Tesamorelin 5mg research vial
SwissNova Labs
Tesamorelin 5mg · 5mg
≥99% Purity · COA Included
Growth Hormone

Tesamorelin 5mg

Purity: 99%+
Size: 5mg
Grade: Research
Form: Lyophilized
SwissNova Labs · Research Grade
Growth HormoneNew

Tesamorelin 5mg

Growth hormone-releasing factor analogue — 5mg starter vial for research protocols.

Visceral fat reduction — FDA-approved mechanism showing 15–18% VAT reduction in clinical trialsGH pulse preservation — stimulates natural pulsatile GH release without suppressing the hypothalamic-pituitary axisBody composition — reduces visceral fat while preserving lean muscle massCognitive support — emerging research shows improvements in executive function and memory via IGF-1 signaling
Strength5mg
$50.00
5mg · Research use only
Compound Specifications
Purity99%+
Molecular Weight5135.8 Da
Vial Size5mg
SequenceTrans-3-hexenoic acid-Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2
Vial Supply
Duration~5 weeks supply
Week 1Week 5
Why Researchers Choose This Compound

Key Benefits

01
Visceral fat reduction

FDA-approved mechanism showing 15–18% VAT reduction in clinical trials

02
GH pulse preservation

stimulates natural pulsatile GH release without suppressing the hypothalamic-pituitary axis

03
Body composition

reduces visceral fat while preserving lean muscle mass

04
Cognitive support

emerging research shows improvements in executive function and memory via IGF-1 signaling

Mechanism of Action

Active Signaling Pathway

BioHuman Research Dossier
Human Data AvailableResearch use only — not for human consumption

Investigated Pathways

GHRH-ReceptorPituitary GH ReleaseIGF-1 AxisPeripheral Tissue

Proposed Mechanism

Tesamorelin is a stabilized analog of endogenous GHRH with a trans-3-hexenoic acid group attached to the N-terminus, which protects it from dipeptidyl peptidase IV (DPP-IV) degradation and extends its half-life to 26–38 minutes. It binds to GHRH receptors on pituitary somatotrophs, triggering cAMP-mediated GH synthesis and pulsatile release. The resulting GH elevation stimulates hepatic IGF-1 production, which mediates the lipolytic effects on visceral fat.

Research Highlights

  • FDA-approved (2010) for HIV-associated lipodystrophy — one of the most rigorously studied GHRH analogs
  • Phase III trials showed 15–18% reduction in visceral adipose tissue (VAT) over 26 weeks
  • Demonstrated improvements in cognitive function (executive function, memory) in adults with mild cognitive impairment
  • Unlike direct GH, Tesamorelin preserves the natural GH feedback loop via somatostatin — no axis suppression
Human Data AvailableEvidence Strength

Human observational or open-label study data exists. Controlled trial data may be limited. Not a treatment recommendation.

Research FocusMuscle & Performance
Muscle & Performance body system research map
Muscle & Performance

For laboratory research only

All Research Systems →
Mitochondrial Zoom Sequence1 / 6
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Organism Level

Human Body

Research begins at the whole-organism level — studying systemic metabolic markers, energy expenditure, and physiological response to peptide intervention.

For laboratory research and educational purposes only.

Human Body

For research use only — not for human consumption. No treatment claims.

Full Research Hub →
Supply Calculator

How long will one vial last?

Based on standard research protocols, here's exactly what to expect from a single 5mg vial — and when to plan your next order.

One vial lasts
5
weeks
Approximately 1 month of supply at standard protocol volumes.
Reorder around week 4 to avoid running out
Your supply timeline5mg vial
Start↑ ReorderWeek 5 — empty
1
2
3
4
5
Active supplyReorder week

Vial supply estimate is based on standard research protocol volumes. Actual duration will vary based on your specific protocol design.

Research Literature

Scientific Background

Mechanism of Action

Tesamorelin is a stabilized analog of endogenous GHRH with a trans-3-hexenoic acid group attached to the N-terminus, which protects it from dipeptidyl peptidase IV (DPP-IV) degradation and extends its half-life to 26–38 minutes. It binds to GHRH receptors on pituitary somatotrophs, triggering cAMP-mediated GH synthesis and pulsatile release. The resulting GH elevation stimulates hepatic IGF-1 production, which mediates the lipolytic effects on visceral fat.

Clinical Context

Tesamorelin has the strongest clinical evidence base of any GHRH analog, with multiple Phase III trials and FDA approval. Its visceral fat reduction effects are well-documented, and emerging research suggests cognitive benefits via IGF-1 signaling in the brain. The 10mg vial allows for extended protocols without frequent reordering.

Research Highlights

  • FDA-approved (2010) for HIV-associated lipodystrophy — one of the most rigorously studied GHRH analogs
  • Phase III trials showed 15–18% reduction in visceral adipose tissue (VAT) over 26 weeks
  • Demonstrated improvements in cognitive function (executive function, memory) in adults with mild cognitive impairment
  • Unlike direct GH, Tesamorelin preserves the natural GH feedback loop via somatostatin — no axis suppression

Storage & Reconstitution

Store lyophilized powder at -20°C. Reconstitute with sterile water or BAC water immediately before use. Recommended: add 2 mL BAC water to 10 mg vial → yields 5 mg/mL. CRITICAL: Inject immediately after reconstitution — do NOT store reconstituted solution. Do not freeze reconstituted solution.

Peer-Reviewed Research

Key Studies

2007New England Journal of Medicine

Effects of Tesamorelin on Visceral Fat and Liver Fat in HIV-Infected Patients

Falutz J et al.

Tesamorelin reduced visceral adipose tissue by 15–18% over 26 weeks — the basis for FDA approval as Egrifta.

PubMed →
2012Journal of Clinical Endocrinology & Metabolism

Tesamorelin reduces visceral fat and liver fat in HIV-infected patients

Stanley TL et al.

Tesamorelin selectively reduced visceral fat while preserving subcutaneous fat with significant IGF-1 elevation.

PubMed →
2012Journal of Alzheimer's Disease

Tesamorelin improves cognitive function in older adults with mild cognitive impairment

Baker LD et al.

Tesamorelin improved executive function and memory in adults with mild cognitive impairment via IGF-1 signaling in the brain.

PubMed →
Absorption & Distribution

Pharmacokinetics

PK Parameters
Bioavailability~70% SubQ
Peak Plasma30–60 min
Half-life~26–38 min; trans-3-hexenoic acid modification protects against DPP-IV cleavage; inject immediately after reconstitution
ClearanceProteolytic degradation; renal clearance
Volume of Distribution~0.2 L/kg
What this means

Bioavailability indicates how much of the compound reaches systemic circulation. Peak plasma is when blood levels are highest. Half-life determines dosing frequency — compounds with short half-lives require more frequent dosing to maintain therapeutic levels.

The volume of distribution reflects how widely the compound distributes into tissues. A higher Vd means the compound concentrates in tissues rather than staying in plasma.

Molecular Targets

Receptor Binding Profile

GHRH receptor (GHRHR)Full agonist

Robust pulsatile GH release from pituitary somatotrophs

Pituitary somatotrophsStimulation

15–18% visceral fat reduction via GH/IGF-1 axis — FDA-approved mechanism

IGF-1 axisIndirect activation

2–3× greater IGF-1 elevation vs Sermorelin; cognitive benefits via brain IGF-1 signaling

Safety Profile

Side Effects & Adverse Events

Common
  • Injection site reactions (25%)
  • Fluid retention
  • Joint pain
Uncommon
  • Glucose intolerance
  • Carpal tunnel syndrome symptoms
Serious
  • Glucose elevation (monitor in diabetes)
  • Elevated IGF-1 (monitor levels)
NOTE:FDA-approved (Egrifta) with well-characterized clinical safety. 10mg vial for extended protocols. Inject immediately after reconstitution.
Research Safety

Contraindications & Interactions

Absolute Contraindications
Active malignancyPregnancyPituitary tumor
Relative Contraindications
Diabetes mellitus (monitor glucose)Carpal tunnel syndrome
Drug Interactions
Glucocorticoids (blunt GH response)Insulin and antidiabeticsThyroid hormones
NOTE:FDA-approved compound. Abdominal SubQ injection is the approved route. Inject within 3 hours of reconstitution.
Stack Protocols

Synergistic Compounds

Ipamorelin

GHRH + GHRP dual-signal mechanism amplifies GH pulse for enhanced body composition effects.

Tesamorelin 1 mg + Ipamorelin 200 mcg, both SubQ, once daily.

View Compound →
AOD-9604

Tesamorelin targets visceral fat via GH/IGF-1 axis while AOD-9604 directly activates adipocyte lipolysis.

Tesamorelin 1 mg SubQ daily + AOD-9604 300 mcg SubQ fasted AM.

View Compound →
Sourcing & Testing

Transparent Global Sourcing

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Manufactured

Sourced through our manufacturing partner in China

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Independent Testing

Analytical reports available from Janoshik Analytical

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Batch Verification

Batch-specific COAs with online verification via janoshik.com

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US Fulfillment

Orders fulfilled from the United States

Testing documentation varies by product and batch. Customers may review available reports and verification information before ordering. COA task numbers and verification keys can be confirmed directly at janoshik.com/verification. For research use only — not for human consumption.
RESEARCH USE ONLY:All products are sold strictly for in vitro research and laboratory use. Not intended for human consumption, clinical use, diagnosis, treatment, or prevention of any disease or condition. By purchasing, you confirm you are a qualified researcher and will use these compounds in accordance with all applicable laws and regulations.