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NCT01801293 · ClinicalTrials.gov registry record · Phase 1
A Phase 1 Study to Evaluate the Pharmacokinetics, Metabolism, and Excretion of GS-5806
A Phase 1 study, sponsored by Gilead Sciences.
- Completed
- Registry status
- Phase 1
- Development phase
- 8
- Enrollment target
NCT01801293: Completed Phase 1 study, sponsored by Gilead Sciences.
NCT01801293 is a Phase 1 study that has completed, run by Gilead Sciences. The registered enrollment target is 8 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01801293, a Phase 1 study, has completed, sponsored by Gilead Sciences.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 8 participants
- Enrollment target
Study Summary
This is a single center, open-label, Phase 1 study to determine the mass balance of of GS-5806 following administration of a single, oral dose of radiolabeled \[14C\]-GS-5806 in healthy subjects.
Primary Outcome
The primary outcome measure of this study is the urine and fecal recovery of total \[14C\]-radioactivity.
Interventions
- DRUG GS-5806
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2013-03 |
| Est. Completion | 2013-04 |
| Phase | Phase 1 |
What the finished NCT01801293 record still lists
NCT01801293 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower).
The record links to 0 conditions, and to 1 intervention - of which GS-5806 is the first listed.
NCT01801293 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01801293 about?
NCT01801293 is a clinical study titled "A Phase 1 Study to Evaluate the Pharmacokinetics, Metabolism, and Excretion of GS-5806". This is a single center, open-label, Phase 1 study to determine the mass balance of of GS-5806 following administration of a single, oral dose of radiolabeled \[14C\]-GS-5806 in healthy subjects.
What is the current status of trial NCT01801293?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 8 participants. The study started on 2013-03. Estimated completion is 2013-04.
What interventions are being tested in trial NCT01801293?
The interventions under investigation include: GS-5806 (DRUG).
Who is sponsoring clinical trial NCT01801293?
This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01801293's enrollment target sits among peer trials
8 1959th of 2000 higher than 29 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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