A Phase 1B, Randomized, Placebo-Controlled, Double-Blind, Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Q203 When Administered Orally to Healthy Adult Subjects
Latest Information Update: 15 Dec 2022
At a glance
- Drugs Telacebec (Primary)
- Indications Tuberculosis
- Focus Adverse reactions
- Sponsors Qurient Co
- 12 Dec 2022 Results assessing Safety, Tolerability, Pharmacokinetics, and Metabolism of Telacebec (Q203) for the Treatment of Tuberculosis published in the Antimicrobial Agents and Chemotherapy
- 11 May 2018 Status changed from active, no longer recruiting to completed.
- 10 Apr 2018 Planned primary completion date changed from 1 Dec 2017 to 1 May 2018.