רדאר קליני AI | ||
|---|---|---|
הניסוי הקליני NCT06819891 (SIBERITE-2) עבור Moderately to Severely Active Crohns Disease הוא מגייס. לכל הפרטים, עיינו בתצוגת הכרטיסים של רדאר ניסויים קליניים ובכלי הגילוי של AI. אפשר גם לשאול כל דבר כאן. | ||
מחקר אחד תואם לקריטריוני המסנן
תצוגת כרטיסים
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) שלב III 425 סמיות כפולה מבוקר פלסבו
פרטי הניסויים הקליניים זמינים בעיקר באנגלית. רדאר קליני AI יכול לעזור! לחץ על 'הסבר את המחקר' כדי לצפות ולשוחח על מידע מהמחקר בשפה המועדפת עליך.
ניסוי קליני NCT06819891 (SIBERITE-2) מתקיים כדי לבדוק את טיפול עבור Moderately to Severely Active Crohns Disease. זהו מחקר שלב III מסוג התערבותי שנמצא כעת במצב מגייס. המחקר התחיל ב-12 במאי 2025 ומתוכנן לכלול 425 משתתפים. המחקר מנוהל על ידי רוש וצפוי להסתיים ב-30 באפריל 2033. מידע זה עודכן לאחרונה באתר ClinicalTrials.gov ב-16 במרץ 2026.
סיכום קצר
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).
כותרת רשמית
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
מצבים רפואיים
Moderately to Severely Active Crohns Diseaseמזהי מחקר נוספים
- SIBERITE-2
- GA45332
- 2024-513054-30-00 (מספר מחקר של האיחוד האירופי (CTIS))
מספר NCT
תחילת המחקר (בפועל)
2025-05-12
עדכון אחרון שפורסם
2026-03-16
סיום המחקר (מוערך)
2033-04-30
משתתפים (מתוכנן)
425
סוג המחקר
התערבותי
שלב
שלב III
סטטוס
מגייס
מטרה ראשית
טיפול
הקצאת טיפול
אקראי
דגם מתערב
קבוצות מקבילות
עיוורון
כפול
זרועות / התערבויות
| קבוצת משתתפים/זרוע | התערבות/טיפול |
|---|---|
ניסיAfimkibart 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. |
פלצבו להשוואהPlacebo Participants will receive placebo IV followed by afimkibart SC injection. | פלצבו Placebo matching IV afimkibart. |
מדדי תוצאה ראשיים
מדדי תוצאה משניים
| מדד תוצאה | תיאור המדידה | טווח זמן |
|---|---|---|
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 |
| מדד תוצאה | תיאור המדידה | טווח זמן |
|---|---|---|
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 |
עוזר השתתפות
קריטריוני זכאות
גילאים מוערכים למחקר
ילד, מבוגר, גיל שלישי
גיל מינימלי למחקר
16 Years
מגדרים מוערכים למחקר
הכל
- 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
איש קשר מרכזי למחקר
איש קשר: Reference Study ID Number: GA45332 https://forpatients.roche.com/, 888-662-6728 (U.S. and Canada), [email protected]
162 מיקומי המחקר ב-24 מדינות
Shaare Zedek Medical Center, Jerusalem, 9103102, Israel
מגייס
Arizona
Sun City Clinical Research, Glendale, Arizona, 85304, United States
מגייס
California
Om Research LLC, Lancaster, California, 93534, United States
מגייס
Hoag Memorial Hospital Presbyterian;Hoag Center for Research and Education, Newport Beach, California, 92663, United States
מגייס
Empire Clinical Research, Pomona, California, 91767, United States
נסוג
Stanford Medicine Outpatient Center, Redwood City, California, 94063, United States
מגייס
Amicis Research Center, Santa Clarita, California, 91355, United States
מגייס
Colorado
Peak Gastroenterology Associates, Colorado Springs, Colorado, 80907, United States
מגייס
Florida
J&A Clinical Research, Doral, Florida, 33126, United States
מגייס
Homestead Associates in Research, Inc., Miami, Florida, 33033, United States
מגייס
Allied Biomedical Research Institute, Inc, Miami, Florida, 33155, United States
מגייס
Rejuvaline Medical Research, Miami, Florida, 33155, United States
מגייס
Miami Beach Clinical Research Center, Miami Beach, Florida, 33141, United States
מגייס
Eminat Research Group, Miramar, Florida, 33027, United States
מגייס
Digestive and Liver Center of Florida, Orlando, Florida, 32825, United States
מגייס
Advanced Medical Research Center, Port Orange, Florida, 32127, United States
מגייס
Santos Research Center, CORP, Tampa, Florida, 33615, United States
מגייס
Illinois
The University of Chicago, Chicago, Illinois, 60637, United States
מגייס
Kentucky
Robley Rex VA Medical Center, Louisville, Kentucky, 40206, United States
מגייס
Louisiana
Baton Rouge General Medical Center, Baton Rouge, Louisiana, 70809, United States
מגייס
Louisiana Research Center - GastroIntestinal Associates, Shreveport, Louisiana, 71105, United States
מגייס
Maryland
Mercy Medical Center, Baltimore, Maryland, 21202, United States
מגייס
Chevy Chase Clinical Research, Chevy Chase, Maryland, 20815, United States
מגייס
Massachusetts
University of Massachusetts Memorial Medical Center, North Worcester, Massachusetts, 01655, United States
מגייס
Michigan
Gastroenterology Associates of Western Michigan, P.L.C., Wyoming, Michigan, 49519, United States
מגייס
Mississippi
Gastrointestinal Associates Research, Flowood, Mississippi, 39232, United States
מגייס
New Jersey
Virtua Crohns and Colitis Center, Moorestown, New Jersey, 08057, United States
מגייס
Robert Wood Johnson University Hospital, New Brunswick, New Jersey, 08901, United States
מגייס
New York
Ellipsis Research Group, Brooklyn, New York, 11215, United States
מגייס
Intercity Gastroenterology, Fresh Meadows, New York, 11366, United States
מגייס
James J Peters Veterans Affairs Medical Center, The Bronx, New York, 10468, United States
מגייס
Digestive Disease Medicine of Central New York, Utica, New York, 13502, United States
מגייס
North Carolina
Charlotte Gastroenterology and Hepatology, P.L.L.C, Charlotte, North Carolina, 28207, United States
מגייס
Ohio
Clinical Inquest Center, Beavercreek, Ohio, 45431, United States
מגייס
Cleveland Clinic Foundation, Cleveland, Ohio, 44195, United States
מגייס
Tennessee
Vanderbilt University Medical Center, Nashville, Tennessee, 37212-1375, United States
מגייס
Texas
University of Texas Southwestern Medical Center - Multidisciplinary Spine Clinic - James W. Aston Ambulatory Care Center, Dallas, Texas, 75390-8565, United States
מגייס
GI Alliance - Fort Worth, Fort Worth, Texas, 76104, United States
מגייס
GI Alliance, Garland, Texas, 75044, United States
מגייס
Integrity Advanced Therapeutics PLLC, Houston, Texas, 77090, United States
מגייס
Carta - Clinical Associates In Research Therapeutics Of America;LLC, San Antonio, Texas, 78212, United States
מגייס
University of Texas Health Center at Tyler, Tyler, Texas, 75708, United States
מגייס
TDDC GI Alliance research Webster, Webster, Texas, 77598, United States
מגייס
West Virginia
University Physicians and Surgeons Inc, dba Marshall Health, Huntington, West Virginia, 25701, United States
מגייס
Instituto Medico CER, Quilmes, B1878DVB, Argentina
מגייס
CICE 9 de Julio, San Miguel de Tucumán, T4000DPK, Argentina
מגייס
New South Wales
Macquarie University Hospital, Macquarie Park, New South Wales, 2109, Australia
מגייס
Queensland
Coral Sea Clinical Research Institute, Mackay, Queensland, 4740, Australia
נסוג
Victoria
Footscray Hospital, Footscray, Victoria, 3011, Australia
מגייס
Royal Melbourne Hospital, Parkville, Victoria, 3050, Australia
מגייס
Ordensklinikum Linz Barmherzige Schwestern, Linz, 4010, Austria
מגייס
Klinikum Wels-Grieskirchen, Wels, 4600, Austria
מגייס
CHU St Pierre (St Pierre), Brussels, 1000, Belgium
מגייס
UZ Brussel, Brussels, 1090, Belgium
מגייס
Cliniques Universitaires St-Luc, Brussels, 1200, Belgium
מגייס
Rio de Janeiro
Instituto Lobus Unimed Volta Redonda, Volta Redonda, Rio de Janeiro, 27258-000, Brazil
מגייס
Rio Grande do Sul
Hospital Moinhos de Vento, Porto Alegre, Rio Grande do Sul, 90035-000, Brazil
מגייס
Sergipe
Newdata Clinical Trials, Aracaju, Sergipe, 49055-000, Brazil
מגייס
São Paulo
CECIP - Centro de Estudos Clínicos do Interior Paulista, Jaú, São Paulo, 17210-190, Brazil
מגייס
Hospital de Base de Sao Jose do Rio Preto, São José do Rio Preto, São Paulo, 15090-000, Brazil
מגייס
Hospital Sírio-Libanês, São Paulo, São Paulo, 01308-050, Brazil
מגייס
MC " Sveti Ivan Rilski Chudotvorets- 2010, Plovdiv, 4003, Bulgaria
מגייס
Ontario
Barrie GI Associates, Barrie, Ontario, L4M 7G1, Canada
מגייס
GNRR Digestive Clinics and Research Center Inc., Brampton, Ontario, L6S 0E2, Canada
מגייס
London Health Sciences Centre Uni Campus, London, Ontario, N6A 5A5, Canada
מגייס
LDDI Clinical Trials Inc., London, Ontario, N6K 1M6, Canada
מגייס
Toronto Immune and Digestive Health Institute, North YORK, Ontario, M6A 3B4, Canada
מגייס
Quebec
CIUSSS de l Est de l Ile de Montreal - Hopital Maisonneuve Rosemont, Montreal, Quebec, H1T 2M4, Canada
מגייס
Medicina de Precisión - Celerity, Las Condes, 7560908, Chile
מגייס
Centro de Investigación Clínica UC-CICUC, Santiago, 8330034, Chile
מגייס
Jiangxi
First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, 341000, China
מגייס
Yunnan
The First Affilliated Hospital of Kunming Medical University, Kunming, Yunnan, 650032, China
מגייס
Zhejiang
Jinhua municipal central hospital, Jinhua, Zhejiang, 321013, China
מגייס
Beijing Union Hospital, Beijing, 100730, China
מגייס
Sichuan Provincial People's Hospital, Chengdu, 610072, China
מגייס
Guangzhou First People's Hospital, Guangzhou, 510180, China
מגייס
Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China
מגייס
Hainan General Hospital, Haikou, 570311, China
מגייס
Huizhou First Hospital, Huizhou, China
מגייס
The Second Affiliated Hospital of Nanchang University, Nanchang, 330008, China
מגייס
Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China
מגייס
Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China
מגייס
Shengjing Hospital of China Medical University, Shenyang, 110004, China
מגייס
Hebei Medical University - The Second Hospital, Shijiazhuang, 050004, China
מגייס
The Second Affiliated Hospital of Soochow University, Suzhou, 215004, China
מגייס
The Second Affiliated Hospital of Xi'an Jiao Tong University, Xi'an, 710004, China
מגייס
The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China
מגייס
Affiliated Hospital of Jiangsu University, Zhenjiang, 212001, China
מגייס
Hospital Universitario San Ignacio, Bogotá, 000472, Colombia
מגייס
Clínica de la Mujer, Bogotá, 110221, Colombia
מגייס
Oncomedica S.A., Montería, 230002, Colombia
מגייס
Borzan Polyclinic, Osijek, 31000, Croatia
מגייס
Hepato-Gastroenterologie HK, s.r.o., Hradec Králové, 500 12, Czechia
מגייס
Fakultni nemocnice Ostrava, Ostrava - Poruba, 708 52, Czechia
מגייס
Institutu Klinicke a Experimentaini Mediciny (IKEM);Klinika hepatogastroenterologie, Prague, 140 21, Czechia
מגייס
ISCARE a.s., Prague, 170 04, Czechia
מגייס
Krajska zdravotni, a.s. ? Masarykova nemocnice v Usti nad Labem, o.z., Ocni oddeleni, Ústí nad Labem, 401 13, Czechia
מגייס
CHU Tours - Hôpital Trousseau, Chambray-lès-Tours, 37170, France
מגייס
CHU Clermont Ferrand - Hôpital d'Estaing, Clermont-Ferrand, 63000, France
מגייס
Hôpital Henri Mondor, Créteil, 94000, France
מגייס
CH Dptal Les Oudairies, La Roche-sur-Yon, 85925, France
מגייס
CHRU de Lille - Hopital Claude Huriez, Lille, 59037, France
מגייס
Hopital Dupuytren, Limoges, 87042, France
מגייס
Hopital Saint-Eloi, Montpellier, 34295, France
מגייס
Institut des MICI, Clinique Ambroise Paré, Neuilly-sur-Seine, 92200, France
מגייס
Hôpital Saint-Louis, Paris, 75475, France
מגייס
Centre Hospitalier Lyon Sud, Pierre-Bénite, 69495, France
מגייס
Hôpital de Brabois Adultes, Vandœuvre-lès-Nancy, 54511, France
מגייס
Universitätsklinikum Heidelberg, Heidelberg, 69120, Germany
מגייס
Klinikum Ernst von Bergmann, Potsdam, 14467, Germany
מגייס
Észak-Pesti Centrumkórház-Honvédkórház, Budapest, 1062, Hungary
מגייס
Geomedical Orvosi Kft, Budapest, 1066, Hungary
מגייס
Semmelweis Egyetem, Budapest, 1082, Hungary
מגייס
Endomedix Kft., Budapest, 1139, Hungary
מגייס
Vas-Oxy Egeszsegugyi Kft, Szombathely, 9700, Hungary
מגייס
Gujarat
Shree Giriraj Multispeciality Hospital, Rajkot, Gujarat, 360005, India
מגייס
Surat Institute of Digestive Sciences Hospitals, Surat, Gujarat, 395002, India
מגייס
Gujarat Gastro and Vascular Hospital, Surat, Gujarat, 395009, India
מגייס
Kerala
Amrita Institute of Medical Sciences, Kochi, Kerala, 682041, India
מגייס
Maharashtra
MIDAS Multispeciality Hospital, Nagpur (urban), Maharashtra, 440018, India
מגייס
National Capital Territory of Delhi
All India Institute Of Medical Sciences (AIIMS), New Delhi, National Capital Territory of Delhi, 110029, India
מגייס
Rajasthan
SR Kalla Memorial Gastro & General Hospital, Jaipur, Rajasthan, 302006, India
מגייס
Telangana
AIG Hospitals, Gachibowli, Telangana, 500032, India
מגייס
Yashoda Hospitals, Secunderabad, Telangana, 500003, India
מגייס
Basilicate
Ospedale Madonna delle Grazie, Matera, Basilicate, 75100, Italy
מגייס
Emilia-Romagna
Azienda Ospedaliero Universitaria Di Bologna - Policlinico S Orsola Malpighi-Via Massarenti, Bologna, Emilia-Romagna, 40138, Italy
מגייס
Lazio
Policlinico Universitario Campus Biomedico Di Roma, Rome, Lazio, 00128, Italy
מגייס
Policlinico Universitario Agostino Gemelli, Rome, Lazio, 00168, Italy
מגייס
Lombardy
Asst Degli Spedali Civili Di Brescia, Brescia, Lombardy, 25123, Italy
מגייס
IRCCS Ospedale San Raffaele, Milan, Lombardy, 20132, Italy
מגייס
I.R.C.C.S Policlinico San Donato, San Donato Milanese (MI), Lombardy, 20097, Italy
מגייס
Veneto
IRCCS Ospedale Sacro Cuore Don Calabria, Negrar, Veneto, 37024, Italy
מגייס
Gastromed Kralisz, Romatowski, Stachurska sp.j., Bia?ystok, 15-322, Poland
מגייס
Medical Center Kermed, Bydgoszcz, 85-231, Poland
מגייס
Szpital Miejski sw. Jana Paw?a II w Elblagu, Elblag, 82-300, Poland
מגייס
Osrodek Badan Klinicznych Bd Research, I?awa, 14-200, Poland
מגייס
MZ Badania Slowik Zymla Sp.j., Knurów, 44-190, Poland
מגייס
Centrum Medyczne Promed, Krakow, 31-513, Poland
מגייס
Amicare Sp. z o.o. S.K., Lodz, 91-495, Poland
מגייס
Medrise sp z o.o, Lublin, 20-582, Poland
מגייס
Clinical Research Center Sp. z o.o. MEDIC-R Spó?ka Komandytowa, Poznan, 61-731, Poland
מגייס
EMC Instytut Medyczny SA, Późna, 60-309, Poland
מגייס
Gabinety Lekarskie Rivermed, Późna, 61-441, Poland
מגייס
Endoskopia Sp. z o.o., Sopot, 81-756, Poland
מגייס
Sonomed Sp. z o.o., Szczecin, 71-685, Poland
מגייס
Centrum Zdrowia-MDM, Warsaw, 00-189, Poland
מגייס
Medon Clinical Research sp. z o.o, Warsaw, 02-679, Poland
מגייס
Vivamed Spolka Z Ograniczona Odpowiedzialnoscia, Warsaw, 03-580, Poland
מגייס
PlanetMed sp. z o.o., Wroc?aw, 52-210, Poland
מגייס
Hospital de Braga, Braga, 4710-243, Portugal
מגייס
Hospital de Santa Maria, Lisbon, 1649-035, Portugal
מגייס
Hospital de Sao Joao, Porto, 4202-451, Portugal
מגייס
Centro Hospitalar de Entre Douro e Vouga - H. São Sebastião, Santa Maria da Feira, 4520-211, Portugal
מגייס
Hospital Sao Teotonio, Viseu, 3504-509, Portugal
מגייס
ABAWI spol. s r.o., Bratislava, 821 07, Slovakia
מגייס
KM Management spol. s r.o., Nitra, 949 01, Slovakia
מגייס
Madrid
Fundacion Hospital de Alcorcon, Alcorcón, Madrid, 28922, Spain
מגייס
Hospital General Universitario Gregorio Maranon, Madrid, 28040, Spain
מגייס
Hospital Clinico Univ. Lozano Blesa, Zaragoza, 50009, Spain
מגייס
Fairfield General Hospital, Bury, BL9 7TD, United Kingdom
מגייס
Bronglais General Hospital, Llanrhystud, SY23 1ER, United Kingdom
מגייס
Royal London Hospital, London, E1 1FR, United Kingdom
מגייס