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NCT06204679 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetics of Fixed-Dose Combination Tablet of Bemnifosbuvir and Ruzasvir

A Phase 1 study, sponsored by Atea Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
42
Enrollment target

NCT06204679: Completed Phase 1 study, sponsored by Atea Pharmaceuticals.

NCT06204679 is a Phase 1 study that has completed, run by Atea Pharmaceuticals. The registered enrollment target is 42 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06204679, a Phase 1 study, has completed, sponsored by Atea Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
42 participants
Enrollment target

Study Summary

This study will assess comparative bioavailability and effect of food on a prototype fixed-dose combination (FDC) of Bemnifosbuvir (BEM) and Ruzasvir (RZR) in healthy subjects

Primary Outcome

Maximum plasma concentration (Cmax)

Interventions

  • DRUG Bemnifosbuvir (BEM)/Ruzasvir (RZR) FDC under fasting conditions
  • DRUG Bemnifosbuvir (BEM)/Ruzasvir (RZR) FDC under fed conditions
  • DRUG Bemnifosbuvir (BEM) and Ruzasvir (RZR) as reference formulation under fasting conditions

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2023-12-14
Est. Completion 2024-08-25
Phase Phase 1
Atea Pharmaceuticals

12 total trials

What the finished NCT06204679 record still lists

NCT06204679 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower).

The record links to 0 conditions, and to 3 interventions - of which Bemnifosbuvir (BEM)/Ruzasvir (RZR) FDC under fasting conditions is the first listed.

NCT06204679 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06204679 about?

NCT06204679 is a clinical study titled "Pharmacokinetics of Fixed-Dose Combination Tablet of Bemnifosbuvir and Ruzasvir". This study will assess comparative bioavailability and effect of food on a prototype fixed-dose combination (FDC) of Bemnifosbuvir (BEM) and Ruzasvir (RZR) in healthy subjects

What is the current status of trial NCT06204679?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2023-12-14. Estimated completion is 2024-08-25.

What interventions are being tested in trial NCT06204679?

The interventions under investigation include: Bemnifosbuvir (BEM)/Ruzasvir (RZR) FDC under fasting conditions (DRUG), Bemnifosbuvir (BEM)/Ruzasvir (RZR) FDC under fed conditions (DRUG), Bemnifosbuvir (BEM) and Ruzasvir (RZR) as reference formulation under fasting conditions (DRUG).

Who is sponsoring clinical trial NCT06204679?

This trial is sponsored by Atea Pharmaceuticals, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06204679's enrollment target sits among peer trials

42 1105th of 2000 higher than 876 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 NCT06204679, the US trial registry maintained by the National Library of Medicine. NCT06204679 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.