Peptide Blends

Tesamorelin & Ipamorelin Blend

A research blend combining tesamorelin (a stabilized GHRH analogue) with ipamorelin for synergistic GH release, combining tesamorelin's unique visceral fat research profile with ipamorelin's clean GHS selectivity.

C221H366N72O67S / C38H49N9O5Half-life: Tesamorelin: ~30-40 min; Ipamorelin: ~2 hours

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⚠ Research & Educational Use Only. Tesamorelin & Ipamorelin Blend is a research chemical documented here for scientific education. All information references peer-reviewed literature and preclinical/clinical study data. Not for human consumption. Not medical advice. Consult a licensed researcher or healthcare professional before any laboratory use.

Medically reviewed by Dr. Amanda Haslett, MBChB MRCGPWritten by the KnowYourPeptide Research TeamLast updated April 2026
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Key Takeaways
  • Synergistic GH release via GHRHR + GHS-R1a
  • Tesamorelin's documented human visceral fat reduction effect
  • Ipamorelin's clean GH selectivity (minimal cortisol/prolactin)
  • Tesamorelin & Ipamorelin Blend is not FDA-approved for human use. It is a research chemical for scientific study only.

Research At a Glance

  • Synergistic GH release via GHRHR + GHS-R1a
  • Tesamorelin's documented human visceral fat reduction effect
  • Ipamorelin's clean GH selectivity (minimal cortisol/prolactin)
  • Well-characterized human clinical data from tesamorelin component

What is Tesamorelin & Ipamorelin Blend?

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Tesamorelin & Ipamorelin Blend pairs tesamorelin, a stabilized trans-3-hexenoic acid-modified analogue (FDA approved as Egrifta for HIV lipodystrophy), with ipamorelin. The combination leverages tesamorelin's more stable GHRH-pathway activation and its documented clinical-level visceral fat reduction effect, amplified by ipamorelin's clean GHS-R1a-mediated somatostatin suppression.

What It Is

  • Tesamorelin: a modified analogue with a trans-3-hexenoic acid substitution at position 1, improving resistance to dipeptidyl peptidase IV degradation; FDA approved for HIV-associated lipodystrophy
  • Ipamorelin: selective GHS-R1a agonist with minimal off-target hormone effects
  • Combination designed to capture tesamorelin's documented clinical fat-reduction profile with amplified GH release from ipamorelin co-administration

How It Works

  • Tesamorelin activates GHRHR with slightly longer duration of action than sermorelin due to its stability modification
  • Ipamorelin suppresses hypothalamic somatostatin and independently stimulates GHS-R1a
  • Synergistic GH pulses exceed tesamorelin alone by 2-3 fold in animal models

Key Research Findings

  • Tesamorelin alone (from clinical trials): 26 week treatment reduced visceral adipose tissue by 15-18% in HIV lipodystrophy patients vs placebo; increased 100-150%
  • Combination: Limited direct combination trial data; extrapolation from component data suggests enhanced GH and vs either alone
  • Visceral fat: Tesamorelin's documented anti-adiposity effect through GH-mediated lipolysis

Dosing From the Literature

  • Tesamorelin: 1-2 mg subcutaneous daily (FDA approved dose: 2 mg/day)
  • Ipamorelin: 200-300 mcg subcutaneous, co-administered
  • Once daily administration preferred

Storage and Handling

  • Lyophilised tesamorelin: 2-8 degrees C; 24 months
  • : 2-8 degrees C; use within 21 days

Key Research Benefits

Documented effects observed in preclinical and clinical studies on Tesamorelin & Ipamorelin Blend. See all Peptide Blends peptides for comparison.

Synergistic GH release via GHRHR + GHS-R1a
Tesamorelin's documented human visceral fat reduction effect
Ipamorelin's clean GH selectivity (minimal cortisol/prolactin)
Well-characterized human clinical data from tesamorelin component

Side Effects & Risks

Adverse effects reported in the research literature. All data sourced from preclinical and clinical study reports. View all peptides' side effects →

Dosing Data from the Literature

Doses referenced below are sourced from published preclinical and clinical studies. Use the peptide dose calculator to convert these values to injection volume.

Research Dosing Protocol

Tesamorelin 1-2 mg + ipamorelin 200-300 mcg per administration. Once daily.

Enter your vial size and target dose to get the exact injection volume.

Administration in Research Settings

Standard reconstitution and administration methodology for laboratory research use.

. Tesamorelin should be administered once daily for sustained clinical-level GH stimulation.

Explore Further

Quick Reference

Half-Life
Tesamorelin: ~30-40 min; Ipamorelin: ~2 hours
Formula
C221H366N72O67S / C38H49N9O5
Legal Status
Tesamorelin is FDA approved for HIV-associated lipodystrophy; ipamorelin is a research chemical. Combined blend is research only.
Storage
Lyophilised: 2-8 degrees C. Reconstituted: 2-8 degrees C; use within 21 days.

Research Use Only

This information is for educational research purposes only. This is not medical advice. Consult a qualified healthcare professional.

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