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Long-Term Follow-Up Safety Monitoring of Patients Dosed in the First-in-Man Phase I/II Study of TT-034.

Hepatitis C Clinical Trial

Official title:
Follow-up to Study Protocol B2801001, A Phase I/II, Open-Label Dose Escalation Study to Evaluate the Safety and Efficacy of Single Doses of TT-034 in Patients With Chronic Hepatitis C [CHC] Infection

Clinical Trial Summary

This is a long-term safety follow-up protocol for subjects who received TT-034 under the B2801001 protocol and consists of monitoring for at least 4.5 years.

Clinical Trial Description

The main purpose of this follow-up study is to detect events suggestive of delayed adverse effects of the study drug by review of clinical histories and discussion with subjects to identify/elicit significant medical events, including but not limited to hematologic, malignant, autoimmune, neurologic, and hepatic events. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02315638
Study type Observational
Source Tacere Therapeutics, Inc.
Contact
Status Terminated
Phase
Start date November 2014
Completion date September 24, 2018
View Details
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