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Botulinum Antitoxin Heptavalent

Plasma-derived product · Antagonist of botulinum toxin A, botulinum toxin B and botulinum toxin C · developed by Emergent BioSolutions

Phase 1 Most advanced trial (none active)

EBS Developer

1 Registered trials

What is Botulinum Antitoxin Heptavalent?

Botulinum Antitoxin Heptavalent (BAT) is an equine-derived plasma product containing antibodies against seven botulinum toxin serotypes (A-G). It neutralizes botulinum toxins and is studied for treatment of botulism.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as: Botulism Antitoxin (BAT)
Drug type: Plasma-derived product
Targets: botulinum toxin A, botulinum toxin B, botulinum toxin C, botulinum toxin D, botulinum toxin E, botulinum toxin F
Mechanism: Antagonist of botulinum toxin A, botulinum toxin B and botulinum toxin C
Therapy area: Infectious disease
Developer: Emergent BioSolutions (EBS)
FDA status: Investigational, not approved in the US. Most advanced trial: Phase 1

🧪 Clinical trials

Trial	Phase	Condition	Status	Sponsor
NCT00360737	Phase 1	Healthy	Completed	EBS

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Healthy

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Sources

ClinicalTrials.gov NCT00360737

Updated Oct 3, 2026. Something wrong or missing? Report it on the EBS page.

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Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z