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IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Exenatide

FDA approved · Rx

GLP-1 receptor agonist

Also known as: Byetta, Bydureon, Bydureon Pen, Exendin 4, PT302, exenatidum, Exendin 4 (Heloderma suspectum)

Evidence score
95/ 100
Strong evidence

Strong, human-grade evidence

  • Regulatory standing. FDA-approved prescription medicine
  • Human trials. Backed by controlled human studies
  • Registered human trials. 379 registered studies on ClinicalTrials.gov, most advanced Phase 4
  • 2 cited sources. Includes primary / regulatory sources

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

Exenatide is a synthetic version of exendin-4, a 39 amino acid peptide first found in the saliva of the Gila monster lizard. It activates the GLP-1 receptor, which increases glucose-dependent insulin release, lowers glucagon, and slows stomach emptying. It is sold under brand names including Byetta and Bydureon.

What the evidence shows

Automatic summaryHuman trials

Exenatide is FDA approved for improving blood sugar control in adults with type 2 diabetes, supported by hundreds of registered human trials reaching Phase 4. Uses outside that approved indication, such as for weight loss alone or neurological conditions, remain under study and are not established.

Key facts

Molecular formula
C184H282N50O60S
Molecular weight
4187 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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