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Study identifier: NCT07482657 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Phase 2 Study to Investigate the Efficacy and Safety of Zelicapavir in Participants Aged ≥28 Days to ≤36 Months of Age Infected With Respiratory Syncytial Virus

Condition: RSV Infection · RSV · Respiratory Syncytial Virus (RSV)  ·  Sponsor: Enanta Pharmaceuticals, Inc

PhasePhase 2
Planned participants150
Who can joinAll sexes, 28 Days to 36 Months
Healthy volunteersNo

About this study

Zelicapavir is a novel, orally administered, nonfusion replication inhibitor of RSV. It is being investigated in this Phase 2 study (EDP 938-203) as a potential treatment for RSV infection in both hospitalized and non-hospitalized children aged ≥28 days to ≤36 months who present with symptomatic RSV infection.

This description comes directly from the study's public registry record.

Talk to the study team

Enanta Pharmaceuticals, Inc  ·  617 607-0800  ·  charris@enanta.com

Always discuss trial participation with your own doctor first.

Locations (8)

Center of Excellence for Pediatric Infectious Diseases and Vaccines Faculty of Medicine, Chulalongkorn University (CE-PID)Bangkok, ThailandRecruiting
Nakornping HospitalChiang Mai, ThailandRecruiting
Maharaj Nakorn Chiang Mai HospitalChiang Mai, ThailandRecruiting
Chiangrai Prachanukroh HospitalChiang Rai, ThailandRecruiting
Khon Kaen HospitalKhon Kaen, ThailandRecruiting
Lampang HospitalLampang, ThailandRecruiting
Lamphun HospitalLamphun, ThailandRecruiting
Maha Sarakham HospitalMaha Sarakham, ThailandRecruiting

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Source record: clinicaltrials.gov/study/NCT07482657