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Treatment of UC With Novel Therapeutics

Treatment of UC With Novel Therapeutics

Recruiting
18-75 years
All
Phase 2

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Overview

This study is a clinical trial being done to investigate the efficacy of drug BRS201 as a treatment in patients with active mild ulcerative colitis. Participation in this study will take 12 weeks long and the study is structured as a crossover study in which participants will take the study drug for 4 weeks and a placebo drug for 4 weeks in a randomized order 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 7 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.

Eligibility

Inclusion Criteria:

  • 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
  • Disease activity based on calprotectin > 200
  • Allowed medications: mesalamine and sulfasalazine
  • Patients with primary sclerosing cholangitis are eligible to enroll

Exclusion Criteria:

  • History of uncontrolled hypertension with systolic BP > 140 and systolic BP > 90
  • Chronic kidney disease as defined by GFR <55mL/min
  • Impaired hepatic function (transaminases elevated > 2.5 x ULN) unless due to PSC
  • Evidence of C. difficile (Negative test result within 1 month is acceptable)
  • Infectious Colitis or drug induced colitis
  • Crohn's Disease or Indeterminate colitis
  • Decompensated liver disease
  • Patients who are pregnant or breastfeeding
  • Use of rectal therapies
  • Patients who have a confirmed malignancy or cancer within 5 years
  • Congenital or acquired immunodeficiencies
  • Other comorbidities including: Diabetes mellitus, systemic lupus
  • High likelihood of colectomy in the next 2 months
  • Participation in a therapeutic clinical trial in the preceding 30 days or simultaneously during this trial
  • Patients with a history or risk of cardiovascular conditions, including arrhythmia, long QT syndrome, congestive heart failure, stroke, or coronary artery disease
  • Prohibited medications: Vitamin C, prednisone, immune modulators (including but not limited to azathioprine, 6-mercaptopurine, mycophenolate mofetil, tacrolimus, cyclosporine, thalidomide, interleukin-10, interleukin-11, and Omvoh or mirikizumab-mrkz) and biologics within the past six weeks including anti-TNF agents within the past six weeks, vedolizumab within the past six weeks, ustekinumab Risankizumab), a JAKi (tofacitinib or upadacitinib), or Velsipity (etrasimod) within the past 6 weeks. (The aim is to treat people who are having disease activity and just on mesalamine.)

Study details
    Ulcerative Colitis Mild
    Ulcerative Colitis

NCT06420375

Brigham and Women's Hospital

16 June 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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