Status:
NOT_YET_RECRUITING
One-Year Study of S1B-509 vs Placebo for Weight Loss
Lead Sponsor:
S1 Biopharma, Inc.
Conditions:
Obesity
Eligibility:
All Genders
25-70 years
Phase:
PHASE2
Brief Summary
This is a study to test whether S1B-509 given orally daily helps people with overweight or obesity to lose more weight than with placebo over a year.
Detailed Description
This trial is to determine proof of concept for S1B-509 vs. placebo and to define a suitable dose escalation scheme and range for S1B-509 regarding safety, tolerability, and efficacy. The treatments w...
Eligibility Criteria
Inclusion
- Patients with obesity disease and inadequately controlled body weight with diet and/or exercise
- Body mass index (BMI) ≥ 27 kg/m2 with significant comorbidity, e.g., type 2 diabetes, hypertension, dyslipidemia, sleep apnea, cardiovascular disease
- Waist circumference at umbilical level ≥ 85 cm for male, ≥ 90 cm for female
- Visceral fat area ≥ 100 cm2
- Agreement to comply with the study-required life-style intervention and treatment during the full duration of the study.
- Side effects from any continuing concomitant medications must be mild and stable or nil.
- Females: not pregnant or lactating for six months; using medically reliable contraception, i.e., diaphragm or (male or female) condom and spermicide, IUD, tubal sterilization, hormonal contraception (oral, vaginal, or implant), or (if the investigator finds the patient credibly monogamous) vasectomy of male partner.
- Gives informed consent for and is willing to undergo all of the scheduled evaluations.
- Prompt for screening and baseline visits, is cooperative, and takes reasonable directions without excessive explanations.
Exclusion
- Use of pharmacologically active weight-loss medications, glucagon-like peptide-1 (GLP-1) agonists or sodium-glucose co-transporter 2 (SGLT2) inhibitors, within 3 months of screening, or between screening and randomization.
- Use of alpha glucosidase inhibitors within 3 months of Visit 1, or between screening and randomization.
- Bariatric surgery
- Lack of compliance with lifestyle intervention (defined as weight gain during 4-week Screening/run-in or with study medication (defined as \< 80% study drug intake in more than one 4-week period
- History of ketoacidosis, lactic acidosis, or hyperosmolar coma, or any of these occurring between Visit 1 and 2/randomization
- Diabetics with HbA1c levels over 10 percent or fasting glucose levels greater than or equal to 270 mg/dl.
- Symptomatic infection in the 4 weeks prior to screening or randomization.
- Gastro-intestinal (GI) disorders associated with chronic diarrhea.
- Congestive heart failure, New York Heart Association (NYHA) class III or IV
- Body dysmorphic disorder or compulsive eating disorder
- Chronic conditions that may in the investigator's judgment be expected to be unstable and affect overall health are not allowed. Examples: gastrointestinal bleeding in prior 6 months, diabetes mellitus with HB A1C \>8.9, asthma not well controlled with treatment once or twice daily, current Major Depressive Disorder or recurrence of MDD off treatment for at least 2 months, anxiety disorder severe enough to prevent employment, severe sleep apnea, history within the prior year of suicidality or drug abuse, history of active breast, cervical, uterine, ovarian or other systemic cancer within the prior 24 months.
- Requires CYP3A4, CYP 2B6, or CYP 2D6 strong inhibitor or inducer drugs
- Takes any sex hormone other than an approved hormonal contraceptive
- Takes an antiepileptic/mood stabilizer, antipsychotic, antidepressant, anxiolytic, or hypnotic drug
- Drinks more than 7 alcoholic drinks per week (12-oz beer, 4-oz wine, 1 ½ oz liquor etc)
- Uses marijuana more than once a week
- History of seizures as an adult or use of antiepileptic medication
- Long QT syndrome (QTc \<=480 msec), other significant cardiovascular disease (hypertension controlled with one medication is acceptable)
- Moderate or severe dysfunction of the liver (any LFT \>=3x ULN) or renal dysfunction (BUN \> 30 or Cr \>2.0)
- Uses sedating antihistamines or prescription sedatives daily
- History of blood clots or abnormal bleeding tendencies, including daily use of medications adversely affecting coagulation, e.g., NSAIDs, systemic corticosteroids, or \>81 mg aspirin daily.
Key Trial Info
Start Date :
October 15 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 15 2027
Estimated Enrollment :
210 Patients enrolled
Trial Details
Trial ID
NCT06517797
Start Date
October 15 2025
End Date
December 15 2027
Last Update
June 18 2025
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.