A Study to Evaluate the Efficacy and Safety of CJC-1134-PC in Patients With Type 2 Diabetes Who Are Currently on Metformin Monotherapy

NCT ID: NCT00674466

Last Updated: 2017-06-02

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-03-31

Study Completion Date

2008-11-30

Brief Summary

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This is a multicenter, randomized, placebo-controlled, double-blind, Phase II study. The objective of this study is to evaluate the efficacy and safety of 12 weeks of treatment with CJC-1134-PC in patients who are currently on metformin monotherapy.

Detailed Description

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Conditions

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Type 2 Diabetes Mellitus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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1

Twice-a-week dose of 1.5 mg CJC-1134-PC

Group Type EXPERIMENTAL

1.5 mg or 2.0 mg CJC-1134-PC

Intervention Type DRUG

twice-a-week

2

Twice-a-week dose of 1.5 mg CJC-1134-PC for 4 weeks, then once-a-week dose of 2.0 mg CJC-1134-PC plus mid-week dosing of placebo

Group Type EXPERIMENTAL

1.5 mg or 2.0 mg CJC-1134-PC

Intervention Type DRUG

twice-a-week

3

Twice-a-week placebo for CJC-1134-PC

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

twice-a-week

Interventions

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1.5 mg or 2.0 mg CJC-1134-PC

twice-a-week

Intervention Type DRUG

Placebo

twice-a-week

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* BMI: 27 to 45 kg/m2
* Stable Type 2 diabetes mellitus for at least 3 months, as defined by the Investigator
* Stable life-style, i.e. diet \& physical activity, as determined by the Investigator
* Stable metformin daily dose ≥1000 mg for at least 3 months
* Glycosylated hemoglobin (HbA1c) at screening ≥ 7.1% and ≤ 11%
Minimum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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ConjuChem

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Maggie Wang, MD

Role: STUDY_DIRECTOR

ConjuChem Biotechnologies Inc.

Locations

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Maggie Wang

Montreal, Quebec, Canada

Site Status

Countries

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Canada

Other Identifiers

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DM200-102

Identifier Type: -

Identifier Source: org_study_id

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