faza III, randomizat, dublu orb, placebo-controlat asupra tolerabilitatii

gastro-intestinale a combinatiei terapeutice diclofanac-misoprostol (ArthrotecR) la pacienti cu atroza de

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genunchi; coordonator studiu, 1998-1999; (Investigator principal prof Chirieac R) (adeverinta

40/05.01.2015)

Burse de tip mobilitate pentru pregatire profesionala, obtinute prin competitie (evaluarea CV, scrisoare de motivatie)

3rd Annual Meeting of the Lupus Academy, 7-9 March 2014 Berlin, Germany (bursa)

14th EULAR Intermediate Sonography Course, 10-13 June 2007, Sitges, Barcelona, Spania (bursa studiu EULAR)

9th EULAR Sonography Course (from introductory to advanced practical course on musculoskeletal sonograhy), 9-12 Dec 2004, Paris, France (bursa de studiu EULAR);

1st European Course–Capillaroscopy and Rheumatic Diseases, 10-12 Sep 2004, Genova, Italy (bursa EULAR);

6th EULAR Postgraduate Course in Rheumatology, 18-27 June 2000, Nice, Franta (sub patronaj EULAR) (bursa de studiu EULAR);

Lucrari de diploma indrumate: 74 lucrari licenta Facultatea de Medicina (42 licenta in limba engleza); 14 lucrari indrumate Faculatatea Bioinginerie; 3 lucrari in dubla coordonare cu cadru didactic disciplina Ergonomie, Facultatea Stomatologie (web-site-ul bibliotecii UMF “Gr.T.Popa” Iasi)

Proiecte educationale si de formare medicala continua

IASP Grant: Musculoskeletal pain academy, 2011, IASP Developing Countries Project: Initiative for

improving pain education; jul2011-jul2012; (acord UMF “Gr.T.Popa” Iasi nr.12119/28.06.2011);

finantare IASP 7000 USD; (coordonator international)

IASP Grant IASP Developing Countries Project: Initiative For Improving Pain Education - Grant IASP

(International Association for the Study of Pain); Manager de proiect dr. Jaba Irina 05.2009-05.2010;

(accord UMF Iasi 8499/20.05.2009); finantare IASP 9700 USD, membru in echipa

Cursuri postuniversitare EMC acreditate, Facultatea Medicina, UMF Gr.T.Popa Iasi – Coordonator (6)

An universitar 2014/2015, http://www.umfiasi.ro/EMC/Documents/cursuri%20postuniversitare%202014-

2015/medicina%202014%202015.pdf

1. Sclerodermia sistematică (SS) – aspecte practice clinice şi terapeutice, 01.03-30.04.2015

An universitar 2010/2011 ( http://www.umfiasi.ro/EMC/EMC/EMC_Medicina_2010-2011.pdf)

2. Terapia biologica in boli inflamatorii cronice cu determinism imun, 1-31 mar 2011

3. Evaluare si monitorizare in bolile reumatismale inflamatorii cornice, 1-28 feb 2011

4. Sclerodermia sistemica (SS) – actualitati diagnostice si terapeutice, 1-30 apr 2011,

An universitar 2009/2010

5. Evaluare si monitorizare in bolile reumatismale inflamatorii cornice, 1-28 feb 2010

6. Sclerodermia sistemica (SS) – actualitati diagnostice si terapeutice, 1-30 apr 2010

Proiecte de educatie continua nationale (membru) (4)

PROIECT POSDRU 81/3.2/S/55648, Formare profesionala pentru implementarea noilor tehnologii

in sistemul de sanatate PERFORMED, director proiect – prof dr HD Bolosiu, UMF I Hatieganu Cluj-

Napoca, 2010-2013, competitie, fonduri 5.000.000 EURO, membru cu participare directa in realizarea si

prezentarea cursuri, Sesiunea de formare NE, http://performed.ro/;

http://performed.ro/simpozioane/sesiunea-de-formare-8-nord-est-iasi-10-13-septembrie-2013/

Master UMF Gr.T.Popa Iasi, specializarea Boli cu determinism imun, coordonator prof. univ dr Rodica

Marieta Chirieac (mai 2006-dec 2007); lector;

Tulburari de crestere staturo-ponderala, coordonator prof dr. Corina Galesanu; lector; (syllabus ISBN

978-973-7682-11-6), curs postuniverstar acreditat UMF Iasi, An universitar 2006/2007

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Boli osoase endocrine-metabolice; coordonator prof dr C Galeasanu; lector

Lector cursuri postuniversitare formare continua (23)

1. Curs Osteoporoza (de la diagnostic la tratament) o provocare pentru practician, 28 feb-02 mar2013

Iasi, Romania, coordonator prof dr. Corina Galesanu; lector (Osteoporoza glucocorticoid indusa;

Osteoporoza la barbat)

2. Curs postuniversitar (Rolul medicului de familie in diagnosticarea, monitorizarea si managementul

poliartritei reumatoide, Lector, Conferinta Zilele Spitalului Clinic de Recuperare 3-7 apr 2012,

3. Conferinta Zilele Spitalului Clinic de Recuperare 3-7 apr 2012, Iasi, Romania; Manifestarile

cardiovasculare din bolile reumatismale imunoinflamatorii cronice: screening, diagnostic si management",

curs interdisciplinar Cardiologie-Reumatologie; lector (Hipertensiunea arteriala pulmonara in contextul

bolilor reumatismale: date epidemiologice, etiopatogenie, diagnostic clinic);

4. Curs EMC: Urgențe reumatologice în practica clinică, Conferinta ”Zilele Spitalului Clinic de Recuperare”

(editia a IX-a), 22-27 mar 2011, Iasi, Romania: Impactul recuperarii asupra calitatii vietii; lector (Criza

renala sclerodermica)

5. Curs postuniversitar: Dizabilitatea și calitatea vieții în bolile reumatismale cronice, Conferinta

“Zilele Spitalului Clinic de Recuperare” (editia a IX-a), 22-27 mar 2011, Iasi, Romania: Impactul recuperarii

asupra calitatii vietii. Lector (Poliartrita reumatoida, dizabilitatea si calitatea vietii)

6. Curs postuniversitar Reumatologie, 15-16 apr 2010, Iasi, Romania. Coordonator prof Chirieac R;

lector (Evaluarea – clinica, functionala, de calitate a vietii in poliartrita reumatoida; Posibile ratiuni clinice

pentru ciclizarea tratamentului anti-TNF; switching si efecte adverse)

7. Curs postuniversitar: Osteoporoza – boala cronica invalidanta. De la depistarea precoce la

tratament, 20 mar 2010, Iasi, Romania. Coordonator curs: prof Galesanu C, moderatori sesiune: prof

Galesanu C, prof Botez P; lector (Osteoporoza glucocorticoid indusa. Poliartrita reumatoida)

8. Curs postuniversitar: Osteoporoza – Aspecte teoretice si practice, Conferinta “Zilele Spitalului Clinic

de Recuperare” (editia a VII-a), 24-28 mar 2009, Iasi, Romania: Actualitati in preventia si recuperarea

medico-chirurgicala; coordonator prof dr. Rodica Chirieac; lector (Modalitati diagnostic in osteoporoza–

evaluarea DXA; Actualitati in managementul osteoporozei– medicatia antiosteoporotica cu actiune duala;

Actualitati in managementul osteoporozei – perspective terapeutice in osteoporoza; Monitorizarea terapeii

anti-osteoporotice

9. Curs postuniversitar: Performantele musculare si rolul in reeducarea functional din bolile

reumatismale, neurologice, cardio-vasculare, posttraumatice Conferinta “Zilele Spitalului Clinic de

Recuperare” (editia a VII-a), 24-28 mar 2009, Iasi, Romania: Actualitati in preventia si recuperarea medico-

chirurgicala; lector (Metode de reabilitare: metode electrice–stimularea electrica neuromusculara; Metode

de reabilitare: metode kinetoterapeutice – tehnici de facilitare; Particularitati ale muschiului si metode de

recuperare in boli reumatismale: poliartrita reumatoida, miopatii de tip inflamator, artroza)

10. Curs postuniversitar: Recuperarea medicala si reabilitarea – un act terapeutic de echipa;

coordonator: dr Gavrilas C. Manifestarea “Zilele Spitalului de Recuperare “Sf Gheorghe” Botosani”, 23-24

apr 2008, Botosani, Romania (editia I); Lector

Chirieac R, ANCUTA C, Tacu C, Gavrilas C, Recuperarea medicala si reabilitarea intre present si viitor, aspect ale

interdisciplinaritatii, Modul Recuperare; Rezus E, Chirieac R, ANCUTA C, Tacu C, Recuperarea soldului operat,

Modul Recuperare; ANCUTA C, Tacu C, Rezus E, Tehnici de facilitare in recuperare, Modul Recuperare; Rezus E,

Chirieac R, ANCUTA C, Tehnica exercitiului aerobic, modul Recuperare; Chirieac R, ANCUTA C, Gavrilas C, Evaluarea

clinica in poliartrita reumatoida si impactul pe reeducarea functionala, modul Reumatologie; ANCUTA C, Rezus E,

Gavrilas C, Evaluarea si monitorizarea tratamentului in bolile reumatismale inflamatorii cronice, modul

Reumatologie; Rezus E, Chirieac C, ANCUTA C, Evaluarea in osteoporoza, modul Reumatologie;Chirieac R, ANCUTA

C, Rezus E, Mecanismele durerii, modul Algeziologie; Rezus E, Chirieac R, ANCUTA C, Durerea din afectiunile

degenerative, modul Algeziologie; Ancuta Codrina, Chirieac R, Durerea de tip inflamator, modul Algeziologie

11. Curs postuniversitar: Bio-Care – terapie revolutionara in bolile autoimune: actualitati si

perspective (coordonator R. Chirieac), Conferinta “Zilele Spitalului Clinic de Recuperare Iasi, 20-22 mar

2008, Iasi, Romania; lector (Efecte adverse ale terapiei biologice. Infectia tuberculoasa – screening si

monitorizare; Terapia anti-CD20)

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12. Curs postuniversitar: Actualitati in imunopatologia si terapia bolilor reumatismale cu determinism

imun, Conferinta “Zilele Spitalului Clinic de Recuperare Iasi” (editia a V-a), 29-31 mar 2007, Iasi, Romania;

lector

13. Curs postuniversitar: Exercitiu aerobic: implicatii teoretice si practice, Conferinta “Zilele Spitalului

Clinic de Recuperare Iasi” (editia a V-a), 29-31 mar 2007, Iasi, Romania; lector

14. Curs EMC: Managementul durerii in patologia reumatismala, 25 mai 2007, Iasi, Romania moderator

prof Chirieac R; Lector (Managementul durerii articulare in reumatismele inflamatorii

15. Curs EMC: 05 Dec 2007, Suceava, Romania; moderator prof Chirieac R; Lector, Terapii eficiente in

patologia musculoscheletala.

16. Curs postuniversitar: Terapia prin miscare. Aspecte fiziopatologice si practice, Conferinta “Zilele

Spitalului Clinic de Recuperare Iasi” (editia a IV-a), 6-8 apr 2006, Iasi, Romania;

R Chirieac, ANCUTA C, C Munteanu, Recuperarea aparatului musculo-scheletal; R Chirieac, L Macovei, I Boaru, C Tacu,

ANCUTA C, Parametrii fizici ai miscarii; R Chirieac, ANCUTA C, C Nacu, Metode practice de intretinere si recuperare a

miscarii: mobilitate, flexibilitate, ROM, posturari; ANCUTA C, C Tacu, Tehnici de facilitare

17. Curs EMC: Managementul bolii artrozice. Curs pentru depistarea, diagnosticarea precoce si

tratamentul bolii artrozice, 2006, Bacau, Romania. Lector, Terapia bolii artrozice si rolul coxibilor.

18. Curs EMC: Managementul bolii artrozice. Curs pentru depistarea, diagnosticarea precoce si

tratamentul bolii artrozice, 14 apr 2006 Suceava, Romania, lector, Boala artrozica – prezentare de caz

19. Curs EMC: Managementul bolii artrozice. Curs pentru depistarea, diagnosticarea precoce si

tratamentul bolii artrozice, 2006, Iasi, Romania, Lector, Boala artrozica – prezentare de caz

20. Curs EMC: Eficacitatea – obiectiv esential in tratamentul afectiunilor musculo-scheletale, 3 mar

2006, Iasi, Romania, coordonatori – prof dr. Chirieac R, ptof dr. Bolosiu H, lectori: Ionescu R, Balanescu A,

ANCUTA C, Rezus E, sarbu P

21. Curs EMC: Osteoporoza- o epidemie cu adevarat silentioasa?, 05 nov 2005, Iasi, Romania; moderator

Sirbu P, participant: Sirbu P, ANCUTA C (Fracturile vertebrale: cause declansatoare si preventia acestora),

Branisteanu D, Galesanu C (5 EMC)

22. Curs EMC: Patologia osteoarticulara la inceput de mileniu, 27 apr 2004, Iasi, Romania moderatori: prof

Chirieac R, Bolosiu H; ANCUTA C, Tratamentul biologic al afectiunilor cronice inflamatorii.

23. Curs EMC: Calitatea vietii virstnicului cu afectiuni musculo-scheletale, 26 nov 2003, Iasi, Romania,

moderator prof Chirieac R, lectori: prof Pandele G, conf Botez P, Rezus E, ANCUTA C (Caractere clinico-

patogenice, terapeutice si calitatea vietii varstnicului cu poliartrita reumatoida).

Membru in comitete științifice, organizator de manifestări științifice (18)

1. Organizator/coordonator Workshop – Poliartrita reumatoida – de la diagnostic la tratament – ANCUTA C,

Bojinca M, Ancuta I, Conferinta Zilele Spitalului Clinic de Recuperare Iasi, 25-29 mar 2014, Iasi, Romania,

2. Organizator/ coordonator Workshop, Artropatiile microcristaline: o noua abordare patogenica, diagnostica

si terapeutica, Conferinta Zilele Spitalului Clinic de Recuperare Iasi, 25-29 mar 2013, Iasi, Romania

3. Comitet de organizare Conferinta Zilele Spitalului Clinic de Recuperare Iasi, 26-29 mar 2013, Iasi, Romania

4. Comitet de organizare/ Coordonator modul Reumatologie II: Autoimunitatea la pacientul varstnic:

particularitati de diagnostic si terapie; Conferinta Zilele Spitalului Clinic de Recuperare Iasi – editia XI, 26-29

mar 2013, Iasi, Romania

5. Comitet de organizare Conferinta Zilele Spitalului Clinic de Recuperare Iasi, 3-7apr 2012, Iasi, Romania

6. Congresul Roman de Reumatologie 23-26 nov 2011; Brasov, Romania

7. Comitet de organizare Congresul Roman de Reumatologie, 19-22 oct 2010, Brasov, Romania

8. Comitet de organizare Conferinta Zilele Spitalului Clinic de Recuperare Iasi (editia a VIII-a), 23-27 mar 2010,

Iasi, Romania

9. Comitet de organizare Conferinta Zilele Spitalului Clinic de Recuperare Iasi (editia a VII-a), 24-28 mar 2009,

Iasi, Romania

10. Comitet de organizare Coferinta Zilele Spitalului Clinic de Recuperare Iasi, Editie aniversara 30 ani, 20-22

martie 2008

11. Congresul National de Reumatologie cu participare internationala, 14-17 sep 2005, Brasov, Romania

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12. Conferinta Zilele Spitalului Recuperare 27-29 mar 2003, Iasi, Romania

13. Conferinta Nationala de reumatologie cu participare internationala, Iasi, 28-30 mai 1998

14. Consiliul stiintific al XXI-lea Congres National de Reumatiologie, 1-4 Oct 2014, Bucuresti

15. Comitet stiintific Conferinta Zilele Spitalului Clinic de Recuperare Iasi editia a XII-a, 25-29 Martie 2014,

Iasi, Romania

16. Comitet stiintific al XX-lea Congres National de Reumatologie 25-28 sept 2013, Bucuresti,

17. Comitet stiintific – Zilele Spitalului de Recuperare Sf Gheorghe Botosani, editia 1, 23-24 apr 2008, Botosani,

Romania

18. Secretar stiintific Congresul National OSART, 14-17 mai 2008, Iasi, Romania

Brevete de inventie: 2 internationale (vezi lista completa de lucrari anexata)

Evaluare activitate didactica si cercetare anuala – in primele 10 locuri din universitate in ultimii 3 ani (http://www.umfiasi.ro/Pages/Default.aspx)

Nume si adrese contact personalitati din domeniu pentru recomandare

Professor Ariane HERRICK, professor of Rheumatology, University of Msnchester, UK, Telephone +44

(0)161 275 5993; Email: [email protected] (recomandare atasata)

Prof univ dr. Mioara BANCIU, Email: [email protected], mobil 0744925789Timisoara, Romania

(recomandare atasata)

Prof univ dr. Maria SUTA, Email: [email protected]; mobil: 0723213019, Constanta, Romania

(recomandare atasata)

Conf univ dr. Denisa PRESETEANU, Email: [email protected]; mobil 0723640548, Bucuresti, Romania

(recomandare atasata)

Prof univ dr Laurentiu MOGOANTA, Email: [email protected], Craiova, Romania,

(recomandare atasata)

Prof univ Eugen CARASEVICI, Iasi, Romania, Email: [email protected]

Prof univ dr Minodora MAZUR, Chisinau, Moldova, email: [email protected]

Prof univ dr Liliana GROPPA, Chisinau, Moldova, email: [email protected]

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Recunoasterea contributiilor stiintifice: (272 citari) (254 citari in reviste cotate ISI)

Adresa web pt citari: http://scholar.google.ro/scholar?start=50&q=codrina+ancuta&hl=ro&as_sdt=0,5

http://scholar.google.ro/scholar?q=ancuta+c&btnG=&hl=ro&as_sdt=0%2C5

Articol citat: A phase II, randomized, double‐blind, placebo‐controlled study evaluating the efficacy and safety

of MDX‐1100, a fully human anti‐CXCL10 monoclonal …, …, H LeBlanc, G Nichol, C Ancuta… - Arthritis & …,

2012 - Wiley Online Library

1. B cells as therapeutic targets in SLE, I Sanz et al, Nature Reviews Rheumatology, 2010 - nature.com,

2. Chemokines: established and novel targets in atherosclerosis, RR Koenen et al, EMBO molecular medicine,

2011 - embomolmed.embopress.org

3. Innovative therapies for systemic sclerosis, VH Ong, CP Denton, Current opinion in rheumatology, 2010 -

journals.lww.com

4. Trial Watch, L Zitvogel, G Kroemer - 2012 - landesbioscience.com, [HTML] from nih.gov (CITARE BDI)

5. CXCL10 and its receptor CXCR3 regulate synovial fibroblast invasion in rheumatoid arthritis, T Laragione et

al, Arthritis & …, 2011 - Wiley Online Library

6. Synoviocyte innate immune responses: TANK-binding kinase-1 as a potential therapeutic target in

rheumatoid arthritis, D Hammaker et al, Rheumatology, 2012

7. B cell therapies for rheumatoid arthritis: beyond B cell depletion, I Calero et al, Rheumatic Disease Clinics of

North America, 2010 – Elsevier

8. International Union of Basic and Clinical Pharmacology. LXXXIX. Update on the Extended Family of

Chemokine Receptors and Introducing a New Nomenclature for …, F Bachelerie et al, Pharmacological …,

2014 – ASPET,

9. Rheumatoid arthritis therapy: advances from bench to bedside, SI Choi, E Brahn, Autoimmunity, 2010

10. Anti-IP-10 antibody (BMS-936557) for ulcerative colitis: a phase II randomised study, L Mayer et al, Gut,

2014

11. Enhanced expression of CXCL10 in inflammatory bowel disease: Potential role of mucosal toll‐like receptor 3

stimulation, AE Østvik et al, Inflammatory bowel …, 2012 - Wiley Online Library

12. Chemokine (C–X–C motif) ligand (CXCL) 10 in autoimmune diseases, A Antonelli et al, Autoimmunity …, 2014

– Elsevier

13. The interaction between CXCL10 and cytokines in chronic inflammatory arthritis, EY Lee, ZH Lee, YW Song -

Autoimmunity reviews, 2013 – Elsevier

14. Targeting chemokines and chemokine receptors with antibodies, A Klarenbeek et al, Drug Discovery Today:

…, 2013 – Elsevier

15. Liver X receptor regulates rheumatoid arthritis fibroblast-like synoviocyte invasiveness, matrix

metalloproteinase 2 activation, interleukin-6 and CXCL10, T Laragione, PS Gulko, Molecular Medicine, 2012

16. Monoclonal antibody against CXCL-10/IP-10 ameliorates influenza A (H1N1) virus induced acute lung injury,

W Wang et al, Cell …, 2013 - ncbi.nlm.nih.gov, [HTML] from nature.com

17. Safety and Efficacy of the Newer Biological Therapeutics in the Treatment of Rheumatoid Arthritis, V

Navarro-Compán… - Clinical Medicine Insights …, 2011

18. Emerging therapies for rheumatoid arthritis, P Jacques, F Van den Bosch, Expert opinion on emerging …,

2013

19. Prolonged TNFα primes fibroblast‐like synoviocytes in a gene‐specific manner by altering chromatin, C Sohn

et al, Arthritis & …, 2014 - Wiley Online Library

20. Review: new anti-cytokines for IBD: what is in the pipeline?, M Scharl, SR Vavricka, G Rogler, Current drug

targets, 2013 - ingentaconnect.com

21. The JAK inhibitor tofacitinib suppresses synovial JAK1-STAT signalling in rheumatoid arthritis, DL Boyle et al,

Annals of the …, 2014 - ard.bmj.com

22. Перспективы фармакотерапии ревматоидного артрита: моноклональные антитела, ЕЛ Насонов, ЛН

Денисов… - Научно-практическая …, 2012 - cyberleninka.ru

23. Thymidine Phosphorylase Regulates the Expression of CXCL10 in Rheumatoid Arthritis Fibroblast‐like

Synoviocytes, Y Toyoda et al, Arthritis & …, 2014 - Wiley Online Library

24. Chemokines and chemokine receptors blockers as new drugs for the treatment of chronic obstructive

pulmonary disease, G Caramori et al, Current medicinal …, 2013 - ingentaconnect.com

25. Brief Report: Inadequate Description and Discussion of Enrolled Patient Characteristics and Potential Inter–

Study Site Differences in Reports of Randomized …, S Yurdakul et al, Arthritis & …, 2014 - Wiley Online

Library

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26. Targeting Chemokine (CXC motif) Receptor 3 in Thyroid Autoimmunity, P Fallahi et al, Recent patents on …,

2014 - ingentaconnect.com

27. Inflammatory cytokines epigenetically regulate rheumatoid arthritis fibroblast-like synoviocyte activation by

suppressing HDAC5 expression, C Angiolilli et al, Annals of the …, 2014 - ard.bmj.com

28. Novel treatment options for ulcerative colitis, BP Vaughn, AC Moss - Clinical investigation, 2013 - Future

Science

29. Anti-inflammatory drimane sesquiterpene lactones from an< i> Aspergillus</i> species, S Felix et al,

Bioorganic & medicinal chemistry, 2014 – Elsevier

30. World Journal of Pharmaceutical ReseaRch, K Sekhri, R Nandha, S Aditya - 2014 - wjpr.net

31. The JAK inhibitor tofacitinib suppresses synovial JAK1-STAT signalling in rheumatoid arthritis, DL Boyle et al,

Annals of the …, 2014 - ard.bmj.com

32. Перспективы фармакотерапии ревматоидного артрита: моноклональные антитела, ЕЛ Насонов, ЛН

Денисов… - Научно-практическая …, 2012 - cyberleninka.ru

33. Thymidine Phosphorylase Regulates the Expression of CXCL10 in Rheumatoid Arthritis Fibroblast‐like

Synoviocytes, Y Toyoda et al, Arthritis & …, 2014 - Wiley Online Library

34. Chemokines and chemokine receptors blockers as new drugs for the treatment of chronic obstructive

pulmonary disease, G Caramori, A Di Stefano, P Casolari… - Current medicinal …, 2013 - ingentaconnect.com

35. Brief Report: Inadequate Description and Discussion of Enrolled Patient Characteristics and Potential Inter–

Study Site Differences in Reports of Randomized …, S Yurdakul, BN Mustafa, I Fresko… - Arthritis & …, 2014 -

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05 IAN 2015

CODRINA ANCUTA