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

NCT03870334 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2023-12-04

Study results available
· View outcomes & findings →

Summary

This is a phase 2 randomized, placebo-controlled, double-blind, parallel-group multicenter induction study.

Conditions

Interventions

DRUG

BT-11 880 mg

Oral once daily tablet

DRUG

Placebo

Oral once daily tablet

Sponsors & Collaborators

  • NImmune Biopharma

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-05
Primary Completion
2022-08-26
Completion
2022-08-26
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03870334 on ClinicalTrials.gov