Amycretin
Novo Nordisk's single-molecule GLP-1 + amylin co-agonist. Phase 1/2 in oral and subcutaneous formulations. The pharmacological consolidation of the Semaglutide + Cagrilintide concept into one peptide.
Amycretin: Novo Nordisk's single-molecule GLP-1 + amylin co-agonist. Phase 1/2 in oral and subcutaneous formulations. The pharmacological consolidation of the Semaglutide + Cagrilintide concept into one peptide. Amycretin is Novo Nordisk's experiment in putting Semaglutide and Cagrilintide together as one molecule instead of two separate drugs.
Amycretin is Novo Nordisk's experiment in putting Semaglutide and Cagrilintide together as one molecule instead of two separate drugs. Activates GLP-1 + amylin in a single injection. They're testing both an oral pill and a weekly injection. Phase 1/2 only, not available yet.
Investigational. Phase 1/2 trials by Novo Nordisk in oral and subcutaneous formulations.
Trial access only.
Who it's for
- โTrial participants in obesity studies
- โFollowers of Novo's next-generation pipeline
- โEducational reference for dual co-agonist design
What to expect
- Week 1
Appetite drops. Some early-trial users reported faster onset than Semaglutide alone.
- Week 4
First titration step.
- Week 8
Phase 1b data showed weight loss outperforming Semaglutide-monotherapy comparators.
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How it works (mechanism)
Single-molecule co-agonist, activates GLP-1 AND amylin receptors simultaneously. Pharmacological consolidation of the CagriSema concept into one peptide instead of two.
Dosing protocol
Stacks well with
Side effects
When NOT to use
- โ MTC / MEN-2 history
- โ Pancreatitis history
- โ Pregnancy / nursing
Bloodwork to monitor
- โข Lipid panel
- โข A1C
- โข ALT/AST
Common mistakes
- โข Expecting trial-grade material from community vendors
- โข Treating it as available-now (Phase 1/2 still)
- โข Comparing oral form dosing to sub-q form dosing
What it actually is
Amycretin is Novo Nordisk's attempt to put GLP-1 and amylin agonism into a single molecule, rather than combining two drugs the way CagriSema does. It exists in both a weekly injectable and a daily oral form and is in early clinical development โ phase 1 and 2. It is not approved anywhere, and the reported weight loss in early trials was large enough to attract a great deal of attention on a very small evidence base.
GLP-1 and amylin produce satiety through different routes โ GLP-1 through the classic incretin pathway, amylin through the brainstem โ and hitting both produces more appetite suppression than either alone. CagriSema demonstrates that with two molecules. Amycretin does it with one, which simplifies manufacturing, dosing and the regulatory path considerably. The oral programme matters for the same reason it matters for any of these drugs: injection is the biggest adherence barrier in the class.
Forms, and which is which
Phase 1b/2a reported roughly 24% weight loss at 36 weeks at the highest doses tested. Identity, dose and monitoring known only here.
Verdict: The only defensible access.
A separate first-in-class oral programme with its own exposure profile. Not interchangeable with the injection at the same dose.
Verdict: A different drug exposure, not a convenience swap.
No approved product exists to compare against; identity and potency cannot be verified.
Verdict: Unverifiable contents outside any lawful route.
Semaglutide plus cagrilintide, the same pathway combination with phase 3 data behind it.
Verdict: The same idea, further along, in two molecules.
What it is claimed to do, graded
A phase 1b/2a trial published in the Lancet in 2025 reported roughly 24% weight loss at 36 weeks at the highest dose. A striking number from an early-phase trial in a small population.
The pharmacological premise, supported by the early data. No head-to-head against CagriSema exists.
A first-in-class oral programme has reported. Early, and the tolerability picture is not settled.
Suggested in early data and repeated widely. No head-to-head trial establishes it.
Phase 1 and 2 only. Nothing establishes durability or long-term safety, and 36 weeks in a small trial is not a safety profile.
Grades describe how much human evidence exists for that specific claim, not whether it will work for you or whether it is safe.
Pros and cons
- โข A genuinely elegant consolidation โ one molecule for a combination that currently needs two
- โข Early weight-loss figures are among the largest reported for any obesity drug at this stage
- โข Both injectable and oral programmes are running
- โข Published in the Lancet rather than announced only by press release
- โข Phase 1 and 2 only โ two indexed randomised-trial records in total
- โข The headline weight-loss figure comes from a small early-phase trial and will not necessarily survive phase 3
- โข Not approved anywhere; access is trial-only
- โข Gastrointestinal effects are common in the class and dose-dependent
- โข Nothing sold outside a trial can be verified
When to stop
- โข Severe persistent abdominal pain radiating to the back
- โข Vomiting that prevents keeping fluids down
- โข A new neck lump, hoarseness or difficulty swallowing
- โข Appetite suppression severe enough that protein intake has collapsed
- โข Pregnancy
Interactions
Additive glucose lowering expected from the GLP-1 arm. No approved interaction labelling exists.
Amycretin already does both jobs. Adding either duplicates half of it.
Delayed gastric emptying can alter absorption rate.
Compounds nausea and hypoglycaemia risk where intake is already low.
General weight-loss guidance, not an amycretin trial finding.
Is this for you?
- โข Participation in an authorised clinical trial is the only context in which this is lawfully available
- โข Anyone following where single-molecule incretin combinations are heading
- โข You want an approved medicine with a known safety profile
- โข Personal or family history of medullary thyroid carcinoma or MEN-2
- โข You are pregnant or nursing
- โข You are treating an early-phase headline number as a settled result
The one number
Sources for the claims above
- Amycretin, a unimolecular GLP-1 and amylin receptor agonist, phase 1b/2a
- First-in-class safety, tolerability, pharmacokinetics and pharmacodynamics
- Effect of amycretin on weight and metabolic markers
Drug & supplement interactions
- โ Combined GLP-1 + amylin warnings: insulin dose reduction; slowed oral absorption
- โ Trial-only, full interaction profile not yet published
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Common questions about Amycretin
Head-to-head with Amycretin
Tracked alongside Amycretin
Same goal, different aisle โ each graded on its own evidence in the Pepdex catalog.
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