drugset / Trial / NCT05057273

Safety and Efficacy of Oral BT-11 in Crohn's Disease Patients With Moderate to Severe Disease

NCT05057273 ↗

Phase 2 Withdrawn NImmune Biopharma
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a phase 2, randomized, double-blind, multicenter study to assess the therapeutic efficacy, safety, and mechanisms of omilancor (BT-11) in patients with moderate to severe Crohn's Disease (CD).

Timeline

Start
2021-11
Primary completion
2022-02
Completion
2022-02

Outcome

Outcome not reported

Stopped: “Decision by Landos Biopharma (not related to safety or efficacy)”

Drugs

EvaluationDrugModalityDoseRoute
Subject omilancor Small molecule 880 mg Oral

Indications