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A Research Study to See How Well CagriSema Compared to Tirzepatide Helps People With Obesity Lose Weight

Phase 3
Active, not recruiting
Conditions
Obesity
Interventions
Registration Number
NCT06131437
Lead Sponsor
Novo Nordisk A/S
Brief Summary

This study will look at how well CagriSema compared to Tirzepatide helps people lower their body weight. CagriSema is a new investigational medicine developed by Novo Nordisk that combines Cagrilintide and Semaglutide. CagriSema is not yet being prescribed by doctors. Participant will get injections once a week throughout the treatment period. Participant will inject the study medicine under the skin with a pen injector in the thigh, stomach, or upper arm. After a first low dose, the study medicine will be gradually increased until reaching the planned dose (2.4 mg CagriSema or 15 mg Tirzepatide). The study will last for about one and a half year for each participant.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
809
Inclusion Criteria
  • Male or female
  • Age 18 years or above at the time of signing the informed consent
  • Body mass index (BMI) of ≥ 30.0 kilogram per square meter (kg/m^2)
Exclusion Criteria
  • Glycated haemoglobin (HbA1c) ≥ 6.5 % (48 millimoles per mole [mmol/mol]) as measured by the central laboratory at screening
  • History of type 1 or type 2 diabetes mellitus

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CagriSema 2.4 mg/2.4 mgCagrilintideParticipants will receive 2.4 mg cagrilintide and 2.4 mg semaglutide subcutaneously once-weekly (dose escalation period of 16 weeks) for up to 84 weeks.
CagriSema 2.4 mg/2.4 mgSemaglutideParticipants will receive 2.4 mg cagrilintide and 2.4 mg semaglutide subcutaneously once-weekly (dose escalation period of 16 weeks) for up to 84 weeks.
Tirzepatide 15 mgTirzepatideParticipants will receive 15 mg tirzepatide subcutaneously once-weekly (dose escalation period of 20 weeks) for up to 84 weeks.
Primary Outcome Measures
NameTimeMethod
To confirm non-inferiority of CagriSema versus tirzepatide: Relative change in body weightFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage (%).

Secondary Outcome Measures
NameTimeMethod
To confirm superiority of CagriSema versus tirzepatide: Relative change in body weightFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage (%).

Achievement of greater than or equal to (≥) 25% weight reductionFrom baseline (week 0) to end of treatment (week 84)

Count of participants.

Achievement of ≥ 30% weight reductionFrom baseline (week 0) to end of treatment (week 84)

Count of participants.

Change in waist circumferenceFrom baseline (week 0) to end of treatment (week 84)

Measured in centimeter (cm).

Change in systolic blood pressure (SBP)From baseline (week 0) to end of treatment (week 84)

Measured in millimeter of mercury (mmHg).

Change in diastolic blood pressure (DBP)From baseline (week 0) to end of treatment (week 84)

Measured in mmHg.

Relative change in lipids: Total cholesterolFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage.

Relative change in lipids: High-density lipoprotein (HDL) cholesterolFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage.

Relative change in lipids: Non-HDL cholesterolFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage.

Relative change in lipids: Low-density lipoprotein (LDL) cholesterolFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage.

Relative change in lipids: Very low-density lipoprotein (VLDL) cholesterolFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage.

Relative change in lipids: TriglyceridesFrom baseline (week 0) to end of treatment (week 84)

Measured in percentage.

Number of Treatment-emergent Adverse Events (TEAEs)From baseline (week 0) to end of study (week 90)

Count of events.

Number of Treatment Emergent Serious adverse events (TESAEs)From baseline (week 0) to end of study (week 90)

Count of events.

Trial Locations

Locations (45)

Great Lakes Clinical Trials

🇺🇸

Chicago, Illinois, United States

Univ of Colorado at Denver

🇺🇸

Aurora, Colorado, United States

Northeast Research Institute

🇺🇸

Fleming Island, Florida, United States

Univ of Alabama Birmingham

🇺🇸

Birmingham, Alabama, United States

Chambliss Clinical Trials LLC

🇺🇸

Montgomery, Alabama, United States

FDRC

🇺🇸

Costa Mesa, California, United States

Diablo Clinical Research, Inc.

🇺🇸

Walnut Creek, California, United States

East West Med Res Inst

🇺🇸

Honolulu, Hawaii, United States

Jacksonville Ctr For Clin Res

🇺🇸

Jacksonville, Florida, United States

South Broward Research LLC

🇺🇸

Miramar, Florida, United States

Hope Clin Res & Wellness

🇺🇸

Conyers, Georgia, United States

Endeavor Health

🇺🇸

Skokie, Illinois, United States

Evanston Premier Hlthcr Res

🇺🇸

Skokie, Illinois, United States

Midwest Inst For Clin Res

🇺🇸

Indianapolis, Indiana, United States

Northern Pines Hlth Ctr, PC

🇺🇸

Buckley, Michigan, United States

StudyMetrix Research LLC

🇺🇸

Saint Peters, Missouri, United States

Comprehensive Weight Ctrl Prog

🇺🇸

New York, New York, United States

University of North Carolina

🇺🇸

Chapel Hill, North Carolina, United States

Medication Mgmnt, LLC_Grnsboro

🇺🇸

Greensboro, North Carolina, United States

PharmQuest Life Sciences LLC

🇺🇸

Greensboro, North Carolina, United States

Accellacare_NC

🇺🇸

Raleigh, North Carolina, United States

Accellacare

🇺🇸

Wilmington, North Carolina, United States

New Venture Medical Research

🇺🇸

Wadsworth, Ohio, United States

Lynn Institute of Norman

🇺🇸

Norman, Oklahoma, United States

The University of Penn Center

🇺🇸

Philadelphia, Pennsylvania, United States

Clinical Res Collaborative

🇺🇸

Cumberland, Rhode Island, United States

Medical University Of South Carolina

🇺🇸

Charleston, South Carolina, United States

Coastal Carolina Res Ctr

🇺🇸

North Charleston, South Carolina, United States

Hillcrest Clinical Research

🇺🇸

Simpsonville, South Carolina, United States

Spartanburg Medical Research

🇺🇸

Spartanburg, South Carolina, United States

Holston Medical Group_Bristol

🇺🇸

Bristol, Tennessee, United States

Holston Medical Group

🇺🇸

Kingsport, Tennessee, United States

Amarillo Med Spec LLP

🇺🇸

Amarillo, Texas, United States

Elligo Clin Res Centre

🇺🇸

Austin, Texas, United States

UT Health University of Texas

🇺🇸

Bellaire, Texas, United States

Baylr Sctt White Rs Inst, Endo

🇺🇸

Dallas, Texas, United States

Velocity Clin Res, Dallas

🇺🇸

Dallas, Texas, United States

UT Southwestern Medical Center-CRU

🇺🇸

Dallas, Texas, United States

DCOL Ctr for Clin Res

🇺🇸

Longview, Texas, United States

Washington Cntr Weight Mgmt

🇺🇸

Arlington, Virginia, United States

Health Res of Hampton Roads

🇺🇸

Newport News, Virginia, United States

National Clin Res Inc.

🇺🇸

Richmond, Virginia, United States

Selma Medical Associates

🇺🇸

Winchester, Virginia, United States

Capital Clin Res Ctr,LLC

🇺🇸

Olympia, Washington, United States

Rainier Clin Res Ctr Inc

🇺🇸

Renton, Washington, United States

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