Drug intelligence / Profile preview

BPI viper antivenom

Development stage
Phase 2
Lead developer
Burma Pharmaceutical Industry
Modality
Recombinant Proteins and Enzymes, Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

BPI viper antivenom is a lyophilized (freeze-dried) monospecific F(ab)2 fragment-based equine-derived immunoglobulin preparation developed for the treatment of envenoming by Russell’s viper (*Daboia siamensis*) in Myanmar. It was developed as part of a collaborative initiative to improve access to effective snakebite therapy in regions with limited electrification and healthcare infrastructure. The product contains purified F(ab)2 antibody fragments that specifically bind and neutralize Russell’s viper venom toxins, facilitating their redistribution away from target tissues and elimination from the body. The mechanism of action involves direct binding to venom components, thereby preventing or reversing toxic effects such as coagulopathy and tissue damage. The drug is produced using hyper-immune horse plasma at GMP-compliant facilities operated by Burma Pharmaceutical Industry (BPI). It has replaced previous liquid formulations due to improved stability and ease of distribution[4][5][6][10].

Brand names
BPI viper antivenom
Other names
Lyophilized BPI viper antivenomfreeze-dried anti-snake venom (BPI)monospecific lyophilised F(ab)2 antivenom (Viper antivenom BPI)
02

Targets

vvPLA2 (Russell's viper venom phospholipase A2)SVSP (Snake venom serine protease)RVV-X (Russell's viper venom factor X activator)

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