Growth HormoneFDA ApprovedFDA Approved

Tesamorelin

Also known as Egrifta, Egrifta WR, Egrifta SV, TH9507, Tesamorelin F8

An FDA-approved GHRH analog used to reduce excess abdominal fat in HIV-infected patients with lipodystrophy.

FDA Approved - HIV lipodystrophy (March 2025: F8 formulation approved)

Regulatory Pathway

Preclinical
Phase I
Phase II
Phase III
Phase IV
Approved

Dosing Protocol

Typical Dose

2 mg daily (F8: 1.28 mg daily)

Frequency

Once daily

Duration

Indefinite for approved indication

Community-reported dosing. Individual results vary. Not a medical recommendation.
Typical community protocol: 2 mg daily (F8: 1.28 mg daily) via Subcutaneous injection, Once daily. Dose range: 1.28-2 mg daily. Duration: Indefinite for approved indication.

Timing & Administration

Administer via Subcutaneous injection. Frequency: Once daily.

Mechanism of Action

A stabilized analog of human GHRH that stimulates the pituitary to release growth hormone. Specifically reduces visceral adipose tissue (VAT) while having minimal effect on subcutaneous fat.

Research Summary

Evidence level: fda approved. Clinical status: FDA Approved - HIV lipodystrophy (March 2025: F8 formulation approved).

Side Effects & Safety

Important Warnings

  • Increased diabetes risk
  • Rare anaphylaxis.
Injection site reactions
joint pain
peripheral edema
pain in extremities
muscle pain
increased diabetes risk
elevated blood glucose
allergic reactions including anaphylaxis

References

No references available.