Two additional retatrutide Phase 3 trials reported
Lilly announced topline results from TRIUMPH-2 and TRIUMPH-3. Retatrutide remains investigational and is not approved by a regulatory authority.
Primary source ↗A LOOK AT METABOLIC PEPTIDES
Retatrutide, cagrilintide, survodutide, zenagamtide and MariTide. See how they differ, what their programmes study and where the clinical science stands.
Educational guide. Treatment choices belong in a conversation with a clinician.

External research catalogues may include materials labelled for laboratory research only. They are not presented here as medicines, personal-use products or approved therapeutic products.
01 / WHAT’S NEW
New molecules, trial results, regulatory filings and approvals, ordered by publication date and linked to primary sources.
Lilly announced topline results from TRIUMPH-2 and TRIUMPH-3. Retatrutide remains investigational and is not approved by a regulatory authority.
Primary source ↗The company announced additional Phase 3 CagriSema results and mid-stage data for investigational zenagamtide ahead of ADA 2026.
Primary source ↗Novo Nordisk filed a US application for weight management. A filing is not an approval; CagriSema remains investigational while the review is pending.
Primary source ↗A trial result or regulatory filing is not an approval. We will label an approval only after publication by the relevant regulator.
02 / RESEARCH CATALOGUE
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03 / MOLECULES IN FOCUS
These profiles describe molecules in clinical development. Trial data do not establish the quality or safety of products sold by online stores.

GLP-1 + GIP + glucagon
A triple receptor agonist studied in obesity and related conditions. Lilly describes it as an investigational molecule that is not yet approved for use.

GLP-1 + glucagon
A dual receptor agonist studied in overweight and obesity. The clinical programme evaluates both efficacy and safety.

Amylin analogue
A different hormonal approach studied alone and with semaglutide. CagriSema is a separate investigational combination; its results are not results for cagrilintide alone.

GLP-1 + amylin
A unimolecular GLP-1 and amylin receptor agonist. Novo Nordisk describes zenagamtide (amycretin) as an investigational molecule in clinical development, including Phase 3 programmes; it is not an approved medicine.

GLP-1 + GIPR antagonism
An antibody-peptide conjugate studied in the MARITIME programme. Amgen describes MariTide as an investigational molecule in Phase 3; a clinical programme is not regulatory approval.
These profiles are not a ranking and are not a recommendation for use. Regulatory status can change.
04 / CLINICAL DATA IN NUMBERS
These are results from specific trials, doses and time periods. They are not a promise of an individual outcome and do not validate products sold through an online catalogue.
At 48 weeks at the highest studied dose, compared with −2.1% for placebo.
NEJM ↗At 46 weeks at 4.8 mg; the planned-treatment analysis was −14.9% versus −2.8% for placebo.
PubMed ↗REDEFINE 1 reported −20.4% in the treatment-policy analysis; −22.7% was the estimate if all participants adhered to treatment.
Novo Nordisk ↗Different molecules, doses, participants and analyses should not be turned into a simple ranking. Investigational programmes and research-only catalogue products are separate categories.
05 / HOW TO READ THE DATA
Trial results depend on the participants, duration and analysis method. A percentage alone is not enough for a comparison.
Example of regulatory assessment: EMA ↗
Check whether participants had diabetes, the inclusion criteria and how long they were followed.
A placebo comparison and a head-to-head medicine trial answer different questions.
Adverse events and treatment discontinuation are part of the assessment. Results do not guarantee an individual effect.
06 / APPROVED MEDICINES
In the EU, specific prescription medicines are approved for weight management. That approval does not transfer to other products with a similar name or composition.
Wegovy — a prescription medicine with weight-management indications for defined patient groups.
Indications and risks at EMA ↗Mounjaro — a prescription medicine with indications that include weight management in defined adult groups.
Indications and risks at EMA ↗These are regulatory examples, not an offer of sale or individual treatment advice. Discuss options with a clinician.
07 / OTHER AREAS
Peptide science includes approved medicines and investigational programmes across many fields. This is a map of research, not a product list.
Insulin, GLP-1 and combination molecules are studied for glucose control, appetite and metabolic risk.
Peptide hormone analogues, including PTH-based therapies, are part of medicine development for bone loss.
Peptide carriers and peptide-drug conjugates are studied to deliver active molecules more precisely.
Peptides and growth factors are investigated for chronic wounds and tissue repair, with different clinical statuses.
Overview of therapeutic areas: PubMed review ↗ EMA links point to approved medicines for defined indications.
09 / FAQ
There is no universal choice. Approved indications, contraindications, other conditions and monitoring matter. A clinician can assess treatment options. Results from different trials are not automatically comparable.
Retatrutide is an investigational molecule in clinical development and is not approved for use. A published trial result is not authorization to sell it as a medicine.
No. Materials labelled for research use are not presented here as medicines or as products for personal use. A certificate of analysis does not turn them into approved medicines.
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