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Clinical trial intelligence report
Booster Dose of mRNA SARS-CoV-2 Vaccine for Kidney Transplant Recipients Without Adequate Humoral Response With or Without Immunosuppression Reduction - Protocol for a Randomised Controlled Trial (BECAME Study)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT04961229-Jul 28, 2026
NCT ID
NCT04961229
Status
UNKNOWN
Phase
Phase 4
Sponsor
dafna yahav
Executive brief
Investment-Ready Snapshot
The BECAME study, sponsored by Dafna Yahav at Rabin Medical Center, aims to address the inadequate humoral response to mRNA SARS-CoV-2 vaccination in kidney transplant recipients. This population is at heightened risk for severe COVID-19 outcomes, creating a significant market opportunity for enhanced vaccination strategies. The trial compares the efficacy of a third BNT162b2 vaccine dose with and without immunosuppression reduction, potentially leading to improved patient outcomes and increased adoption of booster vaccination protocols. The results could inform clinical guidelines and influence market dynamics for COVID-19 vaccines, particularly in immunocompromised populations. Given the ongoing need for effective vaccination strategies in vulnerable groups, successful outcomes may enhance the competitive positioning of the BNT162b2 vaccine in the market.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04961229
Indication
COVID-19 Acute Respiratory Distress Syndrome
Modality
monoclonal antibody
Target
SARS-CoV-2 spike protein
Intervention
The Pfizer mRNA-based BNT162b2 vaccine
Source record
Protocol Description
Detailed source ingestion pending.
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Outcome Measures
Detailed source ingestion pending.
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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.
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Contacts
Detailed source ingestion pending.