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El ensayo clínico NCT06819891 (SIBERITE-2) para Moderately to Severely Active Crohns Disease está reclutando. Consulte la vista de tarjeta del Radar de Ensayos Clínicos y las herramientas de descubrimiento de IA para conocer todos los detalles. O haga cualquier pregunta aquí.
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A Study to Assess the Efficacy and Safety of Induction Therapy With Afimkibart (RO7790121) in Participants With Moderately to Severely Active Crohn's Disease (SIBERITE-2) Fase III 425 Doble ciego Controlado con placebo

Reclutando
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El ensayo clínico NCT06819891 (SIBERITE-2) está diseñado para estudiar el tratamiento de Moderately to Severely Active Crohns Disease. Es un estudio intervencionista de Fase III. Su estado actual es: reclutando. El estudio se inició el 12 de mayo de 2025, con el objetivo de reclutar a 425 participantes. Dirigido por Roche, se espera que finalice el 30 de abril de 2033. Los datos se actualizaron por última vez en ClinicalTrials.gov el 16 de marzo de 2026.
Resumen
This Phase III, multicenter, double-blind, placebo-controlled study will evaluate the efficacy and safety of induction therapy with Afimkibart (also known as RO7790121) in participants with moderately to severely active Crohn's disease (CD).
Título oficial

A Phase III, Multicenter, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Induction Therapy With RO7790121 in Patients With Moderately to Severely Active Crohn's Disease

Condiciones médicas
Moderately to Severely Active Crohns Disease
Otros ID del estudio
  • SIBERITE-2
  • GA45332
  • 2024-513054-30-00 (Número CTIS (UE))
Número del NCT
Inicio del estudio (real)
2025-05-12
Última actualización
2026-03-16
Fecha de finalización (estimada)
2033-04-30
Inscripción (prevista)
425
Tipo de estudio
Intervencionista
FASE
Fase III
Estado general
Reclutando
Objetivo principal
Tratamiento
Método de asignación
Aleatorizado
Modelo de intervención
Paralelo
Enmascaramiento
Doble ciego
Brazos / Intervenciones
Grupo de participantesIntervención/Tratamiento
ExperimentalAfimkibart
Participants will receive afimkibart intravenously (IV) followed by afimkibart subcutaneous (SC) injection.
Afimkibart
Afimkibart will be administered as IV infusion. Afimkibart will be administered as SC injection.
Comparador placeboPlacebo
Participants will receive placebo IV followed by afimkibart SC injection.
PLACEBO
Placebo matching IV afimkibart.
Resultado primario
Medida de resultadoDescripción de la medidaPeriodo de tiempo
Percentage of Participants with Clinical Remission per Crohn's Disease Activity Index (CDAI) Score
Percentage of participants achieving a CDAI score of \<150. The index is a weighted sum of scores on eight components: number of liquid or soft stools (stool frequency), abdominal pain, general well-being, number of complications, use of anti-diarrheal medication, presence of an abdominal mass, hematocrit, and percentage deviation from standard body weight. CDAI generally ranges from 0 to roughly 600, with higher values indicating greater activity.
At Week 12
Percentage of Participants with Endoscopic Response
Percentage of participants achieving a decrease in Simple Endoscopic Score for Crohn's Disease (SES-CD) of \>=50% from baseline. The SES-CD is a composite of four features of endoscopic activity (presence and size of ulcers, extent of ulcerated surface, extent of affected and presence and type of narrowings or stenosis) in up to five ileocolonic segments (terminal ileum, right colon, transverse colon, sigmoid and left colon, and rectum). Each feature is scored on a scale from 0 to 3, giving segment subscores of 0 to 12 points and a total SES-CD range of 0-60, with a higher value indicating greater severity.
At Week 12
Resultado secundario
Medida de resultadoDescripción de la medidaPeriodo de tiempo
Percentage of Participants with Symptomatic Remission
Percentage of participants with the daily number of liquid or very soft stools \<=2.8 and the average of daily abdominal pain scores in the past week \<=1, with neither being greater than baseline.
At Week 12
Percentage of Participants with Endoscopic Remission
Percentage of participants with an SES-CD of 0 to 4 with a decrease from baseline \>=2 and no subscore \>1.
At Week 12
Percentage of Participants with Ulcer-free Endoscopy
Percentage of participants with an SES-CD ulcerated surface subscore of 0.
At Week 12
Average of Daily Number of Liquid or Very Soft Stools in the Past Week (SF)
Daily average number of liquid or very soft stools over 7 days.
Baseline through Week 12
Average of Daily Abdominal Pain Scores in the Past Week (APS)
The average daily rating of abdominal pain in the past 7 days. The pain is assessed on a scale of 0-3 with 0 indicating no pain and 3 indicating severe pain.
Baseline through Week 12
Bowel Urgency
Bowel urgency from baseline through week 12 and. Bowel urgency is a single-item self-reported assessment of sudden or immediate need to have a bowel movement in the past 24 hours. The item response is reported on a 4-point Likert scale, from "None" to "Severe."
Baseline to Week 12
Fatigue
Fatigue, as measured by the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F), from baseline to Week 12. FACIT-F is a 13-item self-reported assessment of fatigue. Each item response option indicates the degree to which a given statement describing the level or impact of fatigue applies in the past 7 days. Response options are graded on a 5-point Likert-type scale, from "Not at all" to "Very much."
Baseline to Week 12
Inflammatory Bowel Disease Questionnaire (IBDQ) Score
Change in IBDQ score from baseline to week 12. The IBDQ is a 32-item questionnaire that measures four domains: bowel symptoms (10 questions); systemic symptoms (5 questions); emotional function (12 questions); and social function (5 questions). The total score ranges from 32-224, with a higher score indicating a better quality of life.
Baseline to Week 12
Percentage of Participants with Clinical Remission: Among Biomarker-Defined Subgroups of Participants
Percentage of participants achieving a CDAI score of \<150 at Week 12 in biomarker-defined subgroups. The index is a weighted sum of scores on eight components: number of liquid or soft stools (stool frequency), abdominal pain, general well-being, number of complications, use of anti-diarrheal medication, presence of an abdominal mass, hematocrit, and percentage deviation from standard body weight. CDAI generally ranges from 0 to roughly 600, with higher values indicating greater activity.
At Week 12
Percentage of Participants with Endoscopic Response: Among Biomarker-Defined Subgroups of Participants
Percentage of participants achieving a decrease in SES-CD of \>=50% from baseline. The SES-CD is a composite of four features of endoscopic activity (presence and size of ulcers, extent of ulcerated surface, extent of affected and presence and type of narrowings or stenosis) in up to five ileocolonic segments (terminal ileum, right colon, transverse colon, sigmoid and left colon, and rectum). Each feature is scored on a scale from 0 to 3, giving segment subscores of 0 to 12 points and a total SES-CD range of 0-60, with a higher value indicating greater severity.
At Week 12
Percentage of Participants with Clinical Response
Percentage of participants with a decrease \>=100 in CDAI from baseline.
At Week 12
Percentage of Participants with Symptomatic Response
Percentage of participants with a decrease \>=30% in both SF and APS, with neither being greater than baseline.
At Week 12
Overall Change in CD Symptoms
Overall change in CD symptoms, as measured by the Patient Global Impression of Change (PGIC) from baseline to Weeks 2, 6 and 12. PGIC measures overall change in Crohn's disease symptoms from "Much better" to "Much worse".
Baseline to Weeks 2, 6 and 12
Overall Severity in CD Symptoms
Overall severity in CD symptoms, as measured by the Patient Global Impression of Severity (PGIS) from baseline to Weeks 2, 6 and 12. PGIS measures severity of Crohn's disease symptoms from "None" to "Very severe".
Baseline to Weeks 2, 6 and 12
Change in General Well-being
The average daily rating of general well-being in the past 7 days. Well-being is assessed on a scale of 0-4 with 0 indicating generally well and 4 indicating terrible.
Baseline through Week 12
Incidence and Severity of Adverse Events (AEs)
Incidence and severity of AEs, including serious AEs, AEs leading to treatment discontinuation and AEs of special interest.
Up to 30 Weeks after Baseline
Presence of Draining Fistulas
Fistulas will be assessed for draining or closed status, where closed fistulas will be assessed by the investigator as no longer draining.
Baseline through Week 12
Asistente de participación
Criterios de elegibilidad

Criterios de edad
Niño, Adulto, Adulto mayor
Edad mínima
16 Years
Criterios de sexo
Todos
  • Confirmed diagnosis of CD
  • Moderately to severely active CD
  • Bodyweight >= 40 kilogram (kg)
  • Demonstrated inadequate response, loss of response and/or intolerance to at least one protocol-specified conventional or advanced CD therapy
  • Males and females of childbearing potential must meet protocol criteria for contraception requirements

  • Current diagnosis of ulcerative colitis (UC) or indeterminate colitis, ischemic colitis, infectious colitis, radiation colitis, microscopic colitis
  • Participant with a history of >= 3 bowel resections (> 2 missing segments of the 5 following segments: terminal ilelium, right colon, transverse colon, sigmoid and left colon, and rectum)
  • Diagnosis of short gut or short bowel syndrome
  • Presence of an ileostomy, colostomy or ileoanal pouch
  • Participants with symptomatic bowel strictures, fulminant colitis, or toxic megacolon
  • Presence of abdominal or perianal abscess
  • Presence of rectovaginal, enterovaginal, high output enterocutaneous fistula, enterovesical fistulas or perianal fistulas with >3 openings
  • Participants with symptomatic bowel strictures, fulminant colitis, or toxic megacolon
  • Current diagnosis or suspicion of primary sclerosing cholangitis
  • Pregnancy or breastfeeding, or intention of becoming pregnant during the study
  • Any past or current evidence of cancer of gastrointestinal tract, definite low-grade or high-grade colonic dysplasia
  • History of non-gastrointestinal cancer, with the exception of adequately treated non-metastatic basal cell or squamous cell skin cancer or in situ cervical cancer
  • Evidence of infection with Clostridioides difficile (C. difficile; formerly known as Clostridium difficile), cytomegalovirus (CMV), human immunodeficiency virus (HIV), Hepatitis B (HBV), Hepatitis C (HCV) during screening
  • Has evidence of active tuberculosis (TB), latent TB not successfully treated (per local guidance) or inadequately treated TB
  • Has received protocol-specified prohibited medicines, including known exposure to any type of anti-TL1A therapy
Chugai Pharmaceutical logoChugai Pharmaceutical
Contactos centrales del estudio
Contacto: Reference Study ID Number: GA45332 https://forpatients.roche.com/, 888-662-6728 (U.S. and Canada), [email protected]
162 Centros del estudio en 24 países

Madrid

Fundacion Hospital de Alcorcon, Alcorcón, Madrid, 28922, Spain
Reclutando
Hospital General Universitario Gregorio Maranon, Madrid, 28040, Spain
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Hospital Clinico Univ. Lozano Blesa, Zaragoza, 50009, Spain
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Instituto Medico CER, Quilmes, B1878DVB, Argentina
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CICE 9 de Julio, San Miguel de Tucumán, T4000DPK, Argentina
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Hospital Universitario San Ignacio, Bogotá, 000472, Colombia
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Clínica de la Mujer, Bogotá, 110221, Colombia
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Oncomedica S.A., Montería, 230002, Colombia
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Medicina de Precisión - Celerity, Las Condes, 7560908, Chile
Reclutando
Centro de Investigación Clínica UC-CICUC, Santiago, 8330034, Chile
Reclutando

Arizona

Sun City Clinical Research, Glendale, Arizona, 85304, United States
Reclutando

California

Om Research LLC, Lancaster, California, 93534, United States
Reclutando
Hoag Memorial Hospital Presbyterian;Hoag Center for Research and Education, Newport Beach, California, 92663, United States
Reclutando
Empire Clinical Research, Pomona, California, 91767, United States
Retirado
Stanford Medicine Outpatient Center, Redwood City, California, 94063, United States
Reclutando
Amicis Research Center, Santa Clarita, California, 91355, United States
Reclutando

Colorado

Peak Gastroenterology Associates, Colorado Springs, Colorado, 80907, United States
Reclutando

Florida

J&A Clinical Research, Doral, Florida, 33126, United States
Reclutando
Homestead Associates in Research, Inc., Miami, Florida, 33033, United States
Reclutando
Allied Biomedical Research Institute, Inc, Miami, Florida, 33155, United States
Reclutando
Rejuvaline Medical Research, Miami, Florida, 33155, United States
Reclutando
Miami Beach Clinical Research Center, Miami Beach, Florida, 33141, United States
Reclutando
Eminat Research Group, Miramar, Florida, 33027, United States
Reclutando
Digestive and Liver Center of Florida, Orlando, Florida, 32825, United States
Reclutando
Advanced Medical Research Center, Port Orange, Florida, 32127, United States
Reclutando
Santos Research Center, CORP, Tampa, Florida, 33615, United States
Reclutando

Illinois

The University of Chicago, Chicago, Illinois, 60637, United States
Reclutando

Kentucky

Robley Rex VA Medical Center, Louisville, Kentucky, 40206, United States
Reclutando

Louisiana

Baton Rouge General Medical Center, Baton Rouge, Louisiana, 70809, United States
Reclutando
Louisiana Research Center - GastroIntestinal Associates, Shreveport, Louisiana, 71105, United States
Reclutando

Maryland

Mercy Medical Center, Baltimore, Maryland, 21202, United States
Reclutando
Chevy Chase Clinical Research, Chevy Chase, Maryland, 20815, United States
Reclutando

Massachusetts

University of Massachusetts Memorial Medical Center, North Worcester, Massachusetts, 01655, United States
Reclutando

Michigan

Gastroenterology Associates of Western Michigan, P.L.C., Wyoming, Michigan, 49519, United States
Reclutando

Mississippi

Gastrointestinal Associates Research, Flowood, Mississippi, 39232, United States
Reclutando

New Jersey

Virtua Crohns and Colitis Center, Moorestown, New Jersey, 08057, United States
Reclutando
Robert Wood Johnson University Hospital, New Brunswick, New Jersey, 08901, United States
Reclutando

New York

Ellipsis Research Group, Brooklyn, New York, 11215, United States
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Intercity Gastroenterology, Fresh Meadows, New York, 11366, United States
Reclutando
James J Peters Veterans Affairs Medical Center, The Bronx, New York, 10468, United States
Reclutando
Digestive Disease Medicine of Central New York, Utica, New York, 13502, United States
Reclutando

North Carolina

Charlotte Gastroenterology and Hepatology, P.L.L.C, Charlotte, North Carolina, 28207, United States
Reclutando

Ohio

Clinical Inquest Center, Beavercreek, Ohio, 45431, United States
Reclutando
Cleveland Clinic Foundation, Cleveland, Ohio, 44195, United States
Reclutando

Tennessee

Vanderbilt University Medical Center, Nashville, Tennessee, 37212-1375, United States
Reclutando

Texas

University of Texas Southwestern Medical Center - Multidisciplinary Spine Clinic - James W. Aston Ambulatory Care Center, Dallas, Texas, 75390-8565, United States
Reclutando
GI Alliance - Fort Worth, Fort Worth, Texas, 76104, United States
Reclutando
GI Alliance, Garland, Texas, 75044, United States
Reclutando
Integrity Advanced Therapeutics PLLC, Houston, Texas, 77090, United States
Reclutando
Carta - Clinical Associates In Research Therapeutics Of America;LLC, San Antonio, Texas, 78212, United States
Reclutando
University of Texas Health Center at Tyler, Tyler, Texas, 75708, United States
Reclutando
TDDC GI Alliance research Webster, Webster, Texas, 77598, United States
Reclutando

West Virginia

University Physicians and Surgeons Inc, dba Marshall Health, Huntington, West Virginia, 25701, United States
Reclutando

New South Wales

Macquarie University Hospital, Macquarie Park, New South Wales, 2109, Australia
Reclutando

Queensland

Coral Sea Clinical Research Institute, Mackay, Queensland, 4740, Australia
Retirado

Victoria

Footscray Hospital, Footscray, Victoria, 3011, Australia
Reclutando
Royal Melbourne Hospital, Parkville, Victoria, 3050, Australia
Reclutando
Ordensklinikum Linz Barmherzige Schwestern, Linz, 4010, Austria
Reclutando
Klinikum Wels-Grieskirchen, Wels, 4600, Austria
Reclutando
CHU St Pierre (St Pierre), Brussels, 1000, Belgium
Reclutando
UZ Brussel, Brussels, 1090, Belgium
Reclutando
Cliniques Universitaires St-Luc, Brussels, 1200, Belgium
Reclutando

Rio de Janeiro

Instituto Lobus Unimed Volta Redonda, Volta Redonda, Rio de Janeiro, 27258-000, Brazil
Reclutando

Rio Grande do Sul

Hospital Moinhos de Vento, Porto Alegre, Rio Grande do Sul, 90035-000, Brazil
Reclutando

Sergipe

Newdata Clinical Trials, Aracaju, Sergipe, 49055-000, Brazil
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São Paulo

CECIP - Centro de Estudos Clínicos do Interior Paulista, Jaú, São Paulo, 17210-190, Brazil
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Hospital de Base de Sao Jose do Rio Preto, São José do Rio Preto, São Paulo, 15090-000, Brazil
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Hospital Sírio-Libanês, São Paulo, São Paulo, 01308-050, Brazil
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MC " Sveti Ivan Rilski Chudotvorets- 2010, Plovdiv, 4003, Bulgaria
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Ontario

Barrie GI Associates, Barrie, Ontario, L4M 7G1, Canada
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GNRR Digestive Clinics and Research Center Inc., Brampton, Ontario, L6S 0E2, Canada
Reclutando
London Health Sciences Centre Uni Campus, London, Ontario, N6A 5A5, Canada
Reclutando
LDDI Clinical Trials Inc., London, Ontario, N6K 1M6, Canada
Reclutando
Toronto Immune and Digestive Health Institute, North YORK, Ontario, M6A 3B4, Canada
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Quebec

CIUSSS de l Est de l Ile de Montreal - Hopital Maisonneuve Rosemont, Montreal, Quebec, H1T 2M4, Canada
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Jiangxi

First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, 341000, China
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Yunnan

The First Affilliated Hospital of Kunming Medical University, Kunming, Yunnan, 650032, China
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Zhejiang

Jinhua municipal central hospital, Jinhua, Zhejiang, 321013, China
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Beijing Union Hospital, Beijing, 100730, China
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Sichuan Provincial People's Hospital, Chengdu, 610072, China
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Guangzhou First People's Hospital, Guangzhou, 510180, China
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Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China
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Hainan General Hospital, Haikou, 570311, China
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Huizhou First Hospital, Huizhou, China
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The Second Affiliated Hospital of Nanchang University, Nanchang, 330008, China
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Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China
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Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China
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Shengjing Hospital of China Medical University, Shenyang, 110004, China
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Hebei Medical University - The Second Hospital, Shijiazhuang, 050004, China
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The Second Affiliated Hospital of Soochow University, Suzhou, 215004, China
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The Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, 710004, China
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The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China
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Affiliated Hospital of Jiangsu University, Zhenjiang, 212001, China
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Borzan Polyclinic, Osijek, 31000, Croatia
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Hepato-Gastroenterologie HK, s.r.o., Hradec Králové, 500 12, Czechia
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Fakultni nemocnice Ostrava, Ostrava - Poruba, 708 52, Czechia
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Institutu Klinicke a Experimentaini Mediciny (IKEM);Klinika hepatogastroenterologie, Prague, 140 21, Czechia
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ISCARE a.s., Prague, 170 04, Czechia
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Krajska zdravotni, a.s. ? Masarykova nemocnice v Usti nad Labem, o.z., Ocni oddeleni, Ústí nad Labem, 401 13, Czechia
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CHU Tours - Hôpital Trousseau, Chambray-lès-Tours, 37170, France
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CHU Clermont Ferrand - Hôpital d'Estaing, Clermont-Ferrand, 63000, France
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Hôpital Henri Mondor, Créteil, 94000, France
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CH Dptal Les Oudairies, La Roche-sur-Yon, 85925, France
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CHRU de Lille - Hopital Claude Huriez, Lille, 59037, France
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Hopital Dupuytren, Limoges, 87042, France
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Hopital Saint-Eloi, Montpellier, 34295, France
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Institut des MICI, Clinique Ambroise Paré, Neuilly-sur-Seine, 92200, France
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Hôpital Saint-Louis, Paris, 75475, France
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Centre Hospitalier Lyon Sud, Pierre-Bénite, 69495, France
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Hôpital de Brabois Adultes, Vandœuvre-lès-Nancy, 54511, France
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Universitätsklinikum Heidelberg, Heidelberg, 69120, Germany
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Klinikum Ernst von Bergmann, Potsdam, 14467, Germany
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Észak-Pesti Centrumkórház-Honvédkórház, Budapest, 1062, Hungary
Reclutando
Geomedical Orvosi Kft, Budapest, 1066, Hungary
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Semmelweis Egyetem, Budapest, 1082, Hungary
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Endomedix Kft., Budapest, 1139, Hungary
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Vas-Oxy Egeszsegugyi Kft, Szombathely, 9700, Hungary
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Gujarat

Shree Giriraj Multispeciality Hospital, Rajkot, Gujarat, 360005, India
Reclutando
Surat Institute of Digestive Sciences Hospitals, Surat, Gujarat, 395002, India
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Gujarat Gastro and Vascular Hospital, Surat, Gujarat, 395009, India
Reclutando

Kerala

Amrita Institute of Medical Sciences, Kochi, Kerala, 682041, India
Reclutando

Maharashtra

MIDAS Multispeciality Hospital, Nagpur (urban), Maharashtra, 440018, India
Reclutando

National Capital Territory of Delhi

All India Institute Of Medical Sciences (AIIMS), New Delhi, National Capital Territory of Delhi, 110029, India
Reclutando

Rajasthan

SR Kalla Memorial Gastro & General Hospital, Jaipur, Rajasthan, 302006, India
Reclutando

Telangana

AIG Hospitals, Gachibowli, Telangana, 500032, India
Reclutando
Yashoda Hospitals, Secunderabad, Telangana, 500003, India
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Shaare Zedek Medical Center, Jerusalem, 9103102, Israel
Reclutando

Basilicate

Ospedale Madonna delle Grazie, Matera, Basilicate, 75100, Italy
Reclutando

Emilia-Romagna

Azienda Ospedaliero Universitaria Di Bologna - Policlinico S Orsola Malpighi-Via Massarenti, Bologna, Emilia-Romagna, 40138, Italy
Reclutando

Lazio

Policlinico Universitario Campus Biomedico Di Roma, Rome, Lazio, 00128, Italy
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Policlinico Universitario Agostino Gemelli, Rome, Lazio, 00168, Italy
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Lombardy

Asst Degli Spedali Civili Di Brescia, Brescia, Lombardy, 25123, Italy
Reclutando
IRCCS Ospedale San Raffaele, Milan, Lombardy, 20132, Italy
Reclutando
I.R.C.C.S Policlinico San Donato, San Donato Milanese (MI), Lombardy, 20097, Italy
Reclutando

Veneto

IRCCS Ospedale Sacro Cuore Don Calabria, Negrar, Veneto, 37024, Italy
Reclutando
Gastromed Kralisz, Romatowski, Stachurska sp.j., Bia?ystok, 15-322, Poland
Reclutando
Medical Center Kermed, Bydgoszcz, 85-231, Poland
Reclutando
Szpital Miejski sw. Jana Paw?a II w Elblagu, Elblag, 82-300, Poland
Reclutando
Osrodek Badan Klinicznych Bd Research, I?awa, 14-200, Poland
Reclutando
MZ Badania Slowik Zymla Sp.j., Knurów, 44-190, Poland
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Centrum Medyczne Promed, Krakow, 31-513, Poland
Reclutando
Amicare Sp. z o.o. S.K., Lodz, 91-495, Poland
Reclutando
Medrise sp z o.o, Lublin, 20-582, Poland
Reclutando
Clinical Research Center Sp. z o.o. MEDIC-R Spó?ka Komandytowa, Poznan, 61-731, Poland
Reclutando
EMC Instytut Medyczny SA, Późna, 60-309, Poland
Reclutando
Gabinety Lekarskie Rivermed, Późna, 61-441, Poland
Reclutando
Endoskopia Sp. z o.o., Sopot, 81-756, Poland
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Sonomed Sp. z o.o., Szczecin, 71-685, Poland
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Centrum Zdrowia-MDM, Warsaw, 00-189, Poland
Reclutando
Medon Clinical Research sp. z o.o, Warsaw, 02-679, Poland
Reclutando
Vivamed Spolka Z Ograniczona Odpowiedzialnoscia, Warsaw, 03-580, Poland
Reclutando
PlanetMed sp. z o.o., Wroc?aw, 52-210, Poland
Reclutando
Hospital de Braga, Braga, 4710-243, Portugal
Reclutando
Hospital de Santa Maria, Lisbon, 1649-035, Portugal
Reclutando
Hospital de Sao Joao, Porto, 4202-451, Portugal
Reclutando
Centro Hospitalar de Entre Douro e Vouga - H. São Sebastião, Santa Maria da Feira, 4520-211, Portugal
Reclutando
Hospital Sao Teotonio, Viseu, 3504-509, Portugal
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ABAWI spol. s r.o., Bratislava, 821 07, Slovakia
Reclutando
KM Management spol. s r.o., Nitra, 949 01, Slovakia
Reclutando
Fairfield General Hospital, Bury, BL9 7TD, United Kingdom
Reclutando
Bronglais General Hospital, Llanrhystud, SY23 1ER, United Kingdom
Reclutando
Royal London Hospital, London, E1 1FR, United Kingdom
Reclutando