AVIR

Atea Pharmaceuticals, Inc.

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5Trials in this database
4Recorded changes · last 12 months
Partial coverageOnly the trials and history collected so far

Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.

Completion dates · Pro

Which trial dates moved later?

Pro summarizes how far estimated completion dates moved later and counts trials with edits to their main study measures, using the history available here. View Pro features
TrialSponsorPhaseStatusPrimary completion
Study of AT-752 in Patients With Dengue InfectionNCT05466240AVIRPhase 2Terminated2023-01-19Actual
SUNRISE-3: Efficacy and Safety of Bemnifosbuvir in High-Risk Outpatients With COVID-19NCT05629962AVIRPhase 3Completed2024-04-25Actual
A Phase 2, Safety and Efficacy of Bemnifosbuvir (BEM) and Ruzasvir (RZR) in Subjects With Chronic HCVNCT05904470AVIRPhase 2Completed2024-12-09Actual
C-BEYOND: Efficacy and Safety of BEM/RZR vs. SOF/VEL in Subjects With Chronic HCVNCT06868264AVIRPhase 3Active not recruiting2026-09Estimated
C-Forward: Efficacy and Safety of BEM/RZR vs SOF/VEL in Subjects With Chronic HCVNCT07037277AVIRPhase 3Active not recruiting2026-12Estimated

Latest recorded trial changes

· 1 field changed

Main study measure wording changed

Text changed; whether the study measures changed has not been verified. Saved text may be shortened.

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− Before

Measure: Proportion of Subjects Achieving Sustained Virologic Response at 12 Weeks Post-treatment (SVR12)

+ After

Measure: Percentage of Subjects Achieving Sustained Virologic Response at 12 Weeks Post-treatment (SVR12)

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· 1 field changed

Main study measure wording changed

Text changed; whether the study measures changed has not been verified. Saved text may be shortened.

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− Before

Measure: Proportion of subjects experiencing treatment-emergent adverse events Measure: Proportion of subjects achieving sustained virologic response at 12 weeks post-treatment (SVR12)

+ After

Measure: Proportion of Subjects Achieving Sustained Virologic Response at 12 Weeks Post-treatment (SVR12)

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