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Growth Hormone & Secretagogues · 10mg + 3mg
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Janoshik-tested · 10 vials per kit
Tesamorelin + Ipamorelin is a research blend studied in preclinical research for dual-pathway growth hormone axis regulation. Tesamorelin acts on upstream GHRH signaling while Ipamorelin directly influences GH release at the pituitary level. Research has examined their combined potential for studying rhythmic characteristics and regulatory intensity of the growth hormone axis in metabolic and endocrine feedback models.
Blended compound — purity note
Peptide blends are not tested for combined purity as a single compound. However, every component is sourced from the same supplier as our individual peptide products, all of which carry valid Janoshik Analytical COAs. Those certificates apply equally to the same peptides in this blend. View individual COAs →
≥98%
Purity
Lyophilised
Format
2–3 wks
Arrival
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Research Use Only — Disclaimer
This product is intended solely as a research chemical for laboratory and scientific study purposes only. It is not approved by the TGA or any regulatory body for human or animal consumption, therapeutic use, or clinical application. The information provided on this website is for educational purposes only. Handling must be limited to suitably qualified professionals operating within applicable laws and regulations. This product is not classified as a drug, food, cosmetic, or medicinal product and must not be used or labelled as such. By purchasing, you confirm you are a qualified research professional and accept full responsibility for compliance with all relevant laws in your jurisdiction.
Tesamorelin
Egrifta
Tesamorelin is a synthetic analog of GHRH(1-44) modified with a trans-3-hexenoic acid group at the N-terminus for stability. This modification protects against cleavage by dipeptidyl peptidase IV (DPP-IV), extending biological half-life while preserving full GHRH receptor agonist activity. Approved by the FDA in 2010 as Egrifta for HIV-associated lipodystrophy — abdominal fat accumulation in HIV patients on antiretroviral therapy.
Tesamorelin binds GHRH receptors on anterior pituitary somatotrophs to stimulate GH release in physiological pulses, subsequently raising IGF-1 and IGFBP-3 levels. Unlike exogenous GH, pituitary-mediated release maintains feedback regulation, reducing the risk of supraphysiological IGF-1. In lipodystrophic subjects GH-mediated lipolysis preferentially targets visceral adipose tissue. Shorter-acting than CJC-1295 DAC due to lacking albumin-binding technology.
Phase 3 EGRIFTA trials documented significant visceral adipose tissue reduction (15-20% by MRI) in HIV-lipodystrophy patients. Research continues in non-HIV applications including age-related GH deficiency and Alzheimer's disease — the SNAP-NL trial demonstrated reduction in amyloid burden in older adults with mild cognitive impairment. Metabolic syndrome-associated visceral obesity is another active research area.
Key References
For research reference only. All information pertains to preclinical or published human trial data. Not intended as medical advice. This product is for research use only.
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