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Clinical trial intelligence report
A Non-Randomized, Open Label, Controlled, Dose-Escalation, Phase I Clinical Trial to Evaluate the Safety, Reactogenicity and Immunogenicity of One or Two Administrations of Candidate Rabies mRNA Vaccine CV7202 in Healthy Adult Subjects
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 25, 2026
Report code
NCT03713086-Jun 25, 2026
NCT ID
NCT03713086
Status
COMPLETED
Phase
Phase 1
Sponsor
CureVac
Executive brief
Investment-Ready Snapshot
CureVac's CV7202 is an innovative mRNA-based rabies vaccine currently in Phase 1 clinical trials. The vaccine aims to provide a safer and potentially more effective alternative to traditional rabies vaccines. The market for rabies vaccines is significant, particularly in regions with high rabies incidence. Competitive advantages may arise from the use of mRNA technology, which has shown promise in rapid vaccine development and adaptability. However, the company must navigate existing patents and regulatory pathways to ensure successful market entry. The completion of this trial could position CureVac favorably against established players in the rabies vaccine market.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03713086
Indication
Rabies
Modality
protein therapy
Target
Rabies virus antigens via mRNA technology
Intervention
Rabipur®, Rabies mRNA vaccine CV7202, Rabies mRNA vaccine CV7202, Rabies mRNA vaccine CV7202
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.