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Study identifier: NCT07659002 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Polyvalent Antivenom (Premium-PANAF) for Snakebite Envenoming in Ethiopia

Condition: Snake Envenomation  ·  Sponsor: Medecins Sans Frontieres, Netherlands

PhaseN/A
Planned participants600
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

Snakebite Envenomation is recognised as a Neglected Tropical Diseases with high lethality in Sub-Saharan Africa. The current syndromic treatment approach is also fraught by supply pipeline constraints and need for cold-chain, thus negatively impacting outcomes in resource limited settings. Despite the lack of clinical outcome data from studies in humans, after a comprehensive risk-benefit assessment, the World Health Organisation (WHO), in May 2023, recommended the use of Premium-PANAF polyvalent snake antivenom that is lyophilised, and therefore does not require cold-chain conditions. Médecins Sans Frontières (MSF) also updated its treatment protocol with Premium PANAF being standard of care since June 2025 at Abdurafi (Midre Genet) Health Centre in north west Ethiopia. Real-world effectiveness by means of Phase IV post marketing studies or pharmacovigilance programmes in countries where it has recently been rolled out is not yet available. This prospective observational cohort study, with a capped sample size of 600 patients, would thus provide much needed evidence on the safety and effectiveness of Premium-PANAF in resource limited settings to help inform national and international treatment guidelines.

This description comes directly from the study's public registry record.

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Locations (1)

Abdurafi Health CenterĀbderafī, Amhara, EthiopiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07659002