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Clinical Trials in the EU / 2025-524034-26-02
Authorised, recruiting Phase I

A randomized, placebo-controlled trial, to evaluate the safety, immunogenicity and the optimal dose of MOPEVAC-Las vaccine candidate against Lassa Fever, in healthy volunteers consisting of an unblinded dose escalation and a blinded treatment phase (FIRST-IN-MOP)

2025-524034-26-02 · tracked via the Priya Life Science EU tracker
Sponsor
Institut Pasteur
Sponsor type
Educational Institution
Therapeutic area
Virus Diseases
Decision date
01/09/2026
Enrollment target
72
Sites
France

Condition studied

Lassa fever

Eligibility

Age group
18-64 years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-524034-26-02 on CTIS ↗ ← All trials in the EU