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NCT03800173 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Single Dose Safety, Tolerability and Pharmacokinetics of IV BCX4430
A Phase 1 study, sponsored by BioCryst Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
NCT03800173: Completed Phase 1 study, sponsored by BioCryst Pharmaceuticals.
NCT03800173 is a Phase 1 study that has completed, run by BioCryst Pharmaceuticals. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03800173, a Phase 1 study, has completed, sponsored by BioCryst Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
Study Summary
This is a placebo-controlled, randomized, double-blind study to evaluate the pharmacokinetics of galidesivir following administration of single doses by IV infusion
Primary Outcome
Any event reported on the subject's study record that occurred on or after the initiation of study drug was defined as treatment emergent (TEAE).
Interventions
- DRUG placebo
- DRUG galidesivir
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2018-12-10 |
| Est. Completion | 2019-04-30 |
| Phase | Phase 1 |
What the finished NCT03800173 record still lists
NCT03800173 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).
The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.
NCT03800173 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03800173 about?
NCT03800173 is a clinical study titled "A Study to Evaluate the Single Dose Safety, Tolerability and Pharmacokinetics of IV BCX4430". This is a placebo-controlled, randomized, double-blind study to evaluate the pharmacokinetics of galidesivir following administration of single doses by IV infusion
What is the current status of trial NCT03800173?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2018-12-10. Estimated completion is 2019-04-30.
What interventions are being tested in trial NCT03800173?
The interventions under investigation include: placebo (DRUG), galidesivir (DRUG).
Who is sponsoring clinical trial NCT03800173?
This trial is sponsored by BioCryst Pharmaceuticals, which has 29 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03800173's enrollment target sits among peer trials
32 1296th of 2000 higher than 679 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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