Study to Assess the Safety and Efficacy of ZX-7101A for Oral Suspension in Chinese Pediatric Participants 2 to 11 Years of Age With Influenza

PHASE3Not yet recruitingINTERVENTIONAL
Enrollment

168

Participants

Timeline

Start Date

October 20, 2025

Primary Completion Date

March 31, 2026

Study Completion Date

April 15, 2026

Conditions
Respiratory Viral Infection
Interventions
DRUG

ZX-7101A for oral suspension

ZX-7101A will be administered as oral suspension in a single dose on Day 1. Oseltamivir phosphate matching placebo will also be administered as oral suspension twice daily (BID) for 5 days.

DRUG

Oseltamivir phosphate for oral suspension

Oseltamivir phosphate will be administered as oral suspension BID for 5 days. Participants receiving oseltamivir will also receive ZX-7101A matching placebo as oral suspension, single dose on Day 1.

All Listed Sponsors
lead

Nanjing Zenshine Pharmaceuticals

INDUSTRY

NCT07095257 - Study to Assess the Safety and Efficacy of ZX-7101A for Oral Suspension in Chinese Pediatric Participants 2 to 11 Years of Age With Influenza | Biotech Hunter | Biotech Hunter