Compound comparison
Ipamorelin vs Sermorelin
This page sets Ipamorelin and Sermorelin side by side using the data recorded on Peptide Science Daily: drug class, mechanism of action, regulatory status by region, the evidence grade assigned here, and the number of clinical trials tracked. It is a neutral, factual comparison and does not rank either compound or recommend one over the other.
Side-by-side comparison
- Class
- IpamorelinGrowth hormone secretagogue; ghrelin (GHS-R1a) receptor agonist (pentapeptide)SermorelinSynthetic analogue of growth hormone-releasing hormone comprising its first 29 amino acids (GHRH 1-29); formerly FDA-approved (Geref), later withdrawn from the US market
- Mechanism
- IpamorelinIn plain terms it acts like the hunger hormone ghrelin to switch on growth-hormone release.SermorelinIn plain terms, sermorelin prompts the pituitary gland to release growth hormone.
- United States (FDA)
- IpamorelinNot approved for any indication. FDA removed ipamorelin acetate from Category 2 of the interim 503A bulks list (September 2024) after the nomination was withdrawn and did not add it to the compoundable 503A list; PCAC review did not support inclusion.SermorelinPreviously approved as Geref (sermorelin acetate) for the diagnosis and treatment of growth hormone deficiency; the product was discontinued and withdrawn from the US market around 2008 for commercial reasons, not because of safety or efficacy concerns. No FDA-approved sermorelin product is currently marketed; it is available in the US only through pharmacy compounding.
- European Union (EMA)
- IpamorelinNo EMA marketing authorization; not an approved medicine in the EU.SermorelinNo current EMA marketing authorisation; not an approved medicine in the European Union.
- Australia (TGA)
- IpamorelinNot on the ARTG; an unapproved growth hormone secretagogue. Supply for human therapeutic use is restricted (prescription-only class) with no approved indication.SermorelinNot registered on the Australian Register of Therapeutic Goods (ARTG); no approved sermorelin product. Supply for human therapeutic use would be prescription-only or via compounding.
- WADA
- IpamorelinProhibited at all times under Section S2; growth hormone secretagogues including ipamorelin are explicitly listed.SermorelinProhibited at all times under Section S2 (Peptide Hormones, Growth Factors, Related Substances and Mimetics); growth-hormone-releasing factors, including GHRH and its analogues such as sermorelin, are prohibited.
- Evidence grade
- IpamorelinCSermorelinC
- Tracked clinical trials
- Ipamorelin2Sermorelin35
- Full profile
- IpamorelinSermorelin
| Attribute | Ipamorelin | Sermorelin |
|---|---|---|
| Class | Growth hormone secretagogue; ghrelin (GHS-R1a) receptor agonist (pentapeptide) | Synthetic analogue of growth hormone-releasing hormone comprising its first 29 amino acids (GHRH 1-29); formerly FDA-approved (Geref), later withdrawn from the US market |
| Mechanism | In plain terms it acts like the hunger hormone ghrelin to switch on growth-hormone release. | In plain terms, sermorelin prompts the pituitary gland to release growth hormone. |
| United States (FDA) | Not approved for any indication. FDA removed ipamorelin acetate from Category 2 of the interim 503A bulks list (September 2024) after the nomination was withdrawn and did not add it to the compoundable 503A list; PCAC review did not support inclusion. | Previously approved as Geref (sermorelin acetate) for the diagnosis and treatment of growth hormone deficiency; the product was discontinued and withdrawn from the US market around 2008 for commercial reasons, not because of safety or efficacy concerns. No FDA-approved sermorelin product is currently marketed; it is available in the US only through pharmacy compounding. |
| European Union (EMA) | No EMA marketing authorization; not an approved medicine in the EU. | No current EMA marketing authorisation; not an approved medicine in the European Union. |
| Australia (TGA) | Not on the ARTG; an unapproved growth hormone secretagogue. Supply for human therapeutic use is restricted (prescription-only class) with no approved indication. | Not registered on the Australian Register of Therapeutic Goods (ARTG); no approved sermorelin product. Supply for human therapeutic use would be prescription-only or via compounding. |
| WADA | Prohibited at all times under Section S2; growth hormone secretagogues including ipamorelin are explicitly listed. | Prohibited at all times under Section S2 (Peptide Hormones, Growth Factors, Related Substances and Mimetics); growth-hormone-releasing factors, including GHRH and its analogues such as sermorelin, are prohibited. |
| Evidence grade | C | C |
| Tracked clinical trials | 2 | 35 |
| Full profile | Ipamorelin profile | Sermorelin profile |
Common questions
- What is the difference between Ipamorelin and Sermorelin?
- Ipamorelin is classified as: Growth hormone secretagogue; ghrelin (GHS-R1a) receptor agonist (pentapeptide). Sermorelin is classified as: Synthetic analogue of growth hormone-releasing hormone comprising its first 29 amino acids (GHRH 1-29); formerly FDA-approved (Geref), later withdrawn from the US market. Ipamorelin is not approved for medical use and is prohibited in one or more regulatory or anti-doping frameworks. Sermorelin does not have a settled approval status and is not an approved medicine for general clinical use.
- Is Ipamorelin or Sermorelin approved?
- Ipamorelin is not approved for medical use and is prohibited in one or more regulatory or anti-doping frameworks. Sermorelin does not have a settled approval status and is not an approved medicine for general clinical use. Regulatory status by region is set out in the table above.
- How much clinical trial evidence is tracked for Ipamorelin and Sermorelin?
- Peptide Science Daily tracks 2 registered clinical trials for Ipamorelin (evidence grade C) and 35 for Sermorelin (evidence grade C).