Study of AT-752 in Patients With Dengue Infection
Trial details
- Registry ID
- NCT05466240
- Phase
- Phase 2
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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.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| Study of AT-752 in Patients With Dengue InfectionNCT05466240 | AVIR | Phase 2 | Terminated | 2023-01-19Actual |
| SUNRISE-3: Efficacy and Safety of Bemnifosbuvir in High-Risk Outpatients With COVID-19NCT05629962 | AVIR | Phase 3 | Completed | 2024-04-25Actual |
| A Phase 2, Safety and Efficacy of Bemnifosbuvir (BEM) and Ruzasvir (RZR) in Subjects With Chronic HCVNCT05904470 | AVIR | Phase 2 | Completed | 2024-12-09Actual |
| C-BEYOND: Efficacy and Safety of BEM/RZR vs. SOF/VEL in Subjects With Chronic HCVNCT06868264 | AVIR | Phase 3 | Active not recruiting | 2026-09Estimated |
| C-Forward: Efficacy and Safety of BEM/RZR vs SOF/VEL in Subjects With Chronic HCVNCT07037277 | AVIR | Phase 3 | Active not recruiting | 2026-12Estimated |
NCT07037277 · Atea Pharmaceuticals, Inc.
Recruiting
Active not recruiting
NCT06868264 · Atea Pharmaceuticals, Inc.
Recruiting
Active not recruiting
NCT05904470 · Atea Pharmaceuticals, Inc.
Text changed; whether the study measures changed has not been verified. Saved text may be shortened.
Measure: Proportion of Subjects Achieving Sustained Virologic Response at 12 Weeks Post-treatment (SVR12)
Measure: Percentage of Subjects Achieving Sustained Virologic Response at 12 Weeks Post-treatment (SVR12)
NCT05904470 · Atea Pharmaceuticals, Inc.
Text changed; whether the study measures changed has not been verified. Saved text may be shortened.
Measure: Proportion of subjects experiencing treatment-emergent adverse events
Measure: Proportion of subjects achieving sustained virologic response at 12 weeks post-treatment (SVR12)
Measure: Proportion of Subjects Achieving Sustained Virologic Response at 12 Weeks Post-treatment (SVR12)