Compounds
In short
Reading the whole page takes about 3 minutes.
- We sort each compound by how well it was tested, and by what the law allows.
- Approved medicines went through large trials. A regulator checked them before they were sold.
- Some are still being tested in large trials. They are not approved yet.
- The rest had little or no testing in people. What they do in people is not well known.
Why are the compounds in groups?
| Approved medicine | In clinical development | Experimental | |
|---|---|---|---|
| Tested in trials in people? | Yes In large trials, for example semaglutide and tirzepatide.1,2 | Yes In registered trials. Some are large, for example for retatrutide.3 | No Little or no formal testing in people. For BPC-157, TB-500 and KPV, most research is in cells and animals.4,5,6 |
| Benefits and risks weighed by a regulator? | Yes Before it was approved.1,2 | No Not yet. Retatrutide, for example, was not on the EU review list in October 2026.7 | No No.4,8 |
| Can a Dutch doctor prescribe it? | Yes Yes, and a pharmacy supplies it.9 | No Not in the normal way. Usually it is only available inside a trial.10,11 | No Not in the normal way.10 |
So each page works differently. For an approved medicine, it reports what the label and the trials show. For the others, it reports what was studied, in which animals or people, and what is still unknown. Medicines approved only outside the EU, for example in the US, or only by some countries’ own regulators, are in the approved group too. Their page says where, because a Dutch doctor cannot simply prescribe them.10 Products that are not peptides are listed under “Other”.
An approved name does not make every product with that name approved. A vial sold online as “research semaglutide” is not the approved medicine.12 See product risk.
How to read the evidence profile
What does the evidence profile on each card show?
| Part of the profile | The question it answers |
|---|---|
| Human clinical evidence | How far has it been tested in people? |
| Preclinical volume | How much lab and animal research exists? |
| Source independence | How many separate research groups produced it? |
| Safety characterisation | How well do we know the harms in people? |
The parts are kept apart on purpose. Many animal studies from one lab are not the same as one good trial in people. See how we grade evidence, and the Croatian lab for an example.
Authorised medicines
- PT-141
PT-141 is bremelanotide. In the US it is a prescription medicine called Vyleesi.
- Human clinical evidence
- Authorised by a regulator
- Preclinical volume
- Minimal
- Source independence
- A few groups
- Safety characterisation
- Partial
- Semaglutide
Semaglutide is an authorised EU medicine. Ozempic and Rybelsus treat type 2 diabetes. Wegovy helps manage weight.
- Human clinical evidence
- Authorised by a regulator
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Well characterised
- Tesamorelin
Tesamorelin is a lab-made version of a brain hormone. It makes the body release more growth hormone.
- Human clinical evidence
- Authorised by a regulator
- Preclinical volume
- Minimal
- Source independence
- A few groups
- Safety characterisation
- Partial
- Tirzepatide
Tirzepatide is an approved EU medicine called Mounjaro. It treats type 2 diabetes and helps manage weight.
- Human clinical evidence
- Authorised by a regulator
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Well characterised
- SS-31
SS-31 is a lab-made chain of four amino acids. Its medicine name is elamipretide.
- Human clinical evidence
- Authorised by a regulator
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Partial
- Thymosin alpha-1
Thymosin alpha-1 is a natural peptide made of 28 amino acids. It was first found in the thymus.
- Human clinical evidence
- Authorised by a regulator
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Partial
In clinical development
- Retatrutide
Retatrutide is a new drug still in testing. No country has approved it as a medicine yet.
- Human clinical evidence
- Phase III (large controlled trials)
- Preclinical volume
- Moderate
- Source independence
- A few groups
- Safety characterisation
- Partial
Experimental — not authorised in the EU, the UK or the US
- BPC-157
BPC-157 is a lab-made chain of 15 amino acids. No country has approved it as a medicine.
- Human clinical evidence
- Case reports only
- Preclinical volume
- Extensive
- Source independence
- One group dominates
- Safety characterisation
- Uncharacterised
- CJC-1295
CJC-1295 is a lab-made peptide. It makes the body release more growth hormone for days.
- Human clinical evidence
- Phase I (safety, small)
- Preclinical volume
- Minimal
- Source independence
- One group dominates
- Safety characterisation
- Partial
- Ipamorelin
Ipamorelin is a lab-made peptide. It is not an approved medicine in Europe or the US.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Moderate
- Source independence
- A few groups
- Safety characterisation
- Partial
- KPV
KPV is a lab-made chain of three amino acids. It is the tail end of the hormone alpha-MSH.
- Human clinical evidence
- None published
- Preclinical volume
- Moderate
- Source independence
- A few groups
- Safety characterisation
- Uncharacterised
- Melanotan II
Melanotan II is lab-made. It copies a hormone that darkens skin. No country has approved it.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Partial
- TB-500
TB-500 is a lab-made piece of a natural protein, thymosin beta-4. It is not an approved medicine.
- Human clinical evidence
- Case reports only
- Preclinical volume
- Moderate
- Source independence
- A few groups
- Safety characterisation
- Uncharacterised
- AOD-9604
AOD-9604 is a lab-made copy of the last part of growth hormone. It is not an approved medicine.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Minimal
- Source independence
- One group dominates
- Safety characterisation
- Partial
- Epitalon
Epitalon is a lab-made chain of four amino acids. No country is known to have approved it.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Extensive
- Source independence
- One group dominates
- Safety characterisation
- Uncharacterised
- GHK-Cu
GHK-Cu is a tiny peptide of three amino acids holding copper. It occurs in human blood.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Uncharacterised
- Hexarelin
Hexarelin is a lab-made chain of six amino acids. It makes the body release growth hormone.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Extensive
- Source independence
- A few groups
- Safety characterisation
- Partial
- MOTS-c
MOTS-c is a small peptide made inside our cells. It is not an approved medicine.
- Human clinical evidence
- None published
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Uncharacterised
- Selank
Selank is a lab-made chain of seven amino acids. It is a medicine in Russia.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Moderate
- Source independence
- A few groups
- Safety characterisation
- Uncharacterised
- Semax
Semax is a lab-made chain of seven amino acids. It is a medicine in Russia.
- Human clinical evidence
- Phase II (dose and early effect)
- Preclinical volume
- Extensive
- Source independence
- A few groups
- Safety characterisation
- Uncharacterised
Other
- NAD+ precursors
These are not peptides. NR and NMN are forms of vitamin B3 that the body turns into NAD+.
- Human clinical evidence
- Phase III (large controlled trials)
- Preclinical volume
- Extensive
- Source independence
- Broadly replicated
- Safety characterisation
- Partial
Sources
Every claim on this page links to one of these sources. Scholarly sources link to their DOI; regulatory sources to the regulator's own page.
- (2026). Wegovy (semaglutide): EPAR — overview and product information. Official product information ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
- (2026). Mounjaro (tirzepatide): EPAR — overview and product information. Official product information ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
- (2026). Retatrutide, a Triple Hormone Receptor Agonist, for Treatment of Obesity. New England Journal of Medicine. Clinical trial doi:10.1056/NEJMoa2604169 (opens an external site) ↩
- (2026). FDA Briefing Document for BPC-157-Related Bulk Drug Substances (BPC-157 (free base) and BPC-157 acetate), Pharmacy Compounding Advisory Committee meeting, 23–24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
- (2026). FDA Briefing Document for TB-500-Related Bulk Drug Substances (TB-500 (free base) and TB-500 acetate), Pharmacy Compounding Advisory Committee meeting, 23–24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
- (2026). FDA Briefing Document for KPV-Related Bulk Drug Substances (KPV (free base) and KPV acetate), Pharmacy Compounding Advisory Committee meeting, 23-24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
- (2026). Applications for new human medicines under evaluation by the CHMP — October 2026 (EMA/222468/2026). Regulator ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
- (2026). Medicines (search of centrally authorised medicines and EPARs). Regulator ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
- (2007). Geneesmiddelenwet, artikel 61 (wie UR-geneesmiddelen mag afleveren; geen aflevering zonder recept). wetten.overheid.nl (BWBR0021505), version in force from 9 September 2025. Law wetten.overheid.nl (opens an external site) — accessed 22 October 2026 ↩
- (2007). Geneesmiddelenwet, artikel 40 (verbod op geneesmiddelen zonder handelsvergunning, en de uitzonderingen). wetten.overheid.nl (BWBR0021505), version in force from 9 September 2025. Law wetten.overheid.nl (opens an external site) — accessed 22 October 2026 ↩
- (2026). Overzicht van goedgekeurde compassionate use programma's. Regulator cbg-meb.nl (opens an external site) — accessed 20 October 2026 ↩
- (2026). Standpunt: Gebruik diabetes- en afslankmedicijnen alleen zoals ze bedoeld zijn. Regulator cbg-meb.nl (opens an external site) — accessed 20 October 2026 ↩