Peptide library

Reference entry · N-terminally modified GHRH(1-44) analog

Tesamorelin

Also known as: TH9507 · Egrifta · GHRH(1-44) analog

Class
N-terminally modified GHRH(1-44) analog
Size
44 amino acids
Primary targets (literature)
GHRH receptor → pituitary GH / IGF-1 axis
Regulatory context
FDA-approved as Egrifta for a specific HIV lipodystrophy indication. RUO catalog tesamorelin is not approved drug product without verified pharmaceutical sourcing.

Overview

Tesamorelin is an FDA-approved GHRH analog studied in phase 3 trials for HIV-associated lipodystrophy with excess visceral adipose tissue. Catalog material is a distinct RUO supply chain from pharmaceutical Egrifta.

Mechanism in research literature

GHRH receptor agonism stimulates pituitary GH release and downstream IGF-1. N-terminal trans-3-hexenoyl modification extends half-life relative to native GHRH(1-44).

Common research focus areas

  • Phase 3 VAT reduction in HIV lipodystrophy trials
  • Long-term safety and immunogenicity monitoring
  • Comparison with shorter GHRH fragments (sermorelin, mod GRF)
  • MS identity for 44-mer with N-terminal lipid modification

Full literature roundup

Read the cited research summary

An FDA-approved GHRH(1-44) analog with published phase 3 human data in HIV-associated lipodystrophy. What the clinical literature reports — and how catalog material differs.

Tesamorelin research roundup · 6 min

Evaluate catalog material

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Community content — not medical advice. Research use only; nothing here is instruction for human use.