Study of Subcutaneously Administered ENT-03 for the Treatment of Obesity and Diabetes

NCT ID: NCT05925920

Last Updated: 2024-11-05

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 49 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-06-13
• Study Completion Date: 2024-12-06

Brief Summary

Single center, single-dose, randomized, placebo-controlled, dose-escalating study to evaluate, safety, tolerability, pharmacokinetics, and pharmacodynamics of escalating doses of ENT-03S in obese but otherwise healthy subjects and in subjects with obesity and Type 2 diabetes.

Conditions

Obesity; Diabetes Mellitus, Type 2

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: OTHER
• Blinding Strategy: TRIPLE

Study Groups

Active

Receive a single dose of ENT-03 sub-cutaneously

Group Type: ACTIVE_COMPARATOR

ENT-03

Intervention Type: DRUG

single dose of active drug

Placebo

Receive a single dose of placebo sub-cutaneously

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

single dose of placebo comparator

Interventions

ENT-03

single dose of active drug

Intervention Type: DRUG

Placebo

single dose of placebo comparator

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Subjects aged 18-70 years, both genders.

2. Healthy as determined by a physician, based on history, medical examination, vital signs, and laboratory tests.

3. Males that agree to use condoms for the duration of participation in the study.

4. Females of non-child-bearing potential (i.e., tubal ligation, hysterectomy, or postmenopausal).

5. Female patients of child-bearing potential with negative serum pregnancy tests and who agree to use double-barrier contraception during the study.

6. Subjects must be able to read, speak, and understand English and/or Spanish and provide written informed consent, and be willing and able to comply with study procedures.

7. Subjects must have a BMI 30-35 kg/m2 inclusive assessed immediately prior to screening.

8. Fasting insulin level ≥11 mIU/L.

9. HbA1c < 8.5% (diabetic subjects only).

10. Subjects with Type 2 diabetes on no anti-diabetic medication or on stable doses of metformin for 4 weeks or more (diabetic cohorts only).

11. No history of active or chronic disease other than that allowed by study: hypertension, hyperlipidemia, hyperglycemia, GERD, heartburn, or Type 2 diabetes (cohorts 6 and 7 only).

Exclusion Criteria

1. History of excessive alcohol use (defined as >21 drinks per week for males and >14 drinks per week for females), recreational drug use within the past three months, or failure on urinary drug screen.

2. Pregnant or breastfeeding within six months of screening assessment.

3. Substantial changes in eating habits or exercise routine within the preceding three months.

4. Evidence of eating disorders.

5. >5% weight change in the past three months.

6. Bariatric surgery within the past five years.

7. Significant renal impairment (eGFR <60 mg/mL/1.73m2).

8. Patients on anti-diabetic medications other than metformin.

9. Patients with gastroparesis.

10. Liver function tests (i.e., ALT, AST, alkaline phosphatase) greater than twice the upper limit of normal upon repeated measurements.

11. Diseases interfering with metabolism and/or ingestive behavior (e.g., myxedema, Cushing's disease, schizophrenia, major psychoses).

12. History of major depressive disorder within the previous two years, a lifetime history of suicide attempt, suicidal behavior within the previous month, or history of other severe psychiatric disorders.

13. Score of >15 on the Columbia Suicide Severity Rating Scale (C-SSRS).

14. Use of medications affecting body weight within the past three months:

• Drugs approved for the treatment of obesity
• Cyproheptadine or medroxyprogesterone
• Atypical anti-psychotic drugs
• Tricyclic antidepressants
• Lithium, MAO's, glucocorticoids
• SSRI's or SNRI's
• Antiepileptic drugs

15. Any clinically significant abnormality following the Investigator's review of the physical examination and clinical laboratory tests.

16. A baseline prolongation of QT/QTc interval after repeated measurements of >450 ms; a history of unexplained syncope, cardiac arrest, unexplained cardiac arrhythmias or torsades de pointes, structural heart disease, or a family history of Long QT Syndrome (LQTS).

17. Participation in an investigational drug trial within the month prior to dosing in the present study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Metabolics Pharma

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Richard Larson, MD

Role: STUDY_DIRECTOR

Enterin Inc.

Locations

ProSciento

San Diego, California, United States

Countries

United States

Other Identifiers

ENT-03S-22-001

Identifier Type: -

Identifier Source: org_study_id