Anti-CD3 mAb Treatment of Recent Onset Type 1 Diabetes

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborators:
Juvenile Diabetes Research Foundation
Information provided by (Responsible Party):
Kevan Herold, Yale University
ClinicalTrials.gov Identifier:
NCT00378508
First received: September 18, 2006
Last updated: October 31, 2012
Last verified: October 2012
Results First Received: September 4, 2012  
Study Type: Interventional
Study Design: Allocation: Randomized;   Endpoint Classification: Safety/Efficacy Study;   Intervention Model: Parallel Assignment;   Masking: Double Blind (Subject, Caregiver, Investigator);   Primary Purpose: Treatment
Condition: Type 1 Diabetes Mellitus
Interventions: Drug: mAb hOKT3gamma1(Ala-Ala), Teplizumab
Drug: Placebo Arm

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
Subjects were recruited from 4 clinical sites and were eligible if they were between the ages of 8-30 and diagnosed with Type 1 Diabetes for at least 4 months, but not more than 12 months prior to enrollment.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
No text entered.

Reporting Groups
  Description
Saline Infusions (Placebo) The course of normal saline infusion comprises daily doses of 51 µg/m2, 103 µg/m2, 207 µg/m2, 413 µg/m2, and 10 of 826 µg/m2 over a 14 day treatment period.
Teplizumab Infusion (Active) The course of teplizumab infusion comprises daily doses of 51 µg/m2, 103 µg/m2, 207 µg/m2, 413 µg/m2, and 10 of 826 µg/m2 over a 14 day treatment period.

Participant Flow:   Overall Study
    Saline Infusions (Placebo)     Teplizumab Infusion (Active)  
STARTED     29     34  
Randomized     29     34  
Received Intervention/Placebo     28     31  
COMPLETED     27     31  
NOT COMPLETED     2     3  
Withdrawal by Subject                 1                 3  
Lost to Follow-up                 1                 0  



  Baseline Characteristics
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Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
No text entered.

Reporting Groups
  Description
Saline Infusions (Placebo) The course of normal saline infusion comprises daily doses of 51 µg/m2, 103 µg/m2, 207 µg/m2, 413 µg/m2, and 10 of 826 µg/m2 over a 14 day treatment period.
Teplizumab Infusions (Active) The course of teplizumab infusion comprises daily doses of 51 µg/m2, 103 µg/m2, 207 µg/m2, 413 µg/m2, and 10 of 826 µg/m2 over a 14 day treatment period.
Total Total of all reporting groups

Baseline Measures
    Saline Infusions (Placebo)     Teplizumab Infusions (Active)     Total  
Number of Participants  
[units: participants]
  27     31     58  
Age, Customized  
[units: participants]
     
<15 years     20     18     38  
>=15 years     7     13     20  
Gender, Customized  
[units: participants]
     
Female     10     15     25  
Male     17     16     33  



  Outcome Measures
  Show All Outcome Measures

1.  Primary:   C-peptide Area Under the Curve (AUC) Response to a Mixed Meal Tolerance Test (MMTT) at 12 Months   [ Time Frame: At month 12 post-treatment ]

2.  Primary:   C-peptide Area Under the Curve (AUC) Response to a Mixed Meal Tolerance Test (MMTT) at Baseline   [ Time Frame: At Baseline (before treatment) ]

3.  Secondary:   Hemoglobin A1c   [ Time Frame: At 12 months post-treatment ]

4.  Secondary:   Average Insulin Use Over 12 Months   [ Time Frame: After 12 months post-treatment ]

5.  Secondary:   Baseline Insulin Use   [ Time Frame: At baseline (before treatment) ]

6.  Secondary:   Baseline Hemoglobin A1c   [ Time Frame: At baseline (before treatment) ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
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Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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  More Information
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Certain Agreements:  
All Principal Investigators ARE employed by the organization sponsoring the study.


Results Point of Contact:  
Name/Title: Kevan Herold, MD
Organization: Yale University
phone: 203-785-6507
e-mail: Kevan.Herold@yale.edu


Publications:
Publications automatically indexed to this study:

Responsible Party: Kevan Herold, Yale University
ClinicalTrials.gov Identifier: NCT00378508     History of Changes
Other Study ID Numbers: Delay-Study 5, R01DK57846
Study First Received: September 18, 2006
Results First Received: September 4, 2012
Last Updated: October 31, 2012
Health Authority: United States: Food and Drug Administration