Tesamorelin
99% Purity
99% Purity
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Tesamorelin

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Premium Tesamorelin for research. FDA-approved GHRH analog (44 amino acids) for HIV-associated lipodystrophy. Selective visceral fat reduction. Third-party tested, 98% purity.

Key Research Properties:

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Lyophilized powder form
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SKU: VHL-TES-001
Purity: 98% (HPLC Verified)
Form: Lyophilized Powder
Storage: Store at -20°C
Lot Number: TES-2410-03: 5mg
For Research Use Only.
All products are sold strictly for laboratory and research purposes. Products are not intended for human use or consumption of any kind.

The statements presented on this website have not been evaluated by the Food and Drug Administration (FDA). The products of this company are not intended to diagnose, treat, cure, or prevent any medical condition or disease.

What is Tesamorelin?

Tesamorelin is an FDA-approved synthetic analog of growth hormone-releasing hormone (GHRH) consisting of 44 amino acids. It is the only GHRH analog approved for treating HIV-associated lipodystrophy and is extensively researched for its effects on visceral adipose tissue.

Tesamorelin Key Properties

  • 44-amino acid GHRH analog (GHRH 1-44)
  • FDA-approved for HIV-associated lipodystrophy (2010)
  • Selective reduction of visceral adipose tissue[1]
  • Stimulates endogenous growth hormone release
  • Half-life: 26-38 minutes (requires daily administration)

Molecular Information

Molecular Weight~5135 Da
Physical FormWhite lyophilized powder
Storage-20°C (powder); 2-8°C (reconstituted, up to 14 days)
Purity≥98% (HPLC)

Mechanism of Action

Tesamorelin binds to GHRH receptors on pituitary somatotrophs, stimulating the synthesis and pulsatile release of endogenous growth hormone, which then promotes lipolysis and reduces visceral fat accumulation[2].

GHRH Receptor Activation

Activates adenylyl cyclase pathway, increasing cAMP and stimulating GH gene transcription and secretion

Visceral Fat Reduction

GH-mediated lipolysis selectively reduces visceral adipose tissue, with less effect on subcutaneous fat[3]

Downstream Effects

  • GH Release: Stimulates pulsatile GH secretion maintaining physiological patterns
  • IGF-1 Production: Secondary elevation of IGF-1 from hepatic production
  • Lipolysis: Enhanced fatty acid mobilization from visceral adipocytes
  • Metabolic Effects: Improvements in lipid profile and insulin sensitivity

Research Applications

Tesamorelin is primarily studied in contexts of visceral adiposity, metabolic dysfunction, and HIV-associated lipodystrophy[4].

Primary Research Areas

HIV-Associated Lipodystrophy

FDA-approved indication. Clinical trials demonstrate significant reduction in excess visceral fat associated with antiretroviral therapy[5].

Metabolic Syndrome

Research investigates effects on visceral obesity, triglycerides, and cardiovascular risk factors in non-HIV populations.

Clinical Evidence

  • Visceral Fat Reduction: 15-18% reduction in VAT after 26 weeks in pivotal trials[1]
  • Cardiovascular Risk: Improvements in triglycerides, waist circumference, and waist-to-hip ratio
  • Body Composition: Selective visceral fat loss with preservation of lean mass
  • Cognitive Function: Emerging research in mild cognitive impairment and Alzheimer's disease[6]
  • Liver Health: Studies examining effects on hepatic steatosis (NAFLD)

Dosing Information

For Research Use Only

Not intended for human consumption outside of approved medical use under physician supervision.

Clinical Dosing Protocols

Approved Dosing: 2 mg subcutaneously once daily

Administration Timing: Typically administered before bedtime

Reconstitution: Reconstituted with sterile water for injection

Duration: Continuous daily administration required for sustained effects; benefits diminish after discontinuation

Reconstitution

Product AmountSterile WaterConcentration
2 mg2.2 mL~0.9 mg/mL

Storage

  • Lyophilized: -20°C, protected from light
  • Reconstituted: 2-8°C for up to 14 days
  • Handling: Use sterile technique; do not shake

Safety & Side Effects

Tesamorelin has been evaluated in large-scale clinical trials with generally favorable safety profile[7].

Common Adverse Effects

  • Injection site reactions (most common: erythema, pruritus, pain)
  • Arthralgia (joint pain)
  • Peripheral edema
  • Myalgia (muscle pain)
  • Paresthesia
  • Carpal tunnel syndrome (rare, related to fluid retention)

Metabolic Considerations

Glucose Metabolism: Modest increases in HbA1c observed in some patients. Requires glucose monitoring in diabetes[8].

IGF-1 Elevation: Sustained increases in IGF-1 levels; monitoring recommended

Contraindications

  • Active malignancy or history of malignancy
  • Disruption of the hypothalamic-pituitary axis
  • Pregnancy and lactation
  • Hypersensitivity to tesamorelin or excipients

Frequently Asked Questions

Tesamorelin is FDA-approved specifically for HIV-associated lipodystrophy, has extensive Phase 3 clinical trial data in over 800 patients, and demonstrates selective visceral fat reduction with minimal effect on glucose metabolism compared to direct GH administration. Unlike CJC-1295 (which has extended half-life via DAC), tesamorelin requires daily administration but offers established safety data and regulatory approval.

Visceral adipocytes have higher density of GH receptors and are more sensitive to GH-mediated lipolysis compared to subcutaneous fat. The physiological GH elevation induced by tesamorelin preferentially mobilizes visceral fat stores, resulting in reductions in trunk fat and waist circumference while having less effect on subcutaneous adipose depots.

Clinical trials show that visceral fat gradually returns after tesamorelin discontinuation. Studies indicate that approximately 50% of the visceral fat reduction is regained within 6 months of stopping treatment, highlighting the need for continuous administration to maintain benefits. This suggests tesamorelin addresses the symptoms rather than underlying causes of visceral fat accumulation.

Clinical Trials & Research Studies

Tesamorelin has undergone extensive clinical evaluation, including two landmark Phase 3 trials published in major medical journals.

Phase 3 Studies: NEJM Publication

Design: Two identical randomized, double-blind, placebo-controlled trials

Population: N=806 HIV-infected patients with excess visceral adipose tissue

Intervention: Tesamorelin 2 mg SC daily vs. placebo for 26 weeks

Key Results:

  • Visceral adipose tissue reduction: -15.2% (tesamorelin) vs +5.4% (placebo), p<0.001
  • Trunk fat reduction: mean -1.5 kg vs +0.3 kg placebo
  • Triglyceride reduction: -29 mg/dL vs +6 mg/dL placebo
  • Improved waist circumference and waist-to-hip ratio
  • Well-tolerated; most AEs were mild injection site reactions

Reference: Falutz J, et al. N Engl J Med. 2010;363(26):2542-2552.

Cognitive Function Study

Objective: Evaluate tesamorelin effects on cognition in mild cognitive impairment

Population: Adults aged 55-87 with mild cognitive impairment

Findings: Improvements in executive function and working memory; increases in hippocampal glucose metabolism on PET scans[6]

References & Citations

  1. Falutz J, et al. "Effects of tesamorelin on body composition and metabolic parameters in HIV-infected patients with excess abdominal fat." N Engl J Med. 2010;363(26):2542-2552.
  2. Stanley TL, et al. "Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation." J Clin Endocrinol Metab. 2014;99(11):4192-4200.
  3. Grinspoon SK, Falutz J, et al. "Impact of tesamorelin on dyslipidemia, insulin sensitivity, and quality of life in HIV patients." Lancet. 2010;375(9709):123-131.
  4. Erlandson KM, et al. "Tesamorelin in HIV-associated lipodystrophy." J Acquir Immune Defic Syndr. 2016.
  5. Falutz J, et al. "Long-term safety and effects of tesamorelin on body composition." AIDS. 2010;24(9):1309-1318.
  6. Baker LD, et al. "Effects of growth hormone-releasing hormone on cognitive function in adults with mild cognitive impairment and healthy older adults." Ann Neurol. 2012;71(2):201-209.
  7. Egrifta (tesamorelin) Prescribing Information. Theratechnologies Inc. 2020.
  8. Falutz J. "Tesamorelin: a new therapy for HIV-associated lipodystrophy." Expert Opin Pharmacother. 2011;12(13):2101-2111.

3rd Party Testing & Quality Assurance

All tesamorelin batches undergo comprehensive analytical testing:

Quality Specifications

ParameterSpecificationMethod
Purity (HPLC)≥98.0%RP-HPLC
IdentityConforms to standardMS (MW ~5135 Da)
Peptide Content≥95%Amino acid analysis
Endotoxins≤5.0 EU/mgLAL assay
SterilityMeets USP standardsUSP <71>

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