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Safety, Tolerability, and Activity of ISIS 113715 in People With Type 2 Diabetes Mellitus Being Treated With Sulfonylurea

Primary Purpose

Type 2 Diabetes Mellitus

Status
Withdrawn
Phase
Phase 2
Locations
Israel
Study Type
Interventional
Intervention
ISIS 113715
Sponsored by
Ionis Pharmaceuticals, Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes Mellitus focused on measuring Fasting plasma glucose, HbA1c, Oral antidiabetic agent(s)

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Male or female (post-menopausal and/or surgically sterile) Aged 18 to 70 years Diagnosed with type 2 diabetes mellitus of eight years or less in duration Being treated with OAD at stable maximum doses [defined as at least 10 mg/day glibenclamide (preferred), or 20 mg/day glipizide, with or without at least 1,500 mg/day metformin] for at least three months prior to screening Having fasting plasma glucose levels of 150-270 mg/dL and HbA1c levels of 7.5-11.0% Exclusion Criteria: Greater than 3 severe hypoglycemic episodes within six months of screen Pregnant, breastfeeding, or intends to become pregnant Clinical signs or symptoms of liver disease, acute, or chronic hepatitis, or ALT greater than the upper limit of normal Positive hepatitis B surface antigen, hepatitis C antibody, or HIV test Patients with history of renal transplantation or renal dialysis or microalbuminuria defined as urine albumin > 200 mg/day History of insulin use within three months of screen History of diabetic ketoacidosis Treatment with any thiazolidinedione (e.g., rosiglitazone) within three months of screen History of lactic acidosis while on metformin therapy Complications of diabetes (e.g., neuropathy, nephropathy, and retinopathy) Clinically significant and currently active diseases Clinical significant abnormalities in medical history, physical examination, or laboratory examination

Sites / Locations

  • Soroka Medical Center
  • Rambam Medical Center
  • Western Galilee Medical Center - Nahariya
  • Kaplan Medical Center
  • ZIV Hospital

Outcomes

Primary Outcome Measures

Evaluate the safety, tolerability, and pharmacokinetics of two ISIS 113715 subcutaneous dosages in combination with OAD versus OAD + placebo.
Examine the effect of treatment with 15 and 30 mg/day ISIS 113715 on fasting plasma glucose and HbA1c.
Evaluate the effects of ISIS 113715 on insulin sensitivity, B-cell function, proinsulin/insulin ratio, fasting insulin, C-peptide and proinsulin.

Secondary Outcome Measures

Full Information

First Posted
May 16, 2006
Last Updated
December 1, 2022
Sponsor
Ionis Pharmaceuticals, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00327626
Brief Title
Safety, Tolerability, and Activity of ISIS 113715 in People With Type 2 Diabetes Mellitus Being Treated With Sulfonylurea
Official Title
A Phase 2, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Activity of ISIS 113715 Administered Daily in Patients With Type 2 Diabetes Mellitus Being Treated With Sulfonylurea
Study Type
Interventional

2. Study Status

Record Verification Date
May 2007
Overall Recruitment Status
Withdrawn
Why Stopped
study was never started due to regional geopolitical conflict
Study Start Date
May 1, 2006 (Actual)
Primary Completion Date
February 1, 2007 (Actual)
Study Completion Date
March 1, 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ionis Pharmaceuticals, Inc.

4. Oversight

5. Study Description

Brief Summary
The aim of this study is to evaluate the safety, tolerability, and pharmacokinetics of two ISIS 113715 subcutaneous doses (15 mg and 30 mg/day) in combination with oral antidiabetic agents (OAD) versus OAD + placebo in patients with inadequately controlled type 2 diabetes, despite ongoing maximal treatment with OAD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus
Keywords
Fasting plasma glucose, HbA1c, Oral antidiabetic agent(s)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
ISIS 113715
Primary Outcome Measure Information:
Title
Evaluate the safety, tolerability, and pharmacokinetics of two ISIS 113715 subcutaneous dosages in combination with OAD versus OAD + placebo.
Title
Examine the effect of treatment with 15 and 30 mg/day ISIS 113715 on fasting plasma glucose and HbA1c.
Title
Evaluate the effects of ISIS 113715 on insulin sensitivity, B-cell function, proinsulin/insulin ratio, fasting insulin, C-peptide and proinsulin.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female (post-menopausal and/or surgically sterile) Aged 18 to 70 years Diagnosed with type 2 diabetes mellitus of eight years or less in duration Being treated with OAD at stable maximum doses [defined as at least 10 mg/day glibenclamide (preferred), or 20 mg/day glipizide, with or without at least 1,500 mg/day metformin] for at least three months prior to screening Having fasting plasma glucose levels of 150-270 mg/dL and HbA1c levels of 7.5-11.0% Exclusion Criteria: Greater than 3 severe hypoglycemic episodes within six months of screen Pregnant, breastfeeding, or intends to become pregnant Clinical signs or symptoms of liver disease, acute, or chronic hepatitis, or ALT greater than the upper limit of normal Positive hepatitis B surface antigen, hepatitis C antibody, or HIV test Patients with history of renal transplantation or renal dialysis or microalbuminuria defined as urine albumin > 200 mg/day History of insulin use within three months of screen History of diabetic ketoacidosis Treatment with any thiazolidinedione (e.g., rosiglitazone) within three months of screen History of lactic acidosis while on metformin therapy Complications of diabetes (e.g., neuropathy, nephropathy, and retinopathy) Clinically significant and currently active diseases Clinical significant abnormalities in medical history, physical examination, or laboratory examination
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark K Wedel, MD, JD, FACP
Organizational Affiliation
Ionis Pharmaceuticals, Inc.
Official's Role
Study Director
Facility Information:
Facility Name
Soroka Medical Center
City
BeEr-Sheva
ZIP/Postal Code
84101
Country
Israel
Facility Name
Rambam Medical Center
City
Haifa
ZIP/Postal Code
31096
Country
Israel
Facility Name
Western Galilee Medical Center - Nahariya
City
Nahariya
ZIP/Postal Code
22100
Country
Israel
Facility Name
Kaplan Medical Center
City
Rehovot
ZIP/Postal Code
76100
Country
Israel
Facility Name
ZIV Hospital
City
Safed
ZIP/Postal Code
13100
Country
Israel

12. IPD Sharing Statement

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Safety, Tolerability, and Activity of ISIS 113715 in People With Type 2 Diabetes Mellitus Being Treated With Sulfonylurea

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