The Effect Of NS-0200 and NS-0300 Versus Placebo on Weight In Obesity

NCT ID: NCT03364335

Last Updated: 2019-08-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 267 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-01-08
• Study Completion Date: 2018-08-17

Brief Summary

This is a 24-week study to evaluate the effects of two fixed-dose combinations of leucine and sildenafil or two fixed-dose combinations of leucine, sildenafil and metformin compared to placebo. The primary objective of this study is to evaluate the percentage change in body weight in subjects from Baseline/Visit 2 (Day 1) to Study Termination/Visit 8 (Day 168/Week 24).

Detailed Description

This is a randomized, 24-week, placebo-controlled, double-blind study to evaluate the effects of two fixed-dose combinations of leucine and sildenafil or two fixed-dose combinations of leucine, sildenafil and metformin compared to placebo. Subjects meeting all the inclusion criteria and no exclusion criteria will be randomized to one of five study arms.

The primary objective of this study is to evaluate the percentage change in body weight in subjects from Baseline/Visit 2 (Day 1) to Study Termination/Visit 8 (Day 168/Week 24) receiving two fixed-dose combinations of leucine and sildenafil or two fixed-dose combinations of leucine, sildenafil and metformin compared to placebo. Secondary objectives will also assess changes in absolute body weight, percentage of patients with ≥5% body weight loss, change in waist circumference, change in HbA1c, change in fasting glucose, change in blood lipids such as cholesterol, LDL, HDL, triglycerides, change in blood pressure and changes in in C-reactive protein. In addition this study will evaluate the safety and tolerability of NS-0200 and NS-0300.

Patients will have one screening visits which will determine their eligibility based on lab tests. Once qualified, patients will be randomly assigned to either one of the treatment groups or the placebo control group and monitored for a total of 24 weeks. Patients will return to the clinic each month for lab tests, and routine examinations.

Conditions

Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Placebo

Each dose of placebo will consist of three tablets, identical in appearance to those used in the two active treatment arms, containing 93.5% Microcrystalline cellulose PH 102, 5.0% Crospovidone XL 10, 1.0% Silica gel (Syloid 244), 0.5% Magnesium stearate I MF3V for the leucine matched placebo and 99.5% Avicel PH200 , 0.5% magnesium stearate (w/w) and Opadry II White coating 3% weight gain for the sildenafil matched placebo.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo

Leu Sil 1.0mg

3 capsules BID consisting of 2 capsules containing 550 mg L-leucine each and 1 capsule containing 1.0 mg of sildenafil

Group Type: EXPERIMENTAL

Leu Sil 1.0mg

Intervention Type: DRUG

Leu 1100 mg + 1mg Sil BID

Leu Sil 4.0mg

Intervention Type: DRUG

Leu 1100 mg + 4mg Sil BID

Leu Sil 4.0mg

3 capsules BID consisting of 2 capsules containing 550 mg L-leucine each and 1 capsule containing 4.0 mg of sildenafil

Group Type: EXPERIMENTAL

Leu Sil 1.0mg

Intervention Type: DRUG

Leu 1100 mg + 1mg Sil BID

Leu Met Sil 1.0mg

Intervention Type: DRUG

Leu 1100 mg + Met 500mg + 1mg Sil BID

Leu Met Sil 1.0mg

3 capsules BID consisting of 2 capsules containing 550 mg L-leucine and 250 mg metformin and 1 capsule containing 1.0 mg of sildenafil

Group Type: EXPERIMENTAL

Leu Sil 1.0mg

Intervention Type: DRUG

Leu 1100 mg + 1mg Sil BID

Leu Sil 4.0mg

Intervention Type: DRUG

Leu 1100 mg + 4mg Sil BID

Leu Met Sil 4.0mg

Intervention Type: DRUG

Leu 1100 mg + Met 500mg + 4mg Sil BID

Leu Met Sil 4.0mg

3 capsules BID consisting of 2 capsules containing 550 mg L-leucine and 250 mg metformin and 1 capsule containing 4.0 mg of sildenafil

Group Type: EXPERIMENTAL

Leu Sil 1.0mg

Intervention Type: DRUG

Leu 1100 mg + 1mg Sil BID

Leu Met Sil 1.0mg

Intervention Type: DRUG

Leu 1100 mg + Met 500mg + 1mg Sil BID

Leu Met Sil 4.0mg

Intervention Type: DRUG

Leu 1100 mg + Met 500mg + 4mg Sil BID

Interventions

Leu Sil 1.0mg

Leu 1100 mg + 1mg Sil BID

Intervention Type: DRUG

Leu Sil 4.0mg

Leu 1100 mg + 4mg Sil BID

Intervention Type: DRUG

Leu Met Sil 1.0mg

Leu 1100 mg + Met 500mg + 1mg Sil BID

Intervention Type: DRUG

Leu Met Sil 4.0mg

Leu 1100 mg + Met 500mg + 4mg Sil BID

Intervention Type: DRUG

Placebo

Placebo

Intervention Type: DRUG

Other Intervention Names

NS-0300-1.0; NS-0300-4.0; NS-0200-1.0; NS-0200-4.0

Eligibility Criteria

Inclusion Criteria

1. Age ≥18 and ≤65 at study entry.

2. Is male, or female and, if female, meets all of the following criteria:

1. Not breastfeeding

2. Post-menopausal or negative serum pregnancy test result (human chorionic gonadotropin, beta subunit [β-hCG]) at Screening/Visit 1 (Day-7/Week-1) (not required for hysterectomized females)

3. If of childbearing potential (including peri-menopausal women who have had a menstrual period within one year) must practice and be willing to continue to practice appropriate birth control (defined as a method which results in a low failure rate, i.e., less than 1% per year, when used consistently and correctly, such as double barrier methods [male condom with spermicide, with or without cervical cap or diaphragm], implants, injectables, oral contraceptives [must have been using for at least the last 3 months], some intrauterine contraceptive devices, tubal ligation, or in an established relationship with a vasectomized or same sex partner) during the entire duration of the study

3. Stable body weight (±5%) and health over the last 3 months.

4. Has a BMI between 30 kg/m2 and 45 kg/m2

5. Stable diet within the last three months

Exclusion Criteria

7. Clinical laboratory tests (hematology, clinical chemistry, and urinalysis) either normal, not clinically significant or with abnormalities consistent with obesity

8. Is able to read, understand, and sign the informed consent forms (ICF) and, when applicable, an authorization to use and disclose protected health information form (consistent with Health Insurance Portability and Accountability Act of 1996 [HIPAA] legislation), communicate with the investigator, and understand and comply with protocol requirements.

1. Diagnosis of diabetes or on a diabetes medication

2. HbA1c ≥6.5% at Screening/Visit 1 (Day-7/Week-1)

3. Severe renal impairment (eGFR < 45 mg/mL/1.73 m2) and/or patients with acute or chronic metabolic acidosis. Acidosis is defined as >25mmol/L computed without K.

Normal is 8- 16, but acidosis is >25

4. Use of any of the following medications in the eight weeks prior to entering screening for study participation and during the study:

1. Use of any anti-diabetes medication including metformin and any combination drug that contains metformin

2. Sildenafil

3. Tadalafil

4. Vardenafil

5. OCT2/MATE inhibitors (e.g. cimetidine, quinidine, and pyrimethamine)

6. Riociguat (guanylate cyclase stimulant)

7. Alpha blockers

8. Nitrates (e.g. oral nitrates, sublingual nitroglycerine and nitroglycerine patches)

9. Potent CYP3A4 inhibitors (e.g. clarithromycin, telithromycin, nefazodone, itraconazole, ketoconazole, atazanavir, darunavir, indinavir, lopinavir, nelfinavir, ritonavir, saquinavir, tipranavir)

10. All antihypertensive medications

11. Medications associated with weight changes

• Drugs approved for the treatment of obesity
• Cypropheptadine or medroxyprogesterone
• Atypical anti-psychotic drugs
• Tricyclic antidepressants
• Lithium, MAO's, glucocorticoids
• SSRI's or SNRI's
• Antiepileptic drugs
• Systemic corticosteroids
• Stimulants e.g. amphetamines

12. Any dietary supplement that is labeled for weight management or maintenance of healthy weight

5. Diagnosis or evidence of eating disorders

6. ≥ 5% weight change in the last 3 months

7. Subjects who have had bariatric surgery

8. An infection requiring antibiotic treatment within the last 30 days

9. Any chronic inflammatory disease, e.g. inflammatory bowel disease rheumatoid arthritis, vasculitis, systemic lupus erythematosus

10. Diseases interfering with metabolism (including metabolism of branched chain amino acids) and/or ingestive behavior (myxedema, Cushing's disease, diabetes, schizophrenia, major psychoses, maple syrup urine disease, unmanaged depression etc.)

11. History of alcohol abuse (defined ≥ 21 drinks per week for males and > 14 drinks per week for females), within the past 3 months or failure on urinary drug screen

12. History of substance abuse (including alcohol abuse as defined above) in the past 12 months or a positive screen for drugs (opioids without a prescription), including marijuana, of abuse or alcohol at screening.

13. Has received any investigational drug within 3 months of Screening.

14. Has donated blood within 3 months before Screening or is planning to donate blood during the study (due to HbA1c reading at screening)

15. Other medical conditions that may diminish life expectancy to <2 years, including known cancers

16. Have been diagnosed with metastatic carcinomas in the last 5 years

17. Has known allergies or hypersensitivity to metformin, sildenafil or leucine

18. Have suffered myocardial infarction, stroke, arrhythmia in the last 6 months

19. Resting hypotension (BP <90/50 mmHg) or severe hypertension (BP >170/110 mmHg) If both or one of the parameters for diastolic or systolic BP is meet

20. Cardiac failure or coronary artery disease causing unstable angina

21. History or evidence at screening of left ventricular outflow obstruction (e.g., aortic stenosis, idiopathic hypertrophic subaortic stenosis) and those with severely impaired autonomic control of blood pressure

22. At risk for priapism due to anatomical deformation of the penis (e.g., angulation, cavernosal fibrosis, Peyronie's disease) or other conditions that predispose to priapism (e.g., sickle cell anemia, multiple myeloma, or leukemia)

23. Clinical evidence of hepatic impairment and/or ALT/AST >5X ULN

24. Is an immediate family member (spouse, parent, child, or sibling; biological or legally adopted) of personnel directly affiliated with the study at the clinical study site, or NuSirt Biopharma.

25. Is employed by NuSirt Biopharma (defined as an employee, temporary contract worker, or designee responsible for the conduct of the study).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

NuSirt Biopharma

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Michael B Zemel, PhD

Role: STUDY_CHAIR

NuSirt Biopharma

Locations

AMR

Mobile, Alabama, United States

Catalina Research Institute

Montclair, California, United States

Northern California Research

Sacramento, California, United States

ACR

Meridian, Idaho, United States

Synexus

Chicago, Illinois, United States

Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States

Clinical Trials Management

Metairie, Louisiana, United States

Synexus

St Louis, Missouri, United States

AMR

Las Vegas, Nevada, United States

Rapid Medical Research

Cleveland, Ohio, United States

Medical Research South

Charleston, South Carolina, United States

Premier

Clarksville, Tennessee, United States

Synexus

Dallas, Texas, United States

Synexus

San Antonio, Texas, United States

ACR

Jordan, Utah, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

NS-WM-01

Identifier Type: -

Identifier Source: org_study_id