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NCT01316237 · ClinicalTrials.gov registry record · Phase 1

A Study Evaluating the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-6620 in Treatment Naïve Subjects With Chronic Hepatitis C Virus Infection

A Phase 1 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 1
Development phase
90
Enrollment target

NCT01316237: Completed Phase 1 study, sponsored by Gilead Sciences.

NCT01316237 is a Phase 1 study that has completed, run by Gilead Sciences. The registered enrollment target is 90 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01316237, a Phase 1 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 1
Development phase
90 participants
Enrollment target

Study Summary

A Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Ranging Study Evaluating the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-6620 in Treatment Naïve Subjects with Chronic Hepatitis C Virus Infection.

Interventions

  • DRUG GS-6620

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2011-01
Est. Completion 2012-01
Phase Phase 1
Gilead Sciences

504 total trials

What the finished NCT01316237 record still lists

NCT01316237 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% higher).

The record links to 0 conditions, and to 1 intervention - of which GS-6620 is the first listed.

NCT01316237 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01316237 about?

NCT01316237 is a clinical study titled "A Study Evaluating the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-6620 in Treatment Naïve Subjects With Chronic Hepatitis C Virus Infection". A Double-Blind, Randomized, Placebo-Controlled, Multiple Dose Ranging Study Evaluating the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-6620 in Treatment Naïve Subjects with Chronic Hepatitis C Virus Infection.

What is the current status of trial NCT01316237?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 90 participants. The study started on 2011-01. Estimated completion is 2012-01.

What interventions are being tested in trial NCT01316237?

The interventions under investigation include: GS-6620 (DRUG).

Who is sponsoring clinical trial NCT01316237?

This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01316237's enrollment target sits among peer trials

90 628th of 2000 higher than 1,352 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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Source: ClinicalTrials.gov NCT01316237, the US trial registry maintained by the National Library of Medicine. NCT01316237 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.