Peptide Stack for Muscle Growth: Evidence, Doses and Units

The four combinations sold for muscle growth: who claims what, how many human trials exist for each component, the reported doses, and the units per draw.

Medibact Guides · Published 2026-09-18

Illustration: Three clear glass vials on a white lab bench, one with pale blue powder, and a metal spatula.
Illustration

This page reports the peptide combinations sold for muscle growth: what each component is, who claims what, what the human evidence holds when it is counted, the reported doses with their sources, and how the vials are reconstituted and drawn. It ranks nothing and presents no protocol; every figure carries its source and the date it was read.

A stack is two or more compounds used over the same period. The combinations sold for muscle growth are built from growth-hormone-axis peptides: CJC-1295, tesamorelin and sermorelin are analogues of growth-hormone-releasing hormone, the signal that tells the pituitary to release growth hormone; ipamorelin is a growth-hormone secretagogue acting on the ghrelin receptor, a second route to the same release; IGF-1 LR3 is an analogue of insulin-like growth factor 1, the hormone the liver makes in response to growth hormone, modified to bind less to its carrier proteins. Four combinations recur: CJC-1295 with ipamorelin, tesamorelin with ipamorelin, sermorelin alone or with ipamorelin, and IGF-1 LR3 added to any of them.

The combinations, and who promotes them

The phrase "best peptide stack for muscle growth" is answered on the first page of results by telehealth clinics, med-spa blogs, a peptide-education site and a video titled as the best stack for building muscle (read 2026-09-18). Their claims, in their own terms: CJC-1295 with ipamorelin "raises the body's own growth hormone" and pairs a long-acting baseline with a "clean, selective pulse"; tesamorelin with ipamorelin is framed as the fat-loss variant, with tesamorelin credited as having "the strongest human evidence" because it has a label; sermorelin is presented as the milder or older option; IGF-1 LR3 as the compound that acts "downstream". None cites a trial of the combination it describes; there is none. The site's own CJC-1295 with ipamorelin article and tesamorelin with ipamorelin article cover those two pairings; the sermorelin and ipamorelin page covers the third.

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What the human evidence holds, counted

Component Approved label ClinicalTrials.gov registrations (2026-09-18) PubMed papers under the trial filter Who was studied, and for what
CJC-1295 none (DailyMed: zero records) 1 (NCT00267527, terminated) 2 (both 2006, DAC form) healthy adults; GH and IGF-I over weeks
Ipamorelin none 3 (two completed Helsinn trials; one unrelated multi-intervention study) 2 (1999 pharmacokinetics; 2014 postoperative ileus) healthy men and bowel-surgery patients; intravenous
CJC-1295 with ipamorelin none 0 0 (10 papers mention both, all reviews or analytical chemistry) nobody
Tesamorelin EGRIFTA WR, EGRIFTA SV 24 23 HIV-infected adults; visceral fat
Tesamorelin with ipamorelin none 0 none nobody
Sermorelin GEREF, withdrawn 2009 (not for safety or effectiveness) 27 0 under a title-and-abstract trial filter; 17 human-tagged records children with growth hormone deficiency; diagnostic tests; a terminated study in older adults
Sermorelin with ipamorelin none 0 0 (5 papers mention both, all reviews) nobody
IGF-1 LR3 none 0 0 (84 records) cell culture and livestock

The CJC-1295 record is two 2006 papers on the DAC form in healthy adults: GH up 2- to 10-fold for 6 days or more and IGF-I up 1.5- to 3-fold for 9 to 11 days after single doses, a half-life of 5.8 to 8.1 days, and tolerability described as best at 30 or 60 mcg/kg (Teichman et al., PMID 16352683; Ionescu and Frohman, PMID 17018654). The ipamorelin record is intravenous: 4.21 to 140.45 nmol/kg over 15 minutes in healthy men, 3 to 100 mcg/kg at a molecular weight of 711.9 (Gobburu et al. 1999, PMID 10496658), and 0.03 mg/kg twice daily after bowel resection with no significant difference from placebo (Beck et al. 2014, PMID 25331030). Tesamorelin's pivotal trial is in the facts above (Falutz et al. 2010, PMID 20101189); sermorelin's labelled use was paediatric (Prakash and Goa 1999, PMID 18031173); IGF-1 LR3 has no human study, which Peptifact's IGF-1 LR3 dosage page also found after reading all 44 records of a narrower search.

Reported doses, with sources

Component Kind of source Figure Date read
CJC-1295 with DAC trial protocol 30, 60 or 90 mcg/kg, single subcutaneous doses; 2.1, 4.2 or 6.3 mg at 70 kg papers 2006; read 2026-09-18
CJC-1295 with DAC vendor and protocol pages 1 to 2 mg once weekly, or 1 mg twice weekly 2026-09-18
CJC-1295 without DAC protocol pages 100 to 300 mcg per injection, one to three times a day 2026-09-18
Ipamorelin trial protocols 3 to 100 mcg/kg intravenously over 15 minutes; 0.03 to 0.06 mg/kg intravenously two or three times daily papers 1999 and 2014; registry 2026-09-18
Ipamorelin clinic and protocol pages 100 to 300 mcg under the skin, one to three times a day 2026-09-18
Tesamorelin approved label 1.28 mg once daily (EGRIFTA WR); 1.4 mg once daily (EGRIFTA SV) labels 3/2025 and 2/2024; read 2026-09-18
Tesamorelin trial protocol 2 mg daily for 26 weeks Falutz 2010
Sermorelin former label (paediatric) 30 mcg/kg once daily at bedtime Prakash and Goa 1999; Federal Register 2013
Sermorelin compounding and clinic pages 200 to 300 mcg at night 2026-09-18
IGF-1 LR3 protocol pages 20 to 80 mcg a day 2026-09-18
Mecasermin (INCRELEX), the nearest labelled IGF-1 approved label 0.04 to 0.08 mg/kg twice daily, maximum 0.12 mg/kg, within 20 minutes of a meal label 7/2025; read 2026-09-18

The INCRELEX row is there for scale, not as a proxy: it is native IGF-1 in children with severe primary IGF-1 deficiency, dosed by weight and tied to meals because of hypoglycaemia, and none of that transfers to an analogue with no human data.

Reconstitution and the units per draw

Concentration is the milligrams in the vial divided by the millilitres of water; the draw on a U-100 syringe is the quantity in mg divided by that concentration, times 100. The rows use the vial sizes the site's calculators carry.

Vial Water Concentration Quantity Units (U-100)
CJC-1295 and ipamorelin blend, 10 mg (5 mg and 5 mg) 2 mL 5 mg/mL blend; 2.5 mg/mL each 100 mcg of each 4 units
Tesamorelin 10 mg 2 mL 5 mg/mL 2 mg 40 units
same vial 2 mL 5 mg/mL 1.28 mg 25.6 units
Tesamorelin 5 mg 1 mL 5 mg/mL 1.4 mg 28 units
Ipamorelin 5 mg 2 mL 2.5 mg/mL 200 mcg 8 units
Sermorelin 5 mg 2 mL 2.5 mg/mL 300 mcg 12 units
IGF-1 LR3 1 mg 1 mL 1 mg/mL 50 mcg 5 units
IGF-1 LR3 1 mg 2 mL 0.5 mg/mL 50 mcg 10 units

A blend vial fixes the ratio of its two peptides at fill time, so a single draw delivers both in whatever proportion the vial holds; separate vials allow independent amounts but mean two draws and two calculations. The blend calculator does the per-component arithmetic for either case, and the single-compound calculators cover each vial: CJC-1295 with ipamorelin, CJC-1295, ipamorelin, tesamorelin, sermorelin and IGF-1 LR3. The scales and barrels are on the insulin syringe units page.

What the figures omit

The trial figures omit the stack: every human number above was measured for one compound, in a population not training for muscle, on an endpoint that was not muscle. The label figures omit the purpose: tesamorelin's label is for HIV-associated abdominal fat and sermorelin's withdrawn label was for children. The circulating figures omit their origin and change the molecule without saying so: the CJC-1295 in the blends is the no-DAC form, never given to a person in a published study, while the 2006 trials used the DAC form at milligram doses. Route, frequency, duration and population therefore belong to a handful of papers and two labels, not to the combinations.

Status

The component guides on the store cover regulatory status in full: Medibact's CJC-1295 guide, ipamorelin guide, tesamorelin guide, sermorelin guide and IGF-1 LR3 guide. In September 2023 FDA placed CJC-1295, ipamorelin acetate and AOD-9604 in Category 2 of its interim 503A bulks list, the category for substances identified as presenting significant safety risks (Alliance for Pharmacy Compounding update, 2023-09-29); an FDA Law Blog post of 2026-04-21 reports FDA moving peptides scheduled for advisory review out of Category 2 in 2026. FDA's own list pages refused this site's requests on 2026-09-18, so their current text is not quoted.

The stacks hub indexes every combination page; the CJC-1295 reconstitution page works that vial in detail; the dosage pages for CJC-1295, ipamorelin, tesamorelin and sermorelin hold each compound's reported range with its source, indexed on the dosage hub; the how peptides are injected page reports the procedure as labels describe it.

This page does not recommend a stack, a dose, a schedule or a vendor. It reports what registries, trials, labels and the promoting pages state, each with its date, and it does the arithmetic on the vials.

Sources and dates

Opened 2026-09-18: the ClinicalTrials.gov v2 API for each component and each pairing, with the records NCT00267527, NCT00672074 and NCT01280344; the DailyMed SPL search API for each component and the EGRIFTA WR, EGRIFTA SV and INCRELEX labels; PubMed through the NCBI E-utilities with the trial-type filter, and the abstracts of PMID 16352683, 17018654, 10496658, 25331030, 20101189 and 18031173; PubChem CID 9831659; the Federal Register notice of 2013-03-04 on GEREF (via GovInfo); the Alliance for Pharmacy Compounding update of 2023-09-29 and the FDA Law Blog post of 2026-04-21; telehealth, med-spa and protocol pages carrying the circulating figures. Corrections go to the contact page.

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Frequently asked questions

What is the best peptide stack for muscle growth?

No combination has been tested for muscle growth in a human trial, so no ranking rests on evidence. Counted on 2026-09-18: zero registrations for CJC-1295 with ipamorelin, tesamorelin with ipamorelin, or sermorelin with ipamorelin; two human trials of CJC-1295 (DAC form, GH and IGF-I in healthy adults); two of ipamorelin (intravenous, bowel-surgery recovery); an approved label for tesamorelin in HIV-associated abdominal fat; a withdrawn paediatric label for sermorelin; nothing in humans for IGF-1 LR3. This page reports that record and ranks nothing.

Does CJC-1295 with ipamorelin build muscle?

No human trial has asked. The two CJC-1295 trials (2006) measured GH and IGF-I in healthy adults after the DAC form and did not measure muscle; the ipamorelin trials measured bowel recovery after surgery with intravenous dosing. Ten PubMed papers mention both names and every one is a review or an analytical-chemistry paper (read 2026-09-18). The pages claiming lean-mass gains cite the GH physiology, not a trial of the pair. The site's combination article covers the pairing in detail.

Is tesamorelin better than CJC-1295 and ipamorelin for muscle?

The question has no trial behind it in either direction. Tesamorelin is the one component with a label, and the label is for excess abdominal fat in HIV-infected adults: 1.28 mg (EGRIFTA WR) or 1.4 mg (EGRIFTA SV) once daily, on a pivotal trial where 2 mg daily cut visceral fat by 10.9% against 0.6% on placebo over six months. Muscle was not the endpoint, and no head-to-head study of tesamorelin against CJC-1295 with ipamorelin exists on ClinicalTrials.gov (read 2026-09-18).

What doses are reported for the muscle-growth stack?

The trial and label figures: CJC-1295 with DAC 30 to 90 mcg/kg as single subcutaneous doses (2006); ipamorelin 0.03 to 0.06 mg/kg intravenously two or three times daily (2008 to 2013 trials); tesamorelin 1.28 or 1.4 mg daily on label and 2 mg daily in its pivotal trial; sermorelin 30 mcg/kg nightly on its former paediatric label. The circulating figures on protocol and clinic pages (read 2026-09-18): 100 to 300 mcg of CJC-1295 (no DAC) and of ipamorelin one to three times a day, 1 to 2 mg of tesamorelin, 200 to 300 mcg of sermorelin, 20 to 80 mcg of IGF-1 LR3. They are reported here, not endorsed.

How are the vials for a stack reconstituted and drawn?

Each vial is its own calculation: concentration is the milligrams in the vial divided by the millilitres of water, and the draw in U-100 units is the quantity in mg divided by that concentration, times 100. A 10 mg blend vial of CJC-1295 and ipamorelin in 2 mL is 5 mg/mL for the blend and, at a 5 mg and 5 mg split, 2.5 mg/mL of each, so 100 mcg of each is 4 units. Separate vials mean separate draws; a blend vial fixes the ratio at fill time. The site's blend calculator does the per-component arithmetic.

How many human trials test these combinations?

Zero. ClinicalTrials.gov returned no study for any of the three pairings on 2026-09-18, and PubMed's trial filter returns no paper on any combination. The components' own trial counts are small and off-topic for muscle: two CJC-1295 papers on GH and IGF-I, two ipamorelin papers on pharmacokinetics and postoperative ileus, 23 tesamorelin trial papers almost all in HIV lipodystrophy, sermorelin's paediatric and diagnostic studies, and nothing in people for IGF-1 LR3.