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A Phase 3, Randomized, Double-Blind Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Participants with Obesity or Overweight

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2026-525408-82-00
Enrollment
184
Registered
2026-09-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Weight Management

Brief summary

Percent change from baseline of the parent trial in body weight, Incidence of treatment-emergent adverse events and serious adverse events

Detailed description

- Achieving ≥ 5% reduction from baseline of the parent trial in body weight - Achieving ≥ 10% reduction from baseline of the parent trial in body weight - Achieving ≥ 15% reduction from baseline of the parent trial in body weight - Achieving ≥ 20% reduction from baseline of the parent trial in body weight, Change from baseline of the parent trial in waist circumference, Change from baseline of the parent trial in the Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Physical Function Composite Score, Percent change from baseline in body weight, - No gain of body weight from baseline of > 3% - No gain of body weight from baseline of > 5%, - Percent maintenance of body weight reduction achieved in the parent trial - Maintaining ≥ 80% of the body weight reduction achieved in the parent trial

Interventions

Sponsors

Amgen Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percent change from baseline of the parent trial in body weight, Incidence of treatment-emergent adverse events and serious adverse events—

Secondary

MeasureTime frame
- Achieving ≥ 5% reduction from baseline of the parent trial in body weight - Achieving ≥ 10% reduction from baseline of the parent trial in body weight - Achieving ≥ 15% reduction from baseline of the parent trial in body weight - Achieving ≥ 20% reduction from baseline of the parent trial in body weight, Change from baseline of the parent trial in waist circumference, Change from baseline of the parent trial in the Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Physical Function Composite Score, Percent change from baseline in body weight, - No gain of body weight from baseline of > 3% - No gain of body weight from baseline of > 5%, - Percent maintenance of body weight reduction achieved in the parent trial - Maintaining ≥ 80% of the body weight reduction achieved in the parent trial—

Outcome results

None listed

Source: EU CTIS · Data processed: Sep 23, 2026