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TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC) | Clinical Trials | Clareo Health

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TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC)

Study 0146: A Phase 1a, Double-Blinded, Randomized, Placebo Controlled, Single Ascending Dose (SAD) Study to Evaluate the Safety, Tolerability, and Systemic Exposure of TD-3504 in Healthy Subjects and Subjects With Ulcerative Colitis (UC)

NCT03103412•Theravance Biopharma

View on ClinicalTrials.gov

Summary

This study is designed to evaluate the safety, tolerability, and pharmacokinetics (PK) of single-dose TD-3504 and single dose 15N2-tofacitinib in healthy subjects and subjects with UC. The relative bioavailability of tofacitinib released from TD-3504 compared to co-administered oral heavy-labeled tofacitinib (15N2-tofacitinib) will also be evaluated.

Eligibility

Age

18 - 55 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•Male or female between 18 to 55 years old
•Male subjects must abstain from sexual intercourse or use a highly effective method of birth control
•Women of child bearing potential must have a negative pregnancy test and either abstain from sex or use a highly effective method of birth control
•Body Mass Index (BMI) 18 to 32 kg/m2
•Willing and able to give informed consent
•Subject has a history of UC
•Subject is either not taking any medication for UC or has been taking a stable dose of ulcerative colitis medications for ≥ 14 days

Exclusion Criteria

•Is positive for hepatitis A, B or C, HIV or tuberculosis
•Has clinically significant abnormalities in baseline laboratory evaluations
•Subject has a clinically significant abnormal electrocardiogram (ECG)
•Participated in another clinical trial of an investigational drug (or medical device) within 30 days prior to screening (or within 60 days prior to screening if investigational drug was a biologic, or is currently participating in another trial of an investigational drug (or medical device)
•Use of prescription drugs or any chronic over the counter medications within 14 days prior to clinic admission or requires continuing use during study participation, with the exception of hormonal contraceptives or hormone replacement therapy or standard daily multivitamin.

Locations (1)

Anaheim Clinical Trials, LLC

Anaheim, California, United States

Key Dates

Start Date

May 4, 2017

Primary Completion Date

November 8, 2017

Completion Date

November 8, 2017

Last Updated

January 14, 2021

Enrollment

ACTUAL participants

Conditions

Active Mild Ulcerative Colitis, Active Moderate Ulcerative Colitis, Healthy Subjects

Interventions

TD-3504

DRUG

15N2-tofacitinib

DRUG

Placebo

DRUG