20mg

Tesamorelin (Tesa)

20mg

121.00$

Tesamorelin is researched for its ability to stimulate growth-hormone-related signaling pathways. Studies often explore its connection to body composition signaling, tissue maintenance pathways, and metabolic regulation in laboratory models.

Tesamorelin (Tesa)

Product Name: Tesamorelin (Tesa)
Type: Growth Hormone Pathway Research Peptide

 

Research Focus:

Tesamorelin is a synthetic 44-amino-acid peptide analog of Growth Hormone-Releasing Hormone (GHRH)[1]. It stimulates endogenous growth hormone release and raises IGF-1 levels, leading to enhanced lipolysis and metabolic benefits[2]. Tesamorelin is FDA-approved for reducing visceral adipose tissue in HIV-associated lipodystrophy and is studied for metabolic disorders and aging research[3][4].

 

Research Interest:

  • Body fat and metabolism signaling studies

  • Tissue maintenance and repair signaling models

  • Hormone-regulated energy balance research

  • Age-related metabolic pathway exploration

 

Scientific Interest:

  • Growth hormone release mechanisms

  • Endocrine influence on metabolic processes

  • Cellular growth and maintenance signaling


Reconstitution:

  • Reconstitute: Add 3.0 mLbacteriostatic water per 20 mg vial → ~6.67 mg/mL concentration.

  • Standard daily dose: 2 mg (2000 mcg) once daily subcutaneously (FDA-approved protocol).

  • Easy measuring: At 6.67 mg/mL, 1 unit = 0.01 mL ≈ 66.7 mcg on a U-100 insulin syringe.

  • Storage: Lyophilized & Reconstituted: refrigerate at 2–8 °C (35.6–46.4 °F)

 

Cycle:


Standard FDA-Approved Protocol (3.0 mL = ~6.67 mg/mL)

WEEK

DAILY DOSE (MG / MCG)

UNITS (PER INJECTION) (ML)

Week 1

1 mg / 1000 mcg

15 units (0.15 mL)

Weeks 2–12+

2 mg / 2000 mcg

30 units (0.30 mL)


Frequency:
Inject once dailysubcutaneously, preferably in the evening to coincide with nocturnal GH release[5][6]. The 2 mg daily dose is the standard FDA-approved regimen for HIV lipodystrophy[7][8]. A one-week titration at 1 mg may improve tolerability before advancing to the full 2 mg dose.

Reconstitution Steps

  1. Draw 3.0 mL bacteriostatic water with a sterile syringe.

  2. Inject slowly down the vial wall; avoid foaming.

  3. Gently swirl until dissolved (do not shake).

  4. Label and refrigerate at 2–8 °C (35.6–46.4 °F), protected from light.

IMPORTANT NOTICE:

This product is intended strictly for laboratory research. It is not intended to diagnose, treat, cure, or prevent any disease.

King St. West,
Toronto, Ontario
Canada.

M6K 3M3