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A research study to see how well CagriSema helps people with type 2 diabetes and excess body weight lose weight

Phase 3
Active, not recruiting
Conditions
Obesity, unspecified, (2) ICD-10 Condition: E11||Type 2 diabetes mellitus,
Registration Number
CTRI/2023/04/051486
Lead Sponsor
Novo Nordisk AS
Brief Summary

This study will look at how well the new medicine CagriSema helps people living with excess body weight and type 2 diabetes losing weight. Participants will either get CagriSema or a dummy medicine. Which treatment they get is decided by chance.

The study will last for about 1½ years. Women cannot take part if pregnant, breast-feeding or plan to get pregnant during the study period.

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
All
Target Recruitment
1200
Inclusion Criteria
  • 1.Male or female 2.Age above or equal to 18 years at the time of signing informed consent 3.
  • BMI greather than or equal to 27.0 kg per m2 4.
  • Diagnosed with type 2 diabetes mellitus greater than or equal to 180 days before screening 5.Treatment with either lifestyle intervention, or treatment with 1-3 marketed oral antidiabetic drugs (OAD)s (metformin, α-glucosidase inhibitors (AGI), glinides, sodium-glucose co-transporter 2 inhibitor (SGLT2i), thiazolidinediones, or sulphonylureas (SU)s as a single agent or in combination) according to local label 6.
  • Treatment with oral antidiabetic drugs should be stable (same drug(s), dose and dosing frequency) for at least 90 days before screening 7.
  • HbA1c below or equal to 10% (86 mmol/mol) as measured by the central laboratory at screening.
Exclusion Criteria
  • 1.Clinically significant or severe hypoglycaemia within 6 months before screening or history of hypoglycaemia unawareness.
  • 2.Renal impairment with estimated glomerular filtration rate (eGFR) below 30 mL per min per 1.73 m2 (below 45 mL per min per 1.73 m2 in participants treated with SGLT2i), as measured by the central laboratory at screening.
  • 3.Uncontrolled and potentially unstable diabetic retinopathy or maculopathy.
  • Verified by a fundus examination performed within 90 days before screening or in the period between screening and randomisation.
  • Pharmacological pupil-dilation is a requirement unless using a digital fundus photography camera specified for non-dilated examination.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Relative change in body weight1.Time Frame: | From baseline (week 0) to end of treatment | (week 68) | 2.Time Frame: From baseline | (week 0) to end of treatment (week 68)
weight reduction1.Time Frame: | From baseline (week 0) to end of treatment | (week 68) | 2.Time Frame: From baseline | (week 0) to end of treatment (week 68)
2.Achievement of greater than or equal to 5percent1.Time Frame: | From baseline (week 0) to end of treatment | (week 68) | 2.Time Frame: From baseline | (week 0) to end of treatment (week 68)
Secondary Outcome Measures
NameTimeMethod
Relative change in body weightTime Frame: From baseline (week 0) to week 20,Measured in percentage.
Change in waist circumferenceTime Frame: From baseline (week 0) to end of treatment (week 68),Measured in cm
Change in Systolic Blood Pressure (SBP)Time Frame: From baseline (week 0) to end of treatment (week 68),Measured in mmHg
Change in Quality Of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Physical Function scoreTime Frame: From baseline (week 0) to end of treatment (week 68) ,Score points
Achievement of more than or equal to 20 percent weight reductionTime Frame: From baseline (week 0) to end of treatment (week 68) Count of participant
Change in Glycated Haemoglobin (HbA1c)Time Frame: From baseline (week 0) to end of treatment (week 68) percentage-points
Change in Short Form-36 Version 2.0 (SF-36v2) Physical Functioning scoreTime Frame: From baseline (week 0) to end of treatment (week 68),Score points

Trial Locations

Locations (16)

Apollo Multispecialty Hospitals Limited

🇮🇳

Kolkata, WEST BENGAL, India

 All India Institute of Medical Sciences

🇮🇳

Delhi, DELHI, India

 Excel Endocrine Centre

🇮🇳

Kolhapur, MAHARASHTRA, India

BYL Nair Hospital and T N Medical College Department of endo

🇮🇳

Mumbai, MAHARASHTRA, India

Dr Sunil Gupta

🇮🇳

Nagpur, MAHARASHTRA, India

Gleneagles Hospital

🇮🇳

Hyderabad, TELANGANA, India

Government Medical College

🇮🇳

Kozhikode, KERALA, India

HCG Hospitals

🇮🇳

Ahmadabad, GUJARAT, India

Indian Institute of Diabetes,

🇮🇳

Thiruvananthapuram, KERALA, India

Lady Hardinge Medical College and S.S.K. Hospital

🇮🇳

Delhi, DELHI, India

Scroll for more (6 remaining)
Apollo Multispecialty Hospitals Limited
🇮🇳Kolkata, WEST BENGAL, India
Dr Tirthankar Chaudhury
Principal investigator
9831322394
tirthankarc05@gmail.com

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