Home / Learn / CJC-1295 and Ipamorelin: dosing in the published literature
Research digest

CJC-1295 and Ipamorelin: dosing in the published literature

Last updated: 11 September 2026

This page reports what published studies actually administered, not what anyone should take. The two compounds have very different evidence behind them: CJC-1295 has been through placebo-controlled human trials with published dose ranges, while ipamorelin’s published work is almost entirely preclinical. The combination the two are sold in has never been tested in a human trial at all — a gap worth knowing before reading any dosing chart elsewhere.

CJC-1295: what the human trials used

The principal human dataset is Teichman et al. (2006), published in the Journal of Clinical Endocrinology & Metabolism. It comprised two randomised, placebo-controlled, double-blind ascending-dose trials of 28 and 49 days in healthy adults aged 21 to 61, given CJC-1295 in ascending single doses or in multiple weekly or biweekly doses.

After a single subcutaneous injection the study reported dose-dependent increases in mean plasma GH of two- to ten-fold lasting six days or more, and increases in mean plasma IGF-I of 1.5- to three-fold lasting nine to eleven days. The estimated half-life of CJC-1295 was 5.8 to 8.1 days. The authors concluded the compound was safe and relatively well tolerated, particularly at doses of 30 or 60 µg/kg.

Two things follow. The dose is expressed per kilogram of bodyweight, so a single figure in milligrams is not what the trial tested. And the multi-day half-life is why the published schedules are weekly or biweekly rather than daily — the exposure from one injection is still present a week later.

Ipamorelin: no published human dose-ranging trial

Ipamorelin was characterised by Raun et al. (1998) in the European Journal of Endocrinology, the paper that named it the first selective growth hormone secretagogue. It is a pentapeptide identified within a series derived from growth hormone-releasing peptide-1, and the selectivity claim is that it releases GH with less effect on other pituitary hormones than the earlier GHRP compounds.

That work is preclinical. There is no published human dose-ranging trial for ipamorelin comparable to the CJC-1295 dataset, so no human dose has been established for it. Any ipamorelin dosing figure circulating online is not traceable to a human trial.

The combination has not been studied in humans

CJC-1295 and ipamorelin are almost always discussed together, and the rationale is mechanistic: a GHRH analogue raises the size of a growth hormone pulse while a secretagogue acting on the ghrelin receptor triggers one. The reasoning is sound as pharmacology. It is not the same thing as evidence.

No published human trial has administered the two compounds together and measured the result. Dose figures presented for the combination are therefore derived from the individual compounds at best, and invented at worst.

What Body Pharm states about its own pen

Separate from the literature, Body Pharm supplies CJC-1295 and ipamorelin in one pre-loaded 20 mg 3 mL pen and describes its own protocol on the product page and as the bedtime protocol on the sleep page: one dose before bed, five nights per week, on an empty stomach. That is the supplier’s stated protocol for its own product, not a finding from any of the studies above, and it is presented as such.

Every batch is third-party tested for identity, purity and sterility, and the certificate of analysis for the specific lot is reachable from the QR code on the pen.

Frequently asked questions

What dose of CJC-1295 was used in human studies?

Teichman et al. (2006) tested ascending doses and reported the compound was safe and relatively well tolerated particularly at 30 or 60 µg/kg. Doses were per kilogram of bodyweight, and the trials used weekly or biweekly schedules rather than daily.

Why are CJC-1295 schedules weekly rather than daily?

Because of the half-life. Teichman et al. estimated 5.8 to 8.1 days, with GH elevated for six days or more and IGF-I for nine to eleven days after a single injection. Exposure from one dose is still present the following week.

Is there an established ipamorelin dose?

No. Ipamorelin’s published characterisation (Raun et al., 1998) is preclinical, and no human dose-ranging trial has been published. Any specific human figure is not traceable to a trial.

Has the CJC-1295 and ipamorelin combination been trialled?

Not in a published human trial. The pairing rationale is mechanistic — one compound amplifies a growth hormone pulse and the other triggers it — but no study has administered both and measured the outcome.

Sources

This page reports dosing and adverse events as they appear in published research. It is a summary of the literature, not dosing guidance, a protocol or a recommendation, and figures from a study do not transfer to any individual. None of the compounds described here holds a marketing authorisation from the EMA. Decisions about use belong with a qualified clinician who knows your history. These statements have not been evaluated by the EMA.