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NCT06858878: MARITIME-2

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

Active, enrolled Phase 3 Last updated 31 December 2025
What this trial tests

Phase 3 trial testing Maridebart cafraglutide in Type 2 Diabetes Mellitus (T2DM), Obesity, Overweight in 1,105 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
17 March 2025
Primary endpoint
21 January 2027
16 April 2027

Quick facts

Lead sponsorAmgen
PhasePhase 3
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment1,105
Start date17 March 2025
Primary completion21 January 2027
Estimated completion16 April 2027
Sites187 locations across Italy, Japan, United Kingdom, Germany, Hungary, Poland, South Korea, Argentina

Drugs / interventions tested

Conditions studied

Sponsor

Amgen — full company profile →

Who can join

Adults 18 to 99, any sex, with Type 2 Diabetes Mellitus (T2DM), Obesity, Overweight. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this study is to demonstrate that maridebart cafraglutide is superior to placebo for percent change in body weight.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Maridebart cafraglutide

Trials testing the same drug.

Other Amgen trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06858878.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing