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Completed Phase 2 Interventional Results available

A Study Assessing the Efficacy and Safety of CBP-307 in Subjects With Moderate to Severe Ulcerative Colitis (UC)

ClinicalTrials.gov ID: NCT04700449

Public ClinicalTrials.gov record NCT04700449. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 31, 2026, 3:01 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase II Clinical Trial to Evaluate the Efficacy and Safety of CBP-307 in Subjects With Moderate to Severe Ulcerative Colitis (UC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will evaluate the efficacy and safety of CBP-307 in subjects with moderate to severe ulcerative colitis (UC).

Study identification

NCT ID
NCT04700449
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Connect Biopharm LLC
Industry
Enrollment
145 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 27, 2019 (Actual)
Primary completion
Feb 23, 2022 (Actual)
Completion
Nov 10, 2022 (Actual)
Last update posted
May 6, 2024

2019 – 2022

United States locations

U.S. sites
14
U.S. states
7
U.S. cities
12
Facility City State ZIP Site status
Connect Investigative Site 2316 Phoenix Arizona 85018 —
Connect Investigative Site 2308 Mission Hills California 91345 —
Connect Investigative Site 2314 Hialeah Florida 33016 —
Connect Investigative Site 2309 Homestead Florida 33032 —
Connect Investigative Site 2320 Kissimmee Florida 34741 —
Connect Investigative Site 2318 Miami Florida 33126 —
Connect Investigative Site 2302 Orlando Florida 32803 —
Connect Investigative Site 2304 Orlando Florida 32810 —
Connect Investigative Site 2306 Orlando Florida 32819 —
Connect Investigative Site 2307 Atlanta Georgia 30309 —
Connect Investigative Site 2315 Cincinnati Ohio 45219 —
Connect Investigative Site 2321 Oklahoma City Oklahoma 73102 —
Connect Investigative Site 2311 Cypress Texas 90212 —
Connect Investigative Site 2319 San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04700449, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 6, 2024 · Synced Oct 31, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04700449 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →