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peptide guide · growth · trending 65

Tesamorelin

TH9507Egrifta

Synthetic 44-amino-acid analog of growth hormone-releasing hormone (GHRH). Stimulates pituitary release of endogenous growth hormone in a pulsatile manner.

category
growth
half-life
~30 minutes (with sustained pituitary effect)
research dosing
Research literature cites 1–2 mg daily subcutaneous, typically administered before bed.
vendors stocking
0
§ 01

Research notes

Mechanism

Tesamorelin is a synthetic analog of growth hormone-releasing hormone (GHRH) stabilized against rapid enzymatic degradation. Unlike direct exogenous growth hormone, tesamorelin works upstream — it stimulates the pituitary to release GH in the body's natural pulsatile pattern, which preserves the negative-feedback loops that regulate the GH–IGF-1 axis.

This mechanism distinguishes tesamorelin from related GH-axis compounds. Direct exogenous human growth hormone (hGH) bypasses the pituitary entirely; ghrelin-receptor agonists (ipamorelin, MK-677) act on a different receptor family. Tesamorelin specifically activates GHRH receptors.

The compound is FDA-approved as Egrifta for HIV-associated lipodystrophy (visceral fat reduction). Research-protocol use outside that indication is what most vendor catalog listings target.

Research dosing

The approved Egrifta dose is 2 mg daily subcutaneous, administered before bed to align with the natural overnight GH pulse. Research-protocol literature follows the same schedule:

  • 1 mg daily as a lower-end protocol dose
  • 2 mg daily matching the FDA-approved schedule
  • Cycling is common — 12-week on / 4-week off cycles appear in research-protocol writeups

Half-life is short (~30 minutes), which is why the timing of administration matters. The pituitary response continues for several hours after the peptide itself has been cleared.

Side-effect profile

Reported side effects from clinical and research-protocol literature cluster in three categories:

  • Injection-site reactions — most-reported; generally mild
  • Joint stiffness / mild edema — class effect of GH-axis compounds; typically resolves with cycling
  • Glucose tolerance changes — modest; monitored in clinical trials

What we cover

Vendor audits for tesamorelin focus on identity confirmation and purity at scale. The compound is structurally complex (44 amino acids), and lower-quality synthesis routes produce truncated peptide fragments that show up on HPLC as secondary peaks. We weight the per-batch HPLC chromatogram heavily for tesamorelin specifically.

§ 02

What it's researched for

  • visceral fat reduction
  • GHRH analog research
  • HIV-associated lipodystrophy (FDA-approved indication)
§ 03

Public Janoshik testing record — Tesamorelin

7 tests in our mirror
Public tests indexed7
Submitters7
Median purity99.6%
Identity-flagged0 / 7

Aggregated from Janoshik's public-tests database via our local mirror. Submitters with fewer than 3 public tests are listed below the ranked leaderboard as "limited data." Identity-flagged tests are surfaced on the relevant rows; check our COA verifier to look up a specific test.

Limited data (n < 3, not ranked)

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Ascension Peptides catalog COAs

Ascension Peptides publishes batch-level COAs from MZ Biolabs (HPLC-UV-MS) for Tesamorelin. 2 batches on file; median purity 99.87%.

BatchDatePurityIdentityCOA
32-012602292026-02-0799.93%confirmedopen →
32-032504282025-09-1999.81%confirmedopen →
§ 04

Where to source it

top 3 by compositeSee all 0 vendors
§ 05

Sources

  1. [01]Effects of tesamorelin on visceral adipose tissue — JAMA
  2. [02]FDA approval label — Egrifta
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