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HormoneFDA Approved

Tesamorelin (Egrifta)

Subcutaneous injection (daily)
Written by Peptide Association Editorial TeamMedically reviewed by Ian Justl Ellis, MD, CPTLast reviewed Editorial policy

Overview

A synthetic GHRH analog consisting of the 44-amino acid sequence of human GHRH with a trans-3-hexenoic acid modification at the N-terminus to improve stability. Tesamorelin specifically targets visceral adipose tissue reduction by stimulating lipolysis through GH-mediated pathways.

Mechanism of Action

It is the only FDA-approved treatment for HIV-associated lipodystrophy.

Research Summary & Key Findings

FDA-approved in 2010 for reduction of excess abdominal fat in HIV-infected patients with lipodystrophy. Clinical trials showed 15-18% reduction in visceral adipose tissue. Also demonstrated improvements in liver fat content in patients with NAFLD in Phase 2 studies.

Clinical Status

FDA Approved

Tesamorelin (Egrifta) has received FDA approval and is available for clinical use under appropriate medical supervision. Consult a qualified healthcare provider for prescribing information.

Administration Routes

Subcutaneous injection (daily)

References

Primary literature

Study-level citations for this compound are being verified against the primary sources before publication. The database queries above return the current indexed literature in the meantime.

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Disclaimer: This information is provided for educational and research purposes only. It is not intended as medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before starting any peptide therapy. The Peptide Association does not endorse or recommend any specific treatment protocol. See our editorial policy for how this content is produced and reviewed.