Investigation of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LIM-0705 in Male Subjects With Impaired Glucose Tolerance

Phase 1

Withdrawn

• Conditions: Impaired Glucose Tolerance
• Interventions: Drug: LIM-0705; Drug: Placebo

• Registration Number: NCT01093677
• Lead Sponsor: Limerick BioPharma

Brief Summary

LIM-0705 will gain results on the effects of LIM-0705 on Male Subjects with Impaired Glucose Tolerance

Detailed Description

Not available

Study Timeline

• Study Start: 2010-03
• Study First Submitted: 2010-03-15
• Study First Submitted QC: 2010-03-25
• Study First Posted: 2010-03-26
• Status Verified: 2010-06
• Primary Completion: 2010-06
• Last Update Submitted: 2010-06-04
• Last Update Posted: 2010-06-08
• Study Completion: 2010-07

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: Male
• Target Recruitment: 30

Inclusion Criteria

1. Males, age 18-70 years old

2. Measured waist circumference to hip circumference ratio >0.90

3. Body mass index (BMI) of 27 - 40 kg/m2

4. Screening and Day -1 capillary glucose measurement between 110-160 mg/dL (6.1-8.9 mmol/L) after a 12 hour fast

5. Screening and Day -1 OGTT with a 2 hour post-glucose measurement ≥140 mg/dL (7.8 mmol/L) after a 12 hour fast

6. Screening HbA1c > 6 and ≤ 7.5%

7. Subjects must be in reasonably good health as determined by pre-study medical history, physical examination, 12-lead ECG, and the following laboratory measures:

   • Electrolytes, ALP, LDH, creatinine, and urea must be within normal range without medication
   • Urinalysis within normal limits

8. Willing to remain in confinement at the clinical study unit for up to 18 days/17 nights and to return to the unit as specified for additional assessments

9. Willing to consume only the food that is provided by the clinical study unit

10. Non-smokers or "social smokers" (defined as fewer than 5 cigarettes per week) willing to abstain from smoking for the duration of study

11. Willing to abstain from alcohol-containing, grapefruit-containing, or caffeine-containing foods or beverages

12. Able to read, understand and follow the study instructions

13. Agree to use of two effective methods of contraception

Exclusion Criteria

1. Allergy to onions or red wine
2. Strict vegetarians (i.e., subjects who do not eat meat, fish, fowl, or dairy)
3. Use of any non-study medication(s) during the study period other than those approved by the Investigator for treatment of an adverse event (AE)
4. Use of chemotherapy agents or history of cancer, other than non-metastatic non-melanoma skin cancer that has been completely excised, within five (5) years prior to the Screening visit
5. Use of any dietary aids or foods known to modulate drug metabolizing enzymes (e.g., St. John's Wort, grapefruit juice) within 4 days of randomization
6. History of bacterial or viral infection requiring treatment with antibiotics or antivirals within 30 days of randomization
7. Difficulty in swallowing oral medications
8. History of seizure disorder
9. Moderate to severe gastro-esophageal reflux disease
10. History of arrhythmia
11. Cognitive or psychiatric disorders, or any other condition that could interfere with compliance with study procedures and/or confinement in a clinical study unit
12. Baseline liver enzymes greater than the upper limit of normal
13. Baseline creatine phosphokinase (CPK) greater than 2.5x the upper limit of normal
14. History of drug or alcohol abuse
15. Use of any other investigational drug within 30 days of randomization or investigational biologic within 180 days of randomization
16. Use of over-the-counter (OTC) medications or nutraceuticals, excluding routine vitamins, within 14 days of randomization or 5 half-lives of the drug, whichever is longer
17. Use of prescription pharmaceuticals within 30 days of randomization
18. Donation and/or receipt of any blood or blood products within 90 days of randomization
19. Current gastrointestinal (GI), renal, hepatic, or coagulant disorder within 12 months of randomization
20. History of peptic or duodenal ulcer or GI bleed
21. Subjects with Gilbert's Syndrome
22. Subjects with positive drug or alcohol screen
23. Subject positive for hepatitis C antibody (HCV), hepatitis B surface antigen (HBsAg), or human immunodeficiency virus (HIV) antibody

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
A	LIM-0705	750 mg of LIM-0705 BID for 14 days. Up to 20 subjects.
B	Placebo	Placebo BID for 14 days. Up to 10 subjects.

Primary Outcome Measures

Name	Time	Method
To evaluate the effect of LIM-0705 on glucose metabolism, lipid metabolism and renal function in subjects with impaired glucose tolerance	approx. 1 month	* Assessment of glucose metabolism will be based on monitoring of overnight-fasting glucose levels and on performance of an Oral Glucose Tolerance Test (OGTT); * Assessment of lipid metabolism will be based on 12 hour-fasting lipid profiles (including LDL, HDL, total cholesterol, free fatty acids, and triglycerides); * Assessment of renal function will be performed by monitoring serum BUN and creatinine levels

Secondary Outcome Measures

Name	Time	Method
Incidence of treatment emergent adverse events and pharmacokinetics of LIM-0705 and its major metabolite	approx. 1 month	* To evaluate the incidence of treatment emergent adverse events; as well as changes in physical examination findings, vital signs, ECGs, and clinical laboratory tests (serum chemistry, hematology urinalysis, and coagulation); * To characterize the pharmacokinetics of LIM-0705 and its major metabolite