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Not Applicable
Epitomee Capsule for Weight Loss
N/A
Waitlist Available
Research Sponsored by Epitomee medical
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Females must be either surgically sterile or postmenopausal or agree to continue using an accepted method of birth control during the study
Be older than 18 years old
Must not have
Subjects who are habitual laxative users or using prescription medication for chronic constipation
Intending to undergo gastric surgery or gastric banding during the study period
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing the safety and effectiveness of the Epitomee Capsule in people who are overweight or obese, including those with prediabetes. The capsule helps people feel full and eat less, aiding in weight loss. Participants have already lost some weight using the capsule and will continue to use it along with lifestyle changes.
Who is the study for?
This trial is for adults with obesity or overweight and prediabetes who have lost at least 3% body weight in a previous study. They must be non-pregnant, able to use birth control if applicable, avoid NSAIDs (except low-dose aspirin or Celebrex), have stable psychiatric medication if used, and commit to a lifestyle program. A primary care physician and access to cellphone/internet are required.
What is being tested?
The Epitomee Capsule's extended use on body weight management is being tested in individuals with obesity/overweight conditions, some of whom may also have prediabetes. The study examines whether longer-term use can help maintain or further reduce body weight.
What are the potential side effects?
While the specific side effects of the Epitomee Capsule aren't listed here, similar treatments might cause digestive discomforts such as nausea or abdominal pain. Participants should report any new health changes that could relate to capsule usage.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am either surgically sterile, postmenopausal, or will use birth control during the study.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I regularly use laxatives or prescription medication for chronic constipation.
Select...
I plan to have stomach surgery or get a gastric band during the study.
Select...
I have stomach issues like ulcers, chronic pain, or nausea.
Select...
I have a condition that affects my esophagus, making it hard for things to pass through.
Select...
I have trouble swallowing or severe heartburn that medication doesn't help.
Select...
I experience recurring stomach pain, nausea, or vomiting after meals.
Select...
I have a blockage or serious condition in my digestive system.
Select...
I am currently on long-term steroids or medications that suppress my immune system.
Select...
I have started taking anti-platelet drugs other than low-dose Aspirin in the last 6 months.
Select...
I started taking medication for seizures or heart rhythm problems in the last 6 months.
Select...
My blood pressure is very high (160/100 mmHg or more).
Select...
I have heart issues like heart failure or had a heart attack or surgery within the last year.
Select...
I have a condition like irritable bowel syndrome or Crohn's disease.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in percent weight loss
Incidence, causality, and severity of serious adverse events, potentially related to Epitomee capsule
Secondary study objectives
Change in glycemic status (Normoglycemia, Prediabetes and Diabetes)
Change in plasma fasting glucose
Changes in BMI reduction
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Epitomee CapsuleExperimental Treatment1 Intervention
Epitomee Capsule combined with lifestyle counseling
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Epitomee Capsule
2021
N/A
~320
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for obesity often target appetite suppression and altered gastrointestinal function. Appetite suppressants, such as GLP-1 receptor agonists, work by mimicking hormones that signal fullness to the brain, thereby reducing food intake.
Treatments like the Epitomee Capsule aim to alter gastrointestinal function by expanding in the stomach to create a sense of fullness, which helps reduce calorie intake. These mechanisms are crucial for obesity patients as they directly address overeating and help manage weight by promoting a feeling of satiety, making it easier to adhere to a reduced-calorie diet.
Pharmacotherapy of obesity: emerging drugs and targets.
Pharmacotherapy of obesity: emerging drugs and targets.
Find a Location
Who is running the clinical trial?
Epitomee medicalLead Sponsor
3 Previous Clinical Trials
367 Total Patients Enrolled
2 Trials studying Obesity
357 Patients Enrolled for Obesity
Yael Kenan, DrStudy DirectorVP Clinical Affairs
1 Previous Clinical Trials
279 Total Patients Enrolled
1 Trials studying Obesity
279 Patients Enrolled for Obesity
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I will inform the study team about any changes in my health or medications.My mental health is stable, and I've been on the same psychiatric medication dose for 3 months.I am not using NSAIDs and am willing to avoid them, except for low-dose aspirin or Celebrex.I regularly use laxatives or prescription medication for chronic constipation.I plan to have stomach surgery or get a gastric band during the study.I have prediabetes and have been taking up to 2000 mg of metformin daily for at least a month.I have stomach issues like ulcers, chronic pain, or nausea.I have a condition that affects my esophagus, making it hard for things to pass through.I have trouble swallowing or severe heartburn that medication doesn't help.I experience recurring stomach pain, nausea, or vomiting after meals.I haven't taken any stomach-irritating medications for 4 weeks.I finished 24 weeks of the study and missed no more than two visits.I have a blockage or serious condition in my digestive system.I am not using NSAIDs and can avoid them, except for low-dose aspirin or Celebrex.I am currently on long-term steroids or medications that suppress my immune system.I am either surgically sterile, postmenopausal, or will use birth control during the study.I have started taking anti-platelet drugs other than low-dose Aspirin in the last 6 months.I started taking medication for seizures or heart rhythm problems in the last 6 months.My blood pressure is very high (160/100 mmHg or more).I have heart issues like heart failure or had a heart attack or surgery within the last year.I have a condition like irritable bowel syndrome or Crohn's disease.I started medication for high blood pressure or cholesterol less than a month ago.I don't have any health issues that could affect my participation in the study.I am willing to avoid substances that can change my weight during the study.You must have a primary care physician (PCP) who is responsible for providing routine care.I am a woman who is either surgically sterile, postmenopausal, or will use birth control during the study.
Research Study Groups:
This trial has the following groups:- Group 1: Epitomee Capsule
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Obesity Patient Testimony for trial: Trial Name: NCT04994769 — N/A
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