Comparative Glucose Clamp Study of Wockhardt's Recombinant Insulin Analog Glargine(Glaritus) With Lantus in T1DM

Phase 1

Completed

• Conditions: Type1 Diabetes
• Interventions: Biological: Glargine

• Registration Number: NCT01357603
• Lead Sponsor: Wockhardt

Brief Summary

The aim of this trial is to demonstrate bioequivalence of Glaritus® to Lantus® with regard to its total and to its maximum serum insulin concentrations.

Detailed Description

The purpose of this study is to test for bioequivalence based on the pharmacokinetic parameter AUC INS-GLR 0-24h and on pharmacodynamic parameter AUC GIR 0-24h between the two long-acting insulin glargine formulations, Lantus® and Wockhardt's Glaritus® in subjects with type1 diabetes as well as assessing safety and local tolerability of the two insulin preparations.

Study Timeline

• Study First Submitted: 2011-05-12
• Study First Submitted QC: 2011-05-18
• Study First Posted: 2011-05-20
• Study Start: 2011-06
• Primary Completion: 2012-05
• Study Completion: 2012-08
• Status Verified: 2013-01
• Last Update Submitted: 2013-01-24
• Last Update Posted: 2013-01-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 111

Inclusion Criteria

1. Male or female subjects with type 1 diabetes ≥12 months.
2. HbA1c ≤9% by local laboratory analysis (one retest within a week is permitted with the result of the last test being conclusive).
3. Age ≥18 and ≤60 years.
4. Considered generally healthy upon completion of medical history, physical examination and biochemical investigations as judged by the Investigator.
5. Signed and dated informed consent obtained before any trial-related activities. (Trial-related activities are any procedure that would not have been performed during normal management of the subject).

Exclusion Criteria

1. Previous participation in this trial, or participation in other clinical trials within the last 30 days.
2. Pregnant, breast-feeding or the intention of becoming pregnant or not using adequate contraceptive measures (e.g. intrauterine device (IUD) that has been in place for at least 3 months, or sterilization, or the oral contraceptive pill, which should have been taken without difficulty for at least 3 months, an approved hormonal implant or double barrier method including male condoms used plus spermicide, diaphragm with spermicide plus male condom, cap with spermicide plus male condom).
3. History of any illness that, in the opinion of the Investigator, might confound the results of the trial or pose risk in administering the trial drug to the subject. In particular, subjects with significant cardiovascular disease, anemia (hemoglobin below the lower limit of normal) or hemoglobinopathy will not be allowed to enter the trial.
4. Cardiac problems defined as decompensated heart failure (New York Heart Association (NYHA) class III and IV) at any time and/or angina pectoris within the last 12 months and/or acute myocardial infarction at any time.
5. Clinically significant abnormal ECG at screening, as judged by the Investigator.
6. History of alcohol or drug abuse in the past five years.
7. Any positive reaction of drug abuse.
8. Hepatitis B or C or HIV positive.
9. Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.
10. History of multiple and/or severe allergies to drugs or foods or a history of severe anaphylactic reaction.
11. Regular cigarette smoker, defined as smoking >1 pack/day and unable to refrain from smoking during the in house period.
12. Known or suspected allergy to trial product or related products.
13. Any disease or condition that, in the opinion of the Investigator, would represent an unacceptable risk for the subject's safety.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Glaritus arm	Glargine	Insulin glargine (Glaritus: 100 U/ml), Penfill® cartridges 3.0ml
Lantus arm	Glargine	Insulin glargine (Lantus: 100 U/ml), Penfill® cartridges 3.0ml

Primary Outcome Measures

Name	Time	Method
Bioequivalence based on Pharmacokinetic parameter:AUC INS-GLR 0-24h.	over 24hrs post dose
Bioequivalence based on Pharmacodynamic parameter: AUC GIR 0-24hrs	over 24hrs post dose
Pharmacokinetic Parameters: Maximum concentration (Cmax)	over 24hrs post dose

Secondary Outcome Measures

Name	Time	Method
Safety parameters	till 24 hrs post-dose	Number of AE's, SAE's, Hypoglycemic events and local tolerability
Pharmacodynamic parameters: Area under curve glucose infusion rate from 0-24hrs	over 24hrs post dose	AUC GIR 0-12h,AUC GIR 12-24h,AUC GIR 0-24h
Pharmacokinetic parameter: Area under curve from 0-24hrs	over 24hrs post dose	AUC INS-GLR 0-12hrs, AUC INS-GLR 12-24hrs,AUC INS-GLR 0-24hrs
Pharmacokinetic Parameters: tmax and t1/2	over 24hrs post dose
Pharmacodynamic parameter: GIR max and tGIR max	over 24hrs post dose

Trial Locations

Locations (1)

Profil Institute for clinical Research; 🇺🇸 Chula Vista, California, United States