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NCT06585150

Study of Obeldesivir to Treat Nonhospitalized Adults With Acute Respiratory Syncytial Virus (RSV) Infection

Terminated Phase 2 Last updated 28 July 2025
What this trial tests

Phase 2 trial testing Obeldesivir in RSV Infection in 150 participants. Terminated before completion.

Timeline
14 October 2024
Primary endpoint
8 May 2025
9 June 2025

Quick facts

Lead sponsorGilead Sciences
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment150
Start date14 October 2024
Primary completion8 May 2025
Estimated completion9 June 2025
Sites121 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Gilead Sciences — full company profile →

Who can join

18 and older, any sex, with RSV Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical study is to learn more about the study drug, obeldesivir (ODV; GS-5245), and how safe and effective it is in treating nonhospitalized adults with acute respiratory syncytial virus (RSV) infection. The researchers want to see if obeldesivir can help participants' symptoms get better faster. The primary objectives of this study are to evaluate the efficacy of ODV in reducing the duration of symptoms and to evaluate the safety and tolerability of ODV in nonhospitalized adult participants with acute RSV infection.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Oral dosing of the nucleoside analog obeldesivir is efficacious against RSV infection in African green monkeys.
    Pitts J, Zamora JLR, Manhas S, Aeschbacher T, et al · · 2025 · cited 1× · PMID 40645925 · DOI 10.1038/s41467-025-61595-3

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Other trials of Obeldesivir

Trials testing the same drug.

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Other Gilead Sciences trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06585150.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing