A Phase 3 Study in India to Describe the Safety and Immunogenicity of RSVpreF
NCT07653100 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 540
Last updated 2026-07-29
Summary
The purpose of this phase 3 multicenter, double-blinded, placebo-controlled study in India is to learn about the safety and immunogenicity of RSVpreF in adults.
Conditions
- Respiratory Syncytial Virus (RSV)
Interventions
- BIOLOGICAL
-
RSVpreF
RSVpreF Vaccine
- BIOLOGICAL
-
Placebo
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-06-22
- Primary Completion
- 2027-01-25
- Completion
- 2027-01-25
- FDA Drug
- Yes
Countries
- India
Study Locations
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