About this trial

This is a Phase 2, multicenter, platform study in adult participants with IBD (moderately to severely active Crohn's Disease or Ulcerative Colitis). The primary goal of this study is to assess the safety and efficacy of multiple investigational drugs.

Eligibility criteria

Qualifiers

Diagnosis of Crohn's Disease (CD), as confirmed by endoscopy and histopathology

Moderately to severely active CD as defined by Clinical Disease Activity Index (CDAI) and Simple Endoscopic Score (SES-CD)

Meets drug stabilization requirements

Diagnosis of Ulcerative Colitis (UC), as confirmed by endoscopy and histopathology

Disqualifiers

Diagnosis of indeterminate colitis

Suspected or diagnosed intra-abdominal or perianal abscess at Screening

Previous small bowel resection with combined resected length of > 100 cm or previous colonic resection of > 2 segments

CD isolated to the stomach, duodenum, jejunum, or perianal region, without colonic and/or ileal involvement

Trial design

Treatments tested in this trial

  • MT-501
  • MT-201

Treatment groups

140 Participants
are divided into 3 treatment groups

Locations

66
Canada
Mirador Therapeutics Selected Site Toronto Canada
Georgia
Mirador Therapeutics Selected Site Kutaisi Georgia
Mirador Therapeutics Selected Site Marneuli Georgia
Mirador Therapeutics Selected Site0102, Tbilisi Georgia

Sponsors and collaborators

Mirador Therapeutics, Inc.

Lead sponsor