Last updated 17 days ago
A Study to Investigate Efficacy and Safety of SAR441566 in Patients With Crohn's Disease.
260 patients around the world
Available in United States, Argentina
Sanofi
1Research sites
260Patients around the world
This study is for people with
Crohn's disease
Requirements for the patient
To 75 Years
All Gender
Medical requirements
- Male or female participants aged 18 to 75 years at the time of signing the ICF.Confirmed diagnosis of CD for at least 3 months prior to Baseline.Confirmed diagnosis of moderate to severe CD as assessed by:Crohn's Disease Activity Index (CDAI) score and the Simple Endoscopic Score for Crohn's disease (SES-CD) on an endoscopy confirmed by a central reader.Stool frequency (SF), abdominal pain (AP) score.History of prior exposure to standard treatment (5-ASA, steroids, immunomodulators or antibiotics) or advanced therapies (biologics or small molecules), but having inadequate response to, loss of response to or intolerance to at least one of these therapies.On stable doses of standard treatments prior to screening (Oral 5-ASA compounds, Oral corticosteroids, AZA, 6-MP, or MTX).Contraceptive use by men and women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.Women participants should not be pregnant or breastfeeding.
- Participants with active UC, indeterminate colitis or short bowel syndrome.Participants with CD isolated to the stomach, duodenum, jejunum, or peri anal region, without colonic or ileal involvement.Participants with following ongoing known complications of CD: fistula, abscess, symptomatic stricture/stenosis, fulminant colitis, toxic megacolon, recent bowel resection within 3 months of screening or history of > 3 bowel resections.Participants with stool sample positive for infectious pathogens.Participants with active tuberculosis (TB) or a history of incompletely treated active or latent TB per local guidelines.Participants with Positive Hepatitis B surface antigen (HBsAg) or positive Hepatitis B core antibody (HBcAb); and/or positive Hepatitis C antibody (HCV) at the Screening Visit.Participants with any other active, chronic or recurrent infection, including recurrent or disseminated herpes zoster or disseminated herpes simplex.Participants with a known history of Human Immunodeficiency Virus (HIV) infection or positive HIV-1 or HIV-2 serology at screening.Participants presenting with active malignancies, lymphoproliferative disease, or recurrence of either, within the 5 years before screening.Participants with adenomatous colonic polyps or colonic mucosal dysplasia (low- or high grade) not excised or incompletely excised.Infection(s) requiring treatment with IV anti infectives within 30 days or oral/intramuscular anti-infectives within 14 days prior to the screening visit.Participants requiring or receiving any parental nutrition and/or exclusive enteral nutrition.Participants who received cyclosporine, tacrolimus, mycophenolate mofetil, or thalidomide within 30 days prior to screening.Participants who received fecal microbial transplantation within 30 days prior to screening.Participants who have ever been exposed to natalizumab (Tysabri®) or oral carotegrast methyl (Carogra®).Participants who received IV corticosteroids within 14 days prior to screening or during screening period.Participants who received therapeutic enema or suppository, other than required for colonoscopy within 14 days prior to screening or during screening.Screening laboratory and other analyses show abnormal results.
Sites
Kynet Investigación Clínica
Recruiting
StudySPECIFI-CD
SponsorSanofi
Study typeInterventional
Conditions
Crohn's disease
Requirements
To 75 YearsAll Gender
Unique study IDclinicaltrials.gov
NCT06637631
