drugset / Trial / NCT03891420
A Study to Evaluate the Safety, Pharmacokinetics and Antiviral Effects of Galidesivir in Yellow Fever or COVID-19
Phase 1
Terminated
24 enrolled
BioCryst Pharmaceuticals
National Institute of Allergy and Infectious Diseases (NIAID) · collab
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a placebo-controlled, randomized, double-blind study to evaluate the pharmacokinetics, safety and antiviral activity of galidesivir in subjects with yellow fever (YF) or COVID-19.
Timeline
- Start
- 2020-04-09
- Primary completion
- 2021-01-31
- Completion
- 2021-04-30
Outcome
Met primary endpoint
Stopped (Business): “Sponsor decision to no longer pursue indications studied in this trial”
release “Part 1 of a clinical trial of its broad-spectrum antiviral, galidesivir, showed that galidesivir was safe and generally well tolerated in patients infected with SARS-CoV-2” biocryst.com ↗
release “No safety signals were identified, and all three dose levels were equally safe.” biocryst.com ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Galidesivir | Small molecule | — | Intravenous |