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Completed Phase 2 Interventional Results available

Safety, Efficacy, and Tolerability Study of PF-06480605 in Subjects With Moderate to Severe Ulcerative Colitis.

ClinicalTrials.gov ID: NCT02840721

Public ClinicalTrials.gov record NCT02840721. 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 24, 2026, 6:50 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 PHASE 2A, MULTICENTER, SINGLE ARM, OPEN- LABEL, TWO-STAGE, STUDY TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY AND PHARMACOKINETICS OF PF-06480605 IN SUBJECTS WITH MODERATE TO SEVERE ULCERATIVE COLITIS

Brief summary

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

The purpose of this study is to evaluate the safety, tolerability, and efficacy of PF-06480605 in subjects with moderate to severe ulcerative colitis.

Study identification

NCT ID
NCT02840721
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Telavant, Inc.
Industry
Enrollment
50 participants

Conditions and interventions

Interventions

Drug

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
Oct 26, 2016 (Actual)
Primary completion
May 31, 2018 (Actual)
Completion
Aug 30, 2018 (Actual)
Last update posted
Oct 23, 2023

2016 – 2018

United States locations

U.S. sites
12
U.S. states
4
U.S. cities
8
Facility City State ZIP Site status
Surgery Center of Aventura Aventura Florida 33180 —
Venture Ambulatory Surgical Center North Miami Beach Florida 33162 —
FQL Research, LLC Pembroke Pines Florida 33027 —
Brigham and Women's Hospital Boston Massachusetts 02115 —
Brigham and Women's Hospital Chestnut Hill Massachusetts 02467 —
NYU Langone Long Island Clinical Research Associates Great Neck New York 11021 —
NYU Langone Nassau Gastroenterology Associates Great Neck New York 11021 —
New York Presbyterian Hospital-Weill Cornell Medical College New York New York 10021 —
Weill Cornell Medical College New York New York 10021 —
Weill Cornell Medicine New York New York 10021 —
New York Presbyterian Hospital New York New York 10065 —
Allegiance Research Specialists, LLC Wauwatosa Wisconsin 53226 —

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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02840721, 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 Oct 23, 2023 · Synced Oct 24, 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 NCT02840721 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →