Tests BRS201 in adults with ulcerative colitis that has not responded to treatment

Trial details

Who runs it

Brigham and Women's Hospital

Trial code

NCT06420492

Record updated

20 October 2025

Original description

This study is a clinical trial being done to investigate the efficacy of drug BRS201 as a treatment in patients with acute ulcerative colitis. Patients who qualify are adults who have not responded to treatments for their severe ulcerative colitis. Participation in this study will take 12 weeks long and the study is structured as an open-label pilot study in which participants will take the study drug for 4 weeks in the form of an oral medication. Participation may also involve receiving an IV dose of the medication. The study will require participants to attend 8 study visits, all of which will be conducted at a study site. Participation will involve taking an oral medication twice daily, tracking the medication in a log, and getting blood drawn and giving a stool and urine sample for a few lab tests throughout the study. Participants may also undergo a flexible sigmoidoscopy at the beginning and end of the study.Read full original descriptionShow less

Study of Novel Therapeutics for Acute Remedy of Colitis

This study is a clinical trial being done to investigate the efficacy of drug BRS201 as a treatment in patients with acute ulcerative colitis. Patients who qualify are adults who have not responded to treatments for their severe ulcerative colitis. Participation in this study will take 12 weeks long and the study is structured as an open-label pilot study in which participants will take the study drug for 4 weeks in the form of an oral medication. Participation may also involve receiving an IV dose of the medication. The study will require participants to attend 8 study visits, all of which will be conducted at a study site. Participation will involve taking an oral medication twice daily, tracking the medication in a log, and getting blood drawn and giving a stool and urine sample for a few lab tests throughout the study. Participants may also undergo a flexible sigmoidoscopy at the beginning and end of the study.

Inclusion: Severe outpatient or hospitalized for an acute UC flare; Ability to give consent; Patients with a confirmed diagnosis of UC for > 3 months; History of ≥ 15 cm of colonic involvement as confirmed by colonoscopy; Patients with primary sclerosing cholangitis are eligible to enroll; Patients will have failed 5 days of oral prednisone 30 mg or greater for 5 days and still having a SCCAI of > 6; Patients who are taking 20mg or less of oral prednisone and plan to stay at that dose during their participation in the study; Accepted medications:; Anti-TNF agents are permissible if the patient has been taking them for at least 10 weeks and anticipates to maintain a steady for the duration of the study; Rinvoq (Upadacitinib) is permissible if the subject has been taking this medication for at least 4 weeks and anticipates to maintain a steady dose for the duration of the study; Xeljanz (Tofacitinib) is permissible if the subject has been taking this medication for at least 4 weeks and anticipates to maintain a steady dose for the duration of the study; Other biologics are permissible if the subject has been taking the medication for at least 10 weeks and anticipates to maintain a steady dose for the duration of the study.

Exclusion: Infectious Colitis or drug induced colitis; Prohibited medications:; Rinvoq (Upadacitinib): Subjects will be excluded from this study if their last dose of this medication was administered within 4 weeks. If subjects have stopped taking this medication and their last dose was administered more than 4 weeks prior to enrollment, they will be eligible for participation; Xeljanz (Tofacitinib): Subjects will be excluded from this study if their last dose of this medication was administered within 4 weeks. If subjects have stopped taking this medication and their last dose was administered more than 4 weeks prior to enrollment, they will be eligible for participation; Other Medications: Subjects will be excluded from this study if they stopped taking any other medications for ulcerative colitis within 8 weeks. If subjects have stopped taking the medication and their last dose was more than 8 weeks prior to enrollment, they will be eligible for participation; History of uncontrolled hypertension with systolic BP > 140 and systolic BP > 90; Crohn's Disease or Indeterminate colitis; Decompensated liver disease; Patients who have a confirmed malignancy or cancer within 5 years; Other comorbidities including: Diabetes mellitus, systemic lupus; Chronic kidney disease as defined by GFR <55mL/min; Impaired hepatic function (transaminases elevated > 2.5 x ULN) unless due to PSC; Patients with a history or risk of cardiovascular conditions, including arrhythmia, long QT syndrome, congestive heart failure, stroke, or coronary artery disease; Evidence of C. difficile (Negative test result within 1 month is acceptable); Patients who are pregnant or breastfeeding; Congenital or acquired immunodeficiencies; Participation in a therapeutic clinical trial in the preceding 30 days or simultaneously during this trial.

ClinicalTrials.gov NCT06420492