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PureAmino Research
Tesa
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99%+ Purity
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Growth Hormone Peptides

Tesa

TesamorelinTH9507EgriftaGHRH Analog
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A growth hormone releasing peptide studied for GH secretagogue activity. Tesa supports the hypothalamic-pituitary axis in growth hormone research protocols.

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Compound Profile

Pharmaceutical Data Sheet

PureAmino ResearchResearch Grade Β· 99%+ Purity

Growth Hormone Peptides

Tesa

Tesamorelin

CAS Number

218949-48-5

Molecular Formula

C₂₂₁H₃₆₉N₆₅O₆₅S

Molecular Weight

5,135.77 g/mol

Purity

> 99% HPLC

Designation

RUO Β· Research Use Only

Not for human or veterinary consumption. For in vitro laboratory research only.

Tesa

Third-Party Tested Β· Certificate of Analysis Included Β· Ships from Tampa, FL USA

Batch VerifiedLyophilized
FDA
Approved Analog (Egrifta β€” HIV Lipodystrophy)
44 aa
Modified GHRH Polypeptide
~18%
Visceral Fat Reduction (Phase 3 Pooled)
806 pt
Pooled Phase 3 Trial Population

Mechanism of Action

How Tesa Works

Tesamorelin is a synthetic 44-amino acid polypeptide analog of growth hormone-releasing hormone (GHRH) with enhanced N-terminal stability. It binds GHRH receptors on anterior pituitary somatotrophs to stimulate endogenous pulsatile GH secretion and downstream IGF-1 production β€” driving lipolysis, visceral fat reduction, and improved body composition while preserving physiological GH feedback regulation.

GHRH
GHRH Receptor
Primary β€” GH Secretion
  • Binds GHRH-R on anterior pituitary somatotrophs
  • Activates Gs-cAMP-PKA signaling cascade
  • Augments both basal and pulsatile GH release
IGF
IGF-1 Axis
Downstream β€” Anabolic & Lipolytic
  • IGF-1 elevation of ~181 Β΅g/L in healthy research cohorts (P<0.0001)
  • Drives visceral adipose tissue lipolysis
  • Increases skeletal muscle area and density (Hounsfield units)
VAT
Visceral Adiposity
Clinical β€” Body Composition
  • Selective reduction of visceral adipose tissue sustained 52 weeks
  • Preserves subcutaneous adipose tissue
  • Reduces hepatic fat by ~40% relative to placebo
Key Mechanism
GHRH-R Activation β†’ Pulsatile GH Secretion β†’ IGF-1 & Lipolysis

Tesamorelin binds GHRH receptors on pituitary somatotrophs, activating Gs-cAMP-PKA signaling that stimulates GH gene transcription and pulsatile GH release. Once-daily treatment augments both basal and pulsatile GH secretion, elevating IGF-1 by ~181 Β΅g/L (P<0.0001 in research cohorts). This drives selective lipolysis in visceral adipose depots and improves muscle density.

Primary Source

Falutz J et al., J Clin Endocrinol Metab (2010): Pooled Phase 3 analysis of tesamorelin in HIV lipodystrophy.

Preclinical Findings

Research Models

GH Secretion Augmentation (Basal + Pulsatile)88%
Visceral Adiposity Reduction78%
Hepatic Steatosis Improvement72%
Body Image Score Improvement68%

Clinical Data

Pooled Phase 3: Sustained Visceral Fat Reduction Over 52 Weeks

FDA-Approved Analog β€” Phase 3 Pooled

A pooled analysis of two Phase 3 trials (n=806, 2:1 tesamorelin 2mg vs. placebo) demonstrated sustained visceral adipose tissue reduction maintained for up to 52 weeks. Exploratory analyses showed increased skeletal muscle density (1.56–4.86 Hounsfield units, all P<0.005), improved lipid profiles, ~40% relative hepatic fat reduction, and improved body image scores (belly appearance distress P=0.002).

Visceral Adipose Tissue Reduction18%
Hepatic Fat Reduction (Relative to Placebo)40%
Skeletal Muscle Density Improvement65%
Source

Falutz J et al., J Clin Endocrinol Metab (2010); Stanley TL et al., J Infect Dis (2019).

Pooled Phase 3 RCTs, n=806 (2:1 randomization); 52-week treatment

Research Outcomes

Key Research Success Metrics

18%
visceral fat reduction
Sustained over 52 weeks of treatment
Pooled Phase 3 analysis
40%
hepatic fat reduction
Relative to 27% increase in placebo arm
Stanley et al., 2019
65%
muscle density improvement
Four truncal muscle groups (P<0.005)
Exploratory secondary analysis

Safety Profile

Research Safety Notes

  • Overall well tolerated without clinically meaningful changes in glucose parameters in pooled Phase 3
  • No significant impact on diabetes control vs. placebo in 12-week T2D RCT (n=53)
  • Injection site reactions (erythema, pruritus) are the most common local AEs
  • Arthralgia and peripheral edema observed β€” consistent with GH-class elevation
  • No de novo liver enzyme elevations; some studies showed decreases in pre-existing ALT levels
Research Disclaimer

Tesa / Tesamorelin clinical data references the FDA-approved Egrifta for HIV-associated lipodystrophy. Research compound is for laboratory use only.

About Tesa

A growth hormone releasing peptide studied for GH secretagogue activity. Tesa supports the hypothalamic-pituitary axis in growth hormone research protocols.

All PureAmino Research compounds are manufactured to research-grade standards and independently tested by Janoshik Analytical & Kovera Labs. The Certificate of Analysis for this compound includes full HPLC chromatography data, mass spectrometry confirmation, net purity percentage, and net content verification.

⚠️

Research Use Only

This product is strictly for in vitro research and laboratory use only. Not for human or veterinary consumption. By purchasing, you confirm use in a controlled research setting.

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