Growth Hormone

Tesamorelin

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

FDA Approved
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Key Facts: Tesamorelin

Category
Growth Hormone
FDA Status
FDA Approved
Clinical Status
FDA Approved - HIV lipodystrophy (March 2025: F8 formulation approved)
Administration
Subcutaneous injection
Typical Dose
2 mg daily (F8: 1.28 mg daily)
Frequency
Once daily
Duration
Indefinite for approved indication
Also Known As
Egrifta, Egrifta WR, Egrifta SV, TH9507, Tesamorelin F8

Mechanism of Action

Tesamorelin is a stabilized analog of human GHRH that stimulates the pituitary to release growth hormone. It specifically reduces visceral adipose tissue (VAT) while having minimal effect on subcutaneous fat, likely through GH-mediated lipolysis.

Research Summary

FDA approved based on trials showing 15-20% reduction in visceral adipose tissue over 26 weeks. March 2025: FDA approved new F8 formulation (Egrifta WR) with weekly reconstitution, reducing patient burden. CROI 2025 data highlighted limitations of BMI for cardiovascular risk assessment in HIV patients.

Trial Progress:FDA Approved
Pre
I
II
III
IV
FDA

Dosing Information

FDA Approved·Human clinical trials completed, FDA approved

Typical Dosing

Community experience

Common Dose

2 mg daily (F8: 1.28 mg daily)

Range

1.28-2 mg daily

Frequency

Once daily

FDA-approved dose is 2 mg (original) or 1.28 mg (F8/Egrifta WR formulation). Inject subcutaneously in abdomen. F8 requires weekly reconstitution vs daily.

Research Dosing

Scientific studies

FDA-approved dosing

Doses from Studies

Duration

Indefinite for approved indication

Administration

Subcutaneous injection

Timing & Administration

Best Time to Take

Before bed (fasted)

Once daily before bed

Food Recommendation

Take on empty stomach

Why This Timing?

FDA-approved GHRH analog works best on empty stomach, timed with natural GH release during sleep.

Possible Side Effects

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • Injection site reactions (common)
  • Joint pain
  • Peripheral edema
  • Pain in extremities
  • Muscle pain
  • Increased diabetes risk
  • May elevate blood glucose
  • Allergic reactions including anaphylaxis (rare)
  • FDA approved for HIV lipodystrophy

References

Research This Peptide Further

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Tesamorelin from $100/kit

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Frequently Asked Questions

What does Tesamorelin do?

An FDA-approved GHRH analog used to reduce excess abdominal fat in HIV-infected patients with lipodystrophy. New F8 formulation (Egrifta WR) approved March 2025 allows weekly reconstitution vs daily.

How does Tesamorelin work?

Tesamorelin is a stabilized analog of human GHRH that stimulates the pituitary to release growth hormone. It specifically reduces visceral adipose tissue (VAT) while having minimal effect on subcutaneous fat, likely through GH-mediated lipolysis.

Is Tesamorelin FDA approved?

Yes, Tesamorelin is FDA approved. FDA Approved - HIV lipodystrophy (March 2025: F8 formulation approved)

What are the side effects of Tesamorelin?

Reported side effects include: Injection site reactions (common), Joint pain, Peripheral edema, Pain in extremities, Muscle pain. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of Tesamorelin?

Community-reported common dose: 2 mg daily (F8: 1.28 mg daily) (Once daily). Range: 1.28-2 mg daily. Administration: Subcutaneous injection. Community-reported doses. Not medical advice. Consult healthcare provider.

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