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A PHASE 2B, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL GROUP, DOSE RANGING STUDY OF ORAL PF-06651600 AND PF-06700841 AS INDUCTION AND CHRONIC THERAPY IN SUBJECTS WITH MODERATE TO SEVERE ULCERATIVE COLITIS
The purpose of this study is to determine whether PF-06651600 and PF-06700841 are effective in treatment of moderate to severe ulcerative colitis.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Dothan Surgery Center
Dothan, Alabama, United States
Gut P.C., dba Digestive Health Specialists of the Southeast
Dothan, Alabama, United States
Long Beach Clinical Trials Services Inc.
Long Beach, California, United States
Southern California Research Institute Medical Group/West Gastroenterology Medical Group/Airport En-
Los Angeles, California, United States
Clinical Application Laboratories, INC.
San Diego, California, United States
San Diego Endoscopy Center
San Diego, California, United States
Medical Associates Research Group
San Diego, California, United States
Front Range Endoscopy Center
Colorado Springs, Colorado, United States
Peak Gastroenterology Associates
Colorado Springs, Colorado, United States
Bristol Hospital
Bristol, Connecticut, United States
Start Date
February 3, 2017
Primary Completion Date
May 10, 2021
Completion Date
May 10, 2021
Last Updated
July 21, 2022
319
ACTUAL participants
PF-06651600 or Placebo
DRUG
PF-06700841 or Placebo
DRUG
PF-06700841
DRUG
PF-06651600
DRUG
Lead Sponsor
Pfizer
NCT07271069
NCT06975722
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07185009