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Evidence: LowPeptide Clinical Trials Pipeline & In-Development

Obinepitide

also known as: TM30338, TM-30338, Obinepitida

7TM Pharma's first-in-class obesity peptide, a single molecule that switches on both the Y2 and the Y4 gut satiety receptors. Its human testing ended in the late 2000s; the only published figures are the company's own, and no results ever reached a peer-reviewed journal.

Obinepitide (TM30338) is an injectable peptide that 7TM Pharma, a Danish company, developed for obesity in the 2000s. It is a synthetic analogue that merges the actions of two hormones the gut releases during a meal: peptide YY, which curbs appetite through the Y2 receptor, and pancreatic polypeptide, which does so through the Y4 receptor. 7TM Pharma reported that a once-daily injection cut food intake for at least nine hours in a phase I/II study in adults with obesity and was well tolerated, and it began a phase II study in 2007. No trial result was ever published in a journal, the drug reached no higher than phase 2 in ChEMBL, and it is approved nowhere.

No dosing data yet Details ↓

Mechanism of action

Obinepitide is built to act like two of the body's own meal signals at once. After eating, the gut releases peptide YY, which dampens appetite mainly through the Y2 receptor, and pancreatic polypeptide, which does the same mainly through the Y4 receptor; obinepitide is a single peptide analogue that engages both receptors, which 7TM Pharma described as a first-in-class, dual Y2-Y4 agonist reaching the two receptors with similar, high potency (7TM Pharma announcement, 2006; DrugBank DB05045). Its listed structure is that of a pancreatic-polypeptide analogue (NCATS Inxight / FDA GSRS UNII 926PP306RV; formula C185H288N54O55S2). The company's stated rationale was that adding Y4 activity to the Y2 activity of peptide YY would curb appetite more fully than peptide YY alone; it reported that in diet-induced obese animals obinepitide reduced body weight over the long term more than PYY3-36, which acts only at Y2. The 2024 review carded below places it among the newer pancreatic-polypeptide-derived ligands built on this receptor system (PMID 38430725). How the mechanism behaves over months in people was never reported.

Primary uses

  • Investigational: obesity (phase I/II and phase II completed in the 2000s, company-reported, no published results; development dormant)

Typical dosing

subcutaneous, once daily in trials

No approved dose and no human dose in a peer-reviewed paper. 7TM Pharma described once-daily injection under the skin in its phase I/II study but published no amount, so none is printed here and none is inferred.

Regulatory status

Not approved anywhere: Drugs@FDA and the openFDA label endpoint hold no record for obinepitide or TM30338 (searched November 5, 2026), and ChEMBL records a highest clinical phase of 2 (CHEMBL2108338). 7TM Pharma said it completed a phase I/II study in adults with obesity in 2006 and began a phase II study in 2007, but no trial of obinepitide is registered on ClinicalTrials.gov and no result was published in a peer-reviewed journal. The company's only registered trial, NCT00746824, tested a different molecule, its Y4-selective agonist TM30339, and was terminated in 2009. Development of obinepitide appears to have stopped.

Status as of this entry's last review, November 5, 2026. Approvals, compounding rules and sport rules change; the regulatory tracker is checked more often.

What the studies show

PubMed holds one record that names obinepitide, a 2024 review of the Y4 receptor and pancreatic polypeptide, carded below; it describes the drug's target and stage, not trial results. Everything known about obinepitide in people comes from 7TM Pharma's own announcements in the 2000s, none of them a peer-reviewed paper and none carried on ClinicalTrials.gov. The company said that in a phase I/II study in adults with obesity a once-daily injection under the skin lowered food intake for at least nine hours after dosing and was safe and well tolerated, that the study met its goals, and that it began a phase II study in obesity in 2007. It also reported that in obese animals the drug reduced weight over the long term more than PYY3-36. No numbers for weight change in people, and no trial report, were ever published, and development appears to have stopped.

Review · 2024

Review of the Y4 receptor and pancreatic polypeptide: where obinepitide fits

A review of the neuropeptide Y4 receptor and its natural partner pancreatic polypeptide, the satiety hormone released from the pancreas after a meal. It explains why the Y4 receptor is a target in obesity and surveys the ligands built on this system, naming obinepitide as a dual Y2/Y4 receptor agonist that reached clinical trials. The review reports no trial data of its own for the drug; it is carded here because it is the one PubMed record that names obinepitide and places it in its receptor class and development stage.

PMID 38430725

References

  1. [pubmed] Schüß C, et al. "Illuminating the neuropeptide Y(4) receptor and its ligand pancreatic polypeptide from a structural, functional, and therapeutic perspective." Neuropeptides, 2024;105:102416. PMID: 38430725.
  2. [other] ChEMBL molecule CHEMBL2108338 (OBINEPITIDE), read November 5, 2026: molecule type Protein; synonyms Obinepitide, Obinepitida, TM-30338 and TM30338; highest clinical phase recorded 2. https://www.ebi.ac.uk/chembl/compound_report_card/CHEMBL2108338/
  3. [other] FDA Global Substance Registration System / NCATS Inxight Drugs, Obinepitide, UNII 926PP306RV (CAS 348119-84-6; code names TM-30338 and TM30338), read November 5, 2026: a synthetic analogue of the pancreatic-polypeptide family, catalogued under the systematic name "(34-L-glutamine)pancreatic hormone (human)". https://drugs.ncats.io/drug/926PP306RV
  4. [other] DrugBank DB05045 (Obinepitide), read November 5, 2026: a synthetic analogue of the two meal-released human hormones PYY and pancreatic polypeptide, listed as a first-in-class compound that in one drug targets both the Y2 and the Y4 receptor; molecular formula C185H288N54O55S2, average mass 4212.78 Da; targets neuropeptide Y receptor type 2 (NPY2R, P49146) and type 4 (NPY4R, P50391); investigated in obesity. https://go.drugbank.com/drugs/DB05045
  5. [manufacturer] 7TM Pharma A/S announcement, reported March 22, 2006 (bionity.com, "7TM Pharma's new first-in-class anti-obesity drug completes Phase I/II clinical studies"): the company said TM30338 (obinepitide), a dual Y2-Y4 receptor agonist and synthetic analogue of PYY and pancreatic polypeptide, met both the primary and secondary objectives of a phase I/II study in obese adults, where once-daily subcutaneous dosing inhibited food intake at a statistically significant level up to at least 9 hours after dosing and the drug was safe and well tolerated; a larger phase IIa study was being planned. Company statements. https://www.bionity.com/en/news/53309. Read November 5, 2026.
  6. [manufacturer] 7TM Pharma A/S press release, reported June 12, 2007 (BioSpace, "7TM Pharma Initiates Phase II Clinical Study with the Drug Candidate Obinepitide for the Treatment of Obesity"): the company said it had started a phase II study of obinepitide (TM30338), described as a close analogue of two natural hormones with different mechanisms of action, for obesity and related diseases. Company statements. https://www.biospace.com/7tm-pharma-initiates-phase-ii-clinical-study-with-the-drug-candidate-obinepitide-for-the-treatment-of-obesity. Read November 5, 2026.
  7. [other] US FDA, Drugs@FDA and the drug label endpoint (openFDA), searched November 5, 2026: no application and no label record for obinepitide or TM30338.

Related peptides

Peptide YY

The postprandial 'stop eating' signal — an endogenous satiety peptide that reduces appetite via the Y2 receptor, and a pharmacological target for next-generation obesity drugs.

Pancreatic polypeptide

An islet hormone of the NPY family that curbs appetite; infused into volunteers it cut food intake by about a quarter, but its few-minute half-life has kept it a research tool.

Neuropeptide Y

The brain's most abundant neuropeptide — a 36-amino-acid master regulator of appetite, stress resilience, and anxiety that connects metabolic and cognitive peptide networks.

Semaglutide

A once-weekly GLP-1 receptor agonist FDA-approved for type 2 diabetes and chronic weight management.

Tirzepatide

A once-weekly GLP-1/GIP dual agonist that produced unprecedented weight loss in SURMOUNT trials — up to ~21% at highest dose.

Guides & tools

Disclaimer

This entry is for educational purposes only and does not constitute medical advice. Dosing information reflects published regulatory or research data and is not a recommendation. Many compounds described here are not approved for human use in the United States. Consult a licensed medical professional before considering any peptide therapy.