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This article is educational and does not replace medical advice. Prescription medication requires review by a licensed clinician and, when appropriate, a valid prescription. Compounded medications are not FDA-approved, and the FDA does not verify their safety, effectiveness or quality before marketing. Treatment eligibility is an individual clinical decision.

Released: ·Last reviewed: ·Methodology v4.1

Researched By
Medical Researcher · Western University of Health Sciences
Last medically reviewed: October 15, 2026 · This page is informational and does not constitute medical advice.
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CJC-1295 / Ipamorelin: evidence, legality and safety

Quick answer
FDA status, read October 15, 2026CJC-1295 and ipamorelin: neither is on the 503A list or in Category 1. FDA’s Category 2 page lists CJC-1295 under “nominated but withdrawn”, and ipamorelin as withdrawn for 503A but still in Category 2 under 503B. Neither was on the July 2026 advisory committee agenda. What the July vote did and did not change → Sources: FDA Category 2 page · 503A category lists (May 14, 2026).

CJC-1295 and ipamorelin are frequently marketed together as a growth-hormone-releasing stack. Neither is an FDA-approved finished consumer drug, and human outcome evidence for the combined protocol is limited. The pairing is a marketing convention, not an approved regimen.

Regulatory statusNot FDA-approved as a finished consumer drug.

What does the evidence actually show?

CJC-1295 and ipamorelin are frequently marketed together as a growth-hormone-releasing stack. Neither is an FDA-approved finished consumer drug, and human outcome evidence for the combined protocol is limited. The pairing is a marketing convention, not an approved regimen.

What human clinical evidence exists?

No adequate combined-protocol outcome trials in humans.

What do the animal and laboratory studies show?

Individual components show GH release preclinically; the combination's incremental benefit is not established. We keep animal and laboratory findings clearly separated from human evidence, because preclinical results routinely fail to translate to people.

What are the known and potential risks?

Combined GH-axis stimulation, unregulated sourcing, unknown long-term safety.

No consumer dosing for research compoundsThis page does not provide dosing instructions for unapproved compounds, and we do not link to research-chemical sellers. If you are considering peptide therapy, do it through a licensed clinician who can weigh your individual risks.

The lawful pathway for any prescription peptide is a licensed clinician and a licensed pharmacy. Products labeled "for research use only" are not lawfully sold for human consumption. See how to verify a peptide provider and research peptides versus prescription therapy.

Is it banned in sport?

Both components are prohibited under anti-doping codes.

Frequently asked questions

Is CJC-1295 / Ipamorelin FDA-approved?

Not FDA-approved as a finished consumer drug.

Is there human evidence for CJC-1295 / Ipamorelin?

No adequate combined-protocol outcome trials in humans.

Is CJC-1295 / Ipamorelin legal to buy?

Many peptides in this category are sold as 'research chemicals,' which is not a lawful pathway for human use. Legitimacy depends on approval status and whether a licensed clinician and pharmacy are involved. We do not link to research-chemical sellers.

Is CJC-1295 / Ipamorelin banned in sport?

Both components are prohibited under anti-doping codes.

Sources

  1. U.S. Food and Drug Administration — enforcement actions and warnings on unapproved peptide products.
  2. World Anti-Doping Agency (WADA) Prohibited List — current edition.
  3. Peer-reviewed preclinical and (where available) clinical literature, graded for evidence quality.

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How the dates on this page work. Manufacturer self-pay prices were re-read on 15 October 2026: NovoCare’s Wegovy page and Lilly’s Zepbound savings page. Foundayo prices are carried from LillyDirect pages archived 25 September 2026, because lilly.com blocked automated reads. Figures captured from telehealth provider websites carry the date we read that provider’s page, which may be earlier; where it is, the row or a dated notice says so. We do not restamp a figure we have not re-read.