Tesamorelin
Also known as: Egrifta, Egrifta WR, Egrifta SV, TH9507, Tesamorelin F8
At a glance
PeptiGuide dataset · reviewed Aug 2026
What it is
FDA-approved GHRH analog for HIV-associated visceral fat reduction
Status
FDA Approved
Typical dose
2mg
Researched for
Visceral fat reduction, body composition, HIV lipodystrophy
Trial progress
- PrePreclinical
- IPhase I
- IIPhase II
- IIIPhase III
- IVPhase IV
- FDAFDA approved
FDA approved - FDA-approved for specific uses with established human evidence
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In plain language
- Tesamorelin is a single- GHRH analog with FDA-approved status for excess visceral abdominal fat in HIV-associated lipodystrophy.
- The source lists Egrifta, Egrifta WR, Egrifta SV, TH9507, and Tesamorelin F8 as aliases.
- Extracted dose information includes 2 mg daily, with F8 listed at 1.28 mg daily, given by injection.
- Research areas reported by the source include visceral fat reduction, body composition, and HIV lipodystrophy.
- The source cautions that evidence is stronger for the approved HIV-associated indication than for broader general fat-loss or anti-aging uses.
How it's thought to work
Tesamorelin is presented as a stabilized analog of GHRH 1-44. It acts at GHRH receptors upstream of direct growth-hormone replacement, prompting pituitary growth-hormone release and subsequent IGF-1 signaling. The source reports an N-terminal trans-3-hexenoic acid modification that slows enzymatic degradation, extending the signal relative to native GHRH. Trial-observed visceral-fat reductions are attributed to this growth-hormone-axis activity.
What the research shows
Where the research stands
The source describes an approval package grounded in randomized, placebo-controlled human studies. It specifically names Falutz and colleagues in a 2007 New England Journal of Medicine publication, reporting six-month visceral abdominal fat reduction in HIV patients, lipid-profile improvement, and no meaningful worsening of blood-sugar control. It also cites later randomized work, including a JAMA-published study led by Stanley, with reported reductions in visceral fat and liver fat. A smaller placebo-controlled study in non-HIV adults with abdominal obesity is described as showing visceral-fat reduction over 26 weeks, but the source frames that broader setting as less established than the HIV-associated indication. Reported cautions include joint pain, swelling, IGF-1 increases, cancer-history concerns, and uncontrolled diabetes concerns for growth-hormone-axis drugs.
What it shows
✓ Human clinical evidence
FDA-approved for specific uses with established human evidence
△ Limitations
Use only according to approved labeling and qualified medical guidance.
Bottom line: FDA Approved - HIV lipodystrophy (March 2025: F8 formulation approved) FDA Approved
Typical dosing
CommunityCommunity dataset2 mg
daily (F8: 1.28 mg daily)
Community-reported row preserves the source range. The source also notes original FDA-approved dosing at 2 mg and F8/Egrifta WR at 1.28 mg, with F8 requiring weekly reconstitution rather than daily reconstitution. · Subcutaneous injection in abdomen
Research dosing
Indication-specificApproved for specific uses - study doses are indication-specific
Timing & administration
Best time to take
Before bed while fasted
Once daily before bed
Food recommendation
Take on empty stomach
Why this timing?
The source connects bedtime, fasted use with the sleep period when natural growth-hormone release is expected to occur.
Possible side effects
Not everyone experiences these. Individual responses vary with dose, duration, and personal factors.
- Injection site reactions
- Joint pain
- Peripheral edema
- Pain in extremities
- Muscle pain
- Increased diabetes risk
- May elevate blood glucose
- Allergic reactions including anaphylaxis
- Increased IGF-1
Not everyone experiences side effects, and severity can vary by context, purity, route, and individual health factors.
Sources
Frequently asked questions
Sequence
trans-3-hexenoyl-YADAIFTNSYRKVLGQLSARKLLQDIMSRQQGESNQERGARARL-NH2
One open dataset
Every fact on this page - doses, side effects, references - comes from the same PeptiGuide dataset that powers the Tracker, Compare, and the Lab.
Browse the datasetEducational resource, not medical advice. Talk to your clinician before acting on anything here.
Community discussion
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