Skip to main content
GLP-1 / MetabolicVerified

Tesamorelin

Egrifta

A stabilized growth-hormone-releasing hormone (GHRH) analog that binds pituitary GHRH receptors to stimulate endogenous growth hormone secretion. FDA-approved (Egrifta) to reduce excess visceral abdominal fat in HIV-associated lipodystrophy.

Tesamorelin
Category
GLP-1 / Metabolic
Half-life
~26-38 min, subcutaneous
Common vial
5, 10 mg
Regulatory
FDA approved

Tracking and educational reference only, on values you enter or import yourself. Not medical advice or a dosing recommendation.

01

Regulatory status

FDA approved

The FDA has approved at least one product containing this substance for a specific medical use, which means it has been through the agency review process and carries an approved label. Approval is always for named indications in named populations, so it is not a statement that any other use has been evaluated.

A regulatory status describes paperwork, not safety. An approved compound can still be wrong for a given person, and an unapproved one is neither thereby dangerous nor thereby fine.

02

Half-life

~26-38 min, subcutaneous. Half-life is an educational pharmacology figure, drawn from public sources, and is not a schedule or dosing instruction.

03

Storage & handling

Supplied lyophilized; reconstitute with sterile water; refrigerate the finished product and protect from light.

04

References

  • FDA label: Egrifta (2010)

Read the source

Common questions

Tesamorelin, answered plainly.

01What is Tesamorelin?+

A stabilized growth-hormone-releasing hormone (GHRH) analog that binds pituitary GHRH receptors to stimulate endogenous growth hormone secretion. FDA-approved (Egrifta) to reduce excess visceral abdominal fat in HIV-associated lipodystrophy. It is also referred to as Egrifta. It is listed here under GLP-1 / Metabolic as educational reference, which is not a recommendation to use it.

02Is Tesamorelin FDA approved?+

FDA approved. The FDA has approved at least one product containing this substance for a specific medical use, which means it has been through the agency review process and carries an approved label. Approval is always for named indications in named populations, so it is not a statement that any other use has been evaluated.

03What is the half-life of Tesamorelin?+

~26-38 min, subcutaneous. A half-life is an educational pharmacology figure describing how long the body takes to clear half of a substance. It is not a schedule and does not imply one.

04How is Tesamorelin stored and handled?+

Supplied lyophilized; reconstitute with sterile water; refrigerate the finished product and protect from light. Storage conditions come from a manufacturer's own label where one exists, and a compound with no approved label has no agency-reviewed handling instructions at all.

05What vial strengths of Tesamorelin are commonly sold?+

Commonly listed vial strengths are 5, 10 mg. A vial strength is a market fact about how a product is packaged. It is not a dose, and it says nothing about how much of anything belongs in any person.

Compare Tesamorelin

Educational reference only, compiled from public sources. Not medical advice, diagnosis, treatment, or a dosing recommendation, and not a recommendation to use any compound. Many compounds listed are research materials not approved for human use. Consult a qualified professional.