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NCT06684431: CCHF-NP-1

Study to Evaluate Safety and Immunogenicity of DNA Vaccine N-pVAX1 Against Crimean Congo Hemorrhagic Fever

Completed Phase 1 Last updated 23 March 2026
What this trial tests

Phase 1 trial testing N-pVAX1 in Crimean Congo Hemorrhagic Fever in 15 participants. Completed in 17 March 2026.

Timeline
12 November 2024
Primary endpoint
17 March 2026
17 March 2026

Quick facts

Lead sponsorKarolinska Institutet
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment15
Start date12 November 2024
Primary completion17 March 2026
Estimated completion17 March 2026
Sites1 location across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Karolinska Institutet

Who can join

Adults 18 to 60, any sex, with Crimean Congo Hemorrhagic Fever. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This First-in-human dose-escalation vaccine phase I study aims to evaluate safety and reactogenicity of the investigational vaccine N-pVAX1, against Crimean Congo Hemorrhagic Fever, delivered by in vivo EP given as three im doses at weeks 0, 4 and 12.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Karolinska Institutet trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06684431.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing