A Study to Investigate Safety, Tolerability, and PK of Oral Doses of TCK-276 in Patients With Rheumatoid Arthritis

PHASE1CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

August 10, 2022

Primary Completion Date

July 20, 2023

Study Completion Date

July 27, 2023

Conditions
Rheumatoid Arthritis
Interventions
DRUG

TCK-276

Patients will receive an oral dose of TCK-276 QD under fed conditions from Day 1 to Day 7.

DRUG

TCK-276 Placebo

Patients will receive an oral dose of TCK-276 matching placebo QD under fed conditions from Day 1 to Day 7.

Trial Locations (8)

32789

Clinical Site Partners, LLC dba CSP Orlando, Winter Park

33014

San Marcus Research Clinic, Inc., Miami Lakes

33016

Floridian Clinical Research, LLC, Miami Lakes

33136

SouthCoast Research Center, Inc, Miami

33155

Allied Biomedical Research Institute, Miami

33172

St. Jude Clinical Research, LLC, Doral

75149

SMS Clinical Research, LLC, Mesquite

92780

Orange County Research Center, Tustin

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

Teijin America, Inc.

INDUSTRY