TrialSignal
Clinical trial intelligence report
Immunogenicity of a Third Dose of Either the Moderna COVID-19 Vaccine or Pfizer-BioNTech COVID-19 Vaccine in Kidney Transplant Recipients Who Failed to Respond After Two Previous Doses
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT04969263-Jul 28, 2026
NCT ID
NCT04969263
Status
COMPLETED
Phase
Phase 2
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Executive brief
Investment-Ready Snapshot
The study investigates the immunogenicity of a third dose of mRNA COVID-19 vaccines (Moderna and Pfizer-BioNTech) in kidney transplant recipients who exhibited inadequate antibody responses after two doses. Given the increasing recognition of vulnerable populations, such as transplant recipients, this research addresses a critical gap in COVID-19 vaccination strategies. The results could inform future vaccine recommendations and potentially expand market opportunities for mRNA vaccine manufacturers. The competitive landscape includes ongoing studies by other institutions focusing on similar populations, which may influence market positioning and pricing strategies. Diligence should consider the regulatory landscape and potential for expanded indications based on study outcomes.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04969263
Indication
Kidney Transplant Recipients
Modality
vaccine
Target
SARS-CoV-2 Spike Protein (Receptor Binding Domain)
Intervention
BNT162b2 vaccine (Pfizer/BioNTech), mRNA-1273 vaccine (Moderna)
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.