U.S., June 18 -- ClinicalTrials.gov registry received information related to the study (NCT07653100) titled 'A Phase 3 Study in India to Describe the Safety and Immunogenicity of RSVpreF' on June 11.
Brief 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.
Study Start Date: June 22
Study Type: INTERVENTIONAL
Condition:
Respiratory Syncytial Virus (RSV)
Intervention:
BIOLOGICAL: RSVpreF
RSVpreF Vaccine
BIOLOGICAL: Placebo
Placebo
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Pfizer
Published by HT Digital Content Services with permission from Health Daily Digest....