NCT Number: NCT00330330
Safety, Tolerability, and Activity of ISIS 113715 in People With Type 2 Diabetes Mellitus Who Have Not Received Prior Treatment
The aim of this study is to evaluate the safety, tolerability, and pharmacokinetics of five ISIS 113715 intravenous dose cohorts in drug-naïve type 2 diabetics.
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Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
NZOZ Specjalistyczny Osrodek Internistyczno Diabetologiczny, Bialystok, Poland
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Type 2 Diabetes Mellitus of less than 5 years in duration
- Have never received hypoglycemic therapy
- Aged 18 to 65 years
- Fasting blood glucose between 130 and 220 mg/dL (7.2 to 12.2 mmol/L) for Cohorts A-D and between 140 and 220 mg/dL (7.8 to 12.2 mmol/L) for Cohort E
- HbA1c between 6.8 and 10.0% for Cohorts A-D and between 7.5 and 11.0% for Cohort E
- Body Mass index > 25 and < 35 kg m -2
Exclusion criteria
- Medication that may affect glucose homeostasis (e.g. systemic glucocorticoid) within one month of screening
- Clinically significant abnormalities in medical history or physical exam
- Clinically significant abnormalities on laboratory examination
- History of HIV infection
- Active infection requiring antiviral or antimicrobial therapy
- Malignancy (with the exception of basal or squamous cell carcinoma of the skin if adequately treated and no recurrence for > one year at the time of screening)
- Any other concurrent condition which, in the opinion of the Investigator, would preclude participation in or interfere with compliance
- Alcohol or drug abuse
- Undergoing or have undergone treatment with another investigational drug, biologic agent or device within 90 days of screening
- Abnormal serum creatinine concentration defined as > 1.5 mg/dL (132.6 micro mol/L) for males and > 1.2 mg/dL (106 micro mol/L) for females
- Medications that may affect coagulation (heparin, warfarin, etc.) with the exception of acetylsalicylic acid or non-steroidal anti-inflammatory agents.
- Allergy to sulfur-containing medications
Treatment and study plan
Primary outcomes
-
To evaluate the safety and tolerability of ISIS 113715
-
To evaluate the pharmacokinetic profile of ISIS 113715
-
To evaluate the pharmacologic activity of ISIS 113715
Sponsors and collaborators
Lead sponsor
Ionis Pharmaceuticals, Inc.
Industry
Registry information
Official study title
A Double-Blind, Placebo-Controlled, Dose-Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics, and Activity of ISIS 113715 in Patients With Type 2 Diabetes Mellitus Who Have Not Received Prior Therapy
Important dates
- Study start
- 2003
- Study completion
- 2006
- First posted
- May 26, 2006
- Registry last updated
- Feb 6, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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