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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.
To asses the decrease in body weight after repeated administration of Gelesis100 in overweight and obese subjects with and without Type 2 Diabetes.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Gelesis100 | Experimental | Gelesis100 twice daily |
|
| Placebo | Placebo Comparator | Matching placebo twice daily |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Gelesis100 | Device |
| ||
| placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Co-Primary Outcome: Percent Change in Body Weight | Percent change in body weight from Baseline to Day 171 is presented. | Baseline to Day 171 |
| Co-Primary Outcome: Percentage of Subjects Who Achieve Body Weight Loss ≥ 5% | Percentage of participants who achieve a body weight loss ≥ 5% from Baseline to Day 171 is presented. | Baseline to Day 171 |
| Measure | Description | Time Frame |
|---|---|---|
| Percent Body Weight Change in Subjects With Impaired Plasma Glucose Status at Baseline | Impaired plasma glucose status is defined as Fasting Plasma Glucose (FPG) ≥100mg/dL and <126mg/dL at baseline measurement. | Baseline to Day 171 |
| Change in Plasma Glucose Status (Normal, Impaired, Diabetic) in Subjects With Impaired Plasma Glucose Status at Baseline. |
| Measure | Description | Time Frame |
|---|---|---|
| Assess Safety and Tolerability of Administration of Gelesis100 | Adverse Events (AEs), Physical Examinations, Vital Signs, Laboratory Tests | Baseline to Day 197 |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Hassan M Heshmati, MD | Chief Medical Officer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Investigative Site | Anaheim | California | 92801 | United States | ||
| Investigative Site |
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| ID | Title | Description |
|---|---|---|
| FG000 | Gelesis100 | Gelesis100 twice daily Gelesis100 |
| FG001 | Placebo | Matching placebo twice daily placebo |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Aug 24, 2016 |
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Normal plasma glucose status is defined FPG ≤ 100mg/dL. Impaired plasma glucose status is defined as FPG ≥100mg/dL and <126mg/dL. Diabetic plasma glucose status was defined as FPG >126mg/dL. |
| Baseline to Day 171 |
| Percent Change in Plasma Glucose | Percent change in Plasma Glucose in subjects with impaired glucose and T2D at baseline. Impaired plasma glucose is defined as FPG≥100mg/dL and FPG<126mg/dL. | Baseline to Day 171 |
| Change in Body Mass Index (BMI) | The BMI was calculated using height (in cm) and weight (in kg) according to the following formula: BMI (kg/m2((superscript 1)) = Weight (kg)/[Height (cm)/100]2(superscript2). | Baseline to Day 171 |
| Change in Hemoglobin HbA1c in Subjects With Type 2 Diabetes at Baseline | To assess the decrease in HbA1c after repeated administration of Gelesis 100 over a period of 168 days in overweight and obese people with type 2 diabetes, The glycosylated hemoglobin was measured in mmol/mol. | Baseline to Day 171 |
| San Diego |
| California |
| 92103 |
| United States |
| Investigative Site | Tustin | California | 92780 | United States |
| Investigative Site | Walnut Creek | California | 94598 | United States |
| Investigative Site | West Hills | California | 91307 | United States |
| Investigative Site | Aurora | Colorado | 80045 | United States |
| Investigative Site | Jacksonville | Florida | 32205 | United States |
| Investigative Site | Miami | Florida | 33143 | United States |
| Investigative Site | Boise | Idaho | 83642 | United States |
| Investigative Site | Chicago | Illinois | 60208 | United States |
| Investigative Site | Baton Rouge | Louisiana | 70808 | United States |
| Investigative Site | Boston | Massachusetts | 02115 | United States |
| Investigative Site | Las Vegas | Nevada | 89401 | United States |
| Investigative Site | New York | New York | 10065 | United States |
| Investigative Site | Raleigh | North Carolina | 27612 | United States |
| Investigative Site | Cincinnati | Ohio | 45219 | United States |
| Investigative Site | Columbus | Ohio | 43212 | United States |
| Investigative Site | Columbus | Ohio | 43213 | United States |
| Investigative Site | Danville | Pennsylvania | 17822 | United States |
| Investigative Site | Nashville | Tennessee | 37203 | United States |
| Investigative Site | Dallas | Texas | 75246 | United States |
| Investigative Site | Round Rock | Texas | 78681 | United States |
| Investigative Site | West Jordan | Utah | 84088 | United States |
| Investigative Site | Norfolk | Virginia | 23606 | United States |
| Investigative Site | Richmond | Virginia | 23294 | United States |
| Investigative Site | Ottawa | Ontario | K1N 6N5 | Canada |
| Investigative Site | Québec | Quebec | G1V 0A6 | Canada |
| Investigative Site | Hradec | 500 00 | Czechia |
| Investigative Site | Prague | 121 08 | Czechia |
| Investigative Site | Prague | 140 00 | Czechia |
| Investigative Site | Prague | 182 00 | Czechia |
| Investigative Site | Copenhagen | DK-1958 | Denmark |
| Investigative Site | Milan | Milanese | 20097 | Italy |
| Investigative Site | Naples | 80131 | Italy |
| Investigative Site | Rome | 00161 | Italy |
| Investigative Site | Pamplona | 31008 | Spain |
| COMPLETED |
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| NOT COMPLETED |
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All 436 randomized subjects were included in the ITT population and 434 (99.5%) subjects were included in the Safety Population. Two randomized subjects never received IP and were excluded from the Safety Population.
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| ID | Title | Description |
|---|---|---|
| BG000 | Gelesis100 | Gelesis100 twice daily Gelesis100 |
| BG001 | Placebo | Matching placebo twice daily placebo |
| BG002 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | The age inclusion criteria used was ≥ 22 years and ≤ 65 years. | Count of Participants | Participants |
| |||||||||||||||||
| Sex: Female, Male | All male and female ambulatory subjects who met all inclusion criteria and no exclusion criteria were allowed to participate in the study. | Count of Participants | Participants |
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| Ethnicity (NIH/OMB) | Ambulatory subjects who met all inclusion criteria and no exclusion criteria were allowed to participate in the study regardless of ethnicity | Count of Participants | Participants |
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| Race/Ethnicity, Customized | Ambulatory subjects who met all inclusion criteria and no exclusion criteria were allowed to participate in the study regardless of race/ethnicity. | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
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| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Primary | Co-Primary Outcome: Percent Change in Body Weight | Percent change in body weight from Baseline to Day 171 is presented. | Overall number of patients analyzed is equal to the intention to treat population (all randomized subjects). | Posted | Mean | Standard Deviation | percentage change in body weight | Baseline to Day 171 |
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| Primary | Co-Primary Outcome: Percentage of Subjects Who Achieve Body Weight Loss ≥ 5% | Percentage of participants who achieve a body weight loss ≥ 5% from Baseline to Day 171 is presented. | Overall Number of Participants Analyzed is equal to the intention to treat population (all randomized subjects). | Posted | Number | percentage of participants | Baseline to Day 171 |
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| Secondary | Percent Body Weight Change in Subjects With Impaired Plasma Glucose Status at Baseline | Impaired plasma glucose status is defined as Fasting Plasma Glucose (FPG) ≥100mg/dL and <126mg/dL at baseline measurement. | Overall Number of Participants Analyzed is equal to the number of participants with impaired fasting glucose at Baseline. | Posted | Mean | Standard Deviation | percentage change in body weight | Baseline to Day 171 |
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| Secondary | Change in Plasma Glucose Status (Normal, Impaired, Diabetic) in Subjects With Impaired Plasma Glucose Status at Baseline. | Normal plasma glucose status is defined FPG ≤ 100mg/dL. Impaired plasma glucose status is defined as FPG ≥100mg/dL and <126mg/dL. Diabetic plasma glucose status was defined as FPG >126mg/dL. | Overall Number of Participants Analyzed is equal to the number of participants with impaired fasting glucose at Baseline. | Posted | Number | participants | Baseline to Day 171 |
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| Secondary | Percent Change in Plasma Glucose | Percent change in Plasma Glucose in subjects with impaired glucose and T2D at baseline. Impaired plasma glucose is defined as FPG≥100mg/dL and FPG<126mg/dL. | Overall Number of Participants Analyzed is equal to the number of participants with impaired fasting glucose at Baseline. | Posted | Mean | Standard Deviation | percentage of change in plasma glucose | Baseline to Day 171 |
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| Secondary | Change in Body Mass Index (BMI) | The BMI was calculated using height (in cm) and weight (in kg) according to the following formula: BMI (kg/m2((superscript 1)) = Weight (kg)/[Height (cm)/100]2(superscript2). | Overall number of patients analyzed is equal to the number of all participants with available data. | Posted | Mean | Standard Deviation | kg/m^2 | Baseline to Day 171 |
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| Secondary | Change in Hemoglobin HbA1c in Subjects With Type 2 Diabetes at Baseline | To assess the decrease in HbA1c after repeated administration of Gelesis 100 over a period of 168 days in overweight and obese people with type 2 diabetes, The glycosylated hemoglobin was measured in mmol/mol. | Overall number of patients analyzed is equal to the number of all participants with type 2 diabetes at baseline. | Posted | Mean | Standard Deviation | mmol/mol | Baseline to Day 171 |
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| Other Pre-specified | Assess Safety and Tolerability of Administration of Gelesis100 | Adverse Events (AEs), Physical Examinations, Vital Signs, Laboratory Tests | Not Posted | Baseline to Day 197 | Participants |
From screening (Day -21) to Day 197. The adverse device effect (AE) and the serious adverse device effects (SAE) are collected since screening until 28 days after the last administration of the investigational medical device.
AE reported by subjects are recorded and discussed in detail by the investigator at each visit.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Gelesis100 | Gelesis100 twice daily Gelesis100 | 0 | 223 | 0 | 223 | 159 | 223 |
| EG001 | Placebo | Matching placebo twice daily placebo | 0 | 211 | 1 | 211 | 149 | 211 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Colon Adenoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | Systematic Assessment |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Abdominal Distention | Gastrointestinal disorders | Systematic Assessment |
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| Abdominal pain | Gastrointestinal disorders | Systematic Assessment |
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| Constipation | Gastrointestinal disorders | Systematic Assessment |
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| Diarrhoea | Gastrointestinal disorders | Systematic Assessment |
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| Flatulence | Gastrointestinal disorders | Systematic Assessment |
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| Infrequent bowel movements | Gastrointestinal disorders | Systematic Assessment |
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| Nausea | Gastrointestinal disorders | Systematic Assessment |
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| Nasopharyngitis | Infections and infestations | Systematic Assessment |
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| Upper respiratory tract infections | Infections and infestations | Systematic Assessment |
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| Arthralgia | Musculoskeletal and connective tissue disorders | Systematic Assessment |
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| Headache | Nervous system disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Harry Leider, MD, MBA | Gelesis | (443)934-4906 | hleider@gelesis.com |
| Jan 21, 2022 |
| Prot_SAP_000.pdf |
| ID | Term |
|---|---|
| D050177 | Overweight |
| D009765 | Obesity |
| ID | Term |
|---|---|
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
| D001835 | Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| >=65 years |
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| Male |
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| Not Hispanic or Latino |
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| Unknown or Not Reported |
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| Black or African American |
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| Asian |
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| Other |
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| American Indian or Alaska Native |
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| Native Hawaiian or Other Pacific Islander |
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| United States |
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Super-Superiority (>3% difference), H0: μ(Placebo)-μ(Gelesis100) < 3% |
| ANCOVA |
Adjusted for stratification factors, and baseline weight |
| 0.1193 |
| Superiority |
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