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N/A N=436 Randomized Quadruple-blind Treatment

Study of Gelesis100 on Body Weight in Overweight and Obese Subjects With and Without Type 2 Diabetes

Overweight · Obesity

Enrolled (actual)
436
Serious AEs
0.2%
Results posted
Aug 2022
Primary outcome: Primary: Co-Primary Outcome: Percent Change in Body Weight — -6.41; -4.39 percentage change in body weight — p=0.0007

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Gelesis100 (Device); placebo (Device)
Age
Adult, Older Adult · 22+ yrs
Sex
All
Sponsor
Gelesis, Inc.
Primary completion
Jun 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Co-Primary Outcome: Percent Change in Body Weight
-6.41; -4.39 0.0007 sig
PRIMARY
Co-Primary Outcome: Percentage of Subjects Who Achieve Body Weight Loss ≥ 5%
58.6; 42.2 <0.0001 sig
SECONDARY
Percent Body Weight Change in Subjects With Impaired Plasma Glucose Status at Baseline
-6.46; -5.54
SECONDARY
Change in Plasma Glucose Status (Normal, Impaired, Diabetic) in Subjects With Impaired Plasma Glucose Status at Baseline.
23; 19; 35; 34; 1; 5
SECONDARY
Percent Change in Plasma Glucose
-2.39; -1.95
SECONDARY
Change in Body Mass Index (BMI)
-2.12; -1.51
SECONDARY
Change in Hemoglobin HbA1c in Subjects With Type 2 Diabetes at Baseline
-0.64; -3.06

Summary

This study will asses the decrease in body weight after repeated administration of Gelesis100 in overweight and obese subjects with and without Type 2 Diabetes.

Eligibility Criteria

Inclusion Criteria

  • Age 22 to 65 years of age, inclusive
  • Signed Informed Consent Form
  • BMI 27 to 40, inclusive (BMI of <30 should have at least one comorbidity)
  • Fasting plasma glucose 90mg/dL to 145 mg/dL, inclusive; non-diabetic normoglycemic (fasting glucose 90 mg/dL to 100 mg/dL, inclusive); non-diabetic impaired fasting glucose 100mg/dL to 126 mg/dL; and diabetic: untreated (126 mg/dL to 145 mg/dL, inclusive) and metformin-treated (metformin dose 1500mg/DL and less, fasting glucose less than 145 mg/dL, inclusive)

Exclusion Criteria

  • Pregnancy or lactation
  • Absence of medically approved contraceptive methods in females of childbearing potential
  • History of allergic reaction to modified cellulose, citric acid, sodium stearyl fumarate, raw cane sugar, gelatin, and titanium oxide
  • Administration of investigational products within 1 month prior to Screening Visit
  • Subjects who stopped smoking within 6 months prior to Screening Visit or considering smoking cessation during the study
  • Subjects anticipating surgical intervention during the study
  • Known Type 1 diabetes
  • History of eating disorders
  • Angina, coronary bypass, or myocardial infarction within 6 months prior to Screening Visit
  • History of: swallowing disorders, esophogeal anatomic abnormalities, gastroesophageal reflux disease, gastric or duodenal ulcer, gastroparesis (chronic nausea, vomiting, heartburn...), gastric bypass or other gastric surgery, intestinal obstruction or at high risk of including suspected small bowel adhesion, pancreatitis, malabsorption, history of bowel resection (except if related to appendectomy), history of abdominal radiation treatment
  • Laxative users
  • History of: HIV, hepatitis B or C; cancer within the past 5 years
  • Abnormal serum thyroid-stimulating hormone (TSH)
  • Positive urine drug test
  • Anti-obesity medication within 1 month prior to Screening Visit (except stable doses of metformin, no more than 1500 mg/day, for at leaset 1 month in subjects with type 2 diabetes)
  • Systemic corticosteroids within 1 month prior to Screening Visit
  • Thyroid hormones or preparations within 1 month prior to Screening Visit
  • Estrogen within 1 month prior to Screening Visit
  • Any other medication known to cause weight loss or weight gain within 1 month prior to Screening Visit
  • TSH suppression therapy for thyroid cancer
  • medications requiring mandatory administration with meal (lunch or dinner), except metformin
  • Other medication or product used for chronic diseases if their impaired gastrointestinal absorption can cause safety issues
  • Change in medications treating hypertension and/or dyslipidemia within 1 month prior to Screening Visit (including change in dose)
  • Anticipated requirement for use of prohibited concomitant medication
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02307279). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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