Glulisine Pre- and Postmeal

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-12-31

Study Completion Date

2002-03-31

Brief Summary

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To investigate in type 1 diabetic patients the glucodynamic response to HMR1964 insulin and RHI (HOE31HPR100) injected subcutaneously before and after a standard meal

Detailed Description

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Conditions

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Diabetes Mellitus Type 1

Keywords

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Insulin glulisine Diabetes mellitus Type 1 Postprandial Period Pharmacokinetics Glucodynamics

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Insulin glulisine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Type 1 diabetes mellitus

Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Principal Investigators

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Klaus Rave, Dr.

Role: PRINCIPAL_INVESTIGATOR

Profil Institut für Stoffwechselforschung GmbH, Neuss, Germany

Other Identifiers

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HMR1964

Identifier Type: -

Identifier Source: secondary_id

HMR1964A/1008