Obesity evidence dossier

MariTide (maridebart cafraglutide)

The main question is not only potency, but whether less-frequent dosing can improve long-term persistence. Phase 3 72-week efficacy and maintenance data are the next key read.

AmgenPhase 3Monthly or less-frequent injection under study
Weight loss score /10067
Comparison statusOther trial data · Includes treatment stops
EvidencePhase 2 · Sponsor disclosure
Follow-up52 weeks

Total weight loss

16.2%

MariTide Phase 2, Cohort A · highest reported arm · week 52 · Includes treatment stops

Placebo-adjusted

13.7%

Difference from placebo in the same study when reported.

Study context

GLP-1 receptor agonist / GIP receptor antagonist conjugate/Adults with obesity or overweight, without diabetes/465 participants across the study/52-week endpoint

Baseline: See the source for enrollment criteria

Ranked result & calculation

MariTide Phase 2, Cohort A · highest reported arm · 52 weeks

Adults with obesity or overweight, without diabetes. 465 participants across the study (not this dose arm alone).

Includes treatment stops. Treatment-policy results estimate outcomes regardless of stopping treatment.

Average weight loss
16.2%
Placebo group
2.5% loss
Beyond placebo
13.7 percentage points (arm subtraction)
Stopped due to adverse events
Not verified for this result

Score: 70% × 66.8 total-loss points + 30% × 66.3 beyond-placebo points = 67/100, rounded. Conversion scales

Alternative analysis assuming continued treatment: 19.9% total loss. This is not the result used for the headline score. Alternative analysis source ↗

Amgen, Phase 2 results ↗Phase 2 · Sponsor disclosure · Reviewed 2026-09-21

Evidence

Benchmark read

MariTide Phase 2, Cohort A: Includes treatment stops.

Diabetes data

Separate Phase 2 diabetes cohorts showed less weight loss than the non-diabetic obesity cohort.

Safety

Side effects and cautions

Discontinuation read

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

Common side effects

Gastrointestinal adverse events, especially nausea and vomiting during escalation, are the main tolerability watch item.

Main cautions

Not approved; Phase 3 needs to clarify dose spacing, discontinuations, maintenance, and safety with longer exposure.

Upcoming catalyst

What to watch next

No verified readout dateExpected

Does less-frequent dosing preserve substantial weight loss with manageable discontinuation?

Watch for: MARITIME Phase 3 results and treatment discontinuations. Trial completion dates should not be presented as promised data-release dates.

Source: Amgen, Q2 2026 results

Linked clinical trials

Trials in the saddl3 obesity snapshot

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

NCT06987695

Phase 3

Efficacy and Safety of Maridebart Cafraglutide in Adult Participants in Japan Who Have Obesity Disease

Amgen

Non-diabetic obesity

Active

Dec 17, 2025

NCT07037459

Phase 3

Maridebart Cafraglutide in Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity

Amgen

Non-diabetic obesity

Recruiting

Apr 2, 2026

NCT07037433

Phase 3

Evaluating the Impact of Maridebart Cafraglutide on Cardiovascular Outcomes in Participants With Atherosclerotic Cardiovascular Disease and Overweight or Obesity

Amgen

Non-diabetic obesity

Recruiting

Mar 27, 2026

NCT07441252

Phase 2

A Trial to Evaluate Efficacy and Safety of Maridebart Cafraglutide in Adults Living With Elevated Liver Fat and Obesity or Overweight

Amgen

Non-diabetic obesity

Recruiting

Apr 2, 2026

NCT06352892

Phase 1

A Study to Evaluate AMG 133 in Chinese Participants With Obesity or Overweight

Amgen

Non-diabetic obesity

Completed

Jan 8, 2026

NCT07310563

Phase 1

A Trial to Evaluate Interactions Between Antiemetic Medication and AMG 133 in Participants Living With Overweight or Obesity

Amgen

Non-diabetic obesity

Completed

Dec 30, 2025

NCT04478708

Phase 1

Single and Multiple Ascending Dose Study of AMG 133 in Participants With Obesity

Amgen

Non-diabetic obesity

Completed

Dec 10, 2025

NCT06976372

Phase 1

A Study to Evaluate AMG 133 Administered Subcutaneously in Participants With Overweight or Obesity

Amgen

Non-diabetic obesity

Completed

Oct 8, 2025

NCT06858878

Phase 3

Efficacy and Safety of Maridebart Cafraglutide in Adult Participants With Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight

Amgen

Type 2 diabetes / obesity

Active

Dec 31, 2025

NCT06858839

Phase 3

Evaluation of Maridebart Cafraglutide in Adult Participants Without Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight

Amgen

Type 2 diabetes / obesity

Active

Oct 20, 2025

NCT05669599

Phase 2

Dose-ranging Study to Evaluate the Efficacy, Safety, and Tolerability of AMG 133 in Adult Subjects With Overweight or Obesity, With or Without Type 2 Diabetes Mellitus

Amgen

Type 2 diabetes / obesity

Completed

Jan 20, 2026

Back to obesity comparisonAmgen, Phase 2 resultsBack to total weight loss