Obesity evidence dossier

Zenagamtide (amycretin)

Important to watch because amylin plus GLP-1 could become a major next-generation obesity approach if tolerability and durability hold up. Now in Phase 3, but no pivotal obesity efficacy figure is yet available to rank.

Novo NordiskPhase 3Oral and injectable formulations under study
Weight loss score /10094
Comparison statusOther trial data · Analysis not fully specified
EvidencePhase 1b/2a · Sponsor disclosure
Follow-up36 weeks

Total weight loss

24.3%

NN9490-7613 · 60 mg weekly, dose escalation · week 36 · Analysis not fully specified

Placebo-adjusted

23.2%

Difference from placebo in the same study when reported.

Study context

GLP-1/amylin co-agonist/Adults with obesity or overweight, without diabetes/125 participants across the study/36-week endpoint

Baseline: See the source for enrollment criteria

Ranked result & calculation

NN9490-7613 · 60 mg weekly, dose escalation · 36 weeks

Adults with obesity or overweight, without diabetes. 125 participants across the study (not this dose arm alone).

Analysis not fully specified. The source does not establish a treatment-policy analysis; interpret this score provisionally. Estimated change in the 60 mg dose-escalation arm; treatment-policy status is not established in this presentation.

Average weight loss
24.3%
Placebo group
1.1% loss
Beyond placebo
23.2 percentage points (arm subtraction)
Stopped due to adverse events
Not verified for this result

Early dose-escalation cohort; 125 is total study enrollment, not the size of this arm.

Score: 70% × 93.2 total-loss points + 30% × 95.1 beyond-placebo points = 94/100, rounded. Conversion scales

Novo Nordisk, Q2 2026 trial presentation ↗Phase 1b/2a · Sponsor disclosure · Reviewed 2026-09-21

Evidence

Benchmark read

NN9490-7613: Analysis not fully specified. Estimated change in the 60 mg dose-escalation arm; treatment-policy status is not established in this presentation. Early dose-escalation cohort; 125 is total study enrollment, not the size of this arm.

Diabetes data

Diabetes cohorts should be separated because glycemic status can materially change observed weight loss.

Safety

Side effects and cautions

Discontinuation read

Adverse-event discontinuation has not been verified for this result.

Common side effects

Gastrointestinal tolerability is the main expected watch item for GLP-1 and amylin-based escalation.

Main cautions

Not approved; the ~22% figure is an early 36-week adherence-based estimate at 20 mg subcutaneous, not a pivotal result. Dose selection and discontinuation rates in Phase 3 remain to be reported.

Upcoming catalyst

What to watch next

AMAZE Phase 3 readouts, dose strategy, and oral-versus-injectable positioning.

Linked clinical trials

Trials in the saddl3 obesity snapshot

Non-diabetic obesity studies are prioritized; diabetes and healthy-volunteer studies remain visible and labeled.

Back to obesity comparisonNovo Nordisk, Q2 2026 trial presentationBack to total weight loss