Phase 1 Study of BHT-3021 in Subjects With Type 1 Diabetes Mellitus

PHASE1CompletedINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

October 31, 2006

Primary Completion Date

May 31, 2011

Study Completion Date

May 31, 2011

Conditions
DiabetesHypoglycemia
Interventions
DRUG

BHT-3021

Evaluation of up to four dose levels will be given in weekly IM injections for 12 weeks.

DRUG

BHT-Placebo

Evaluation of up to four dose levels will be given in weekly IM injections for 12 weeks.

Trial Locations (18)

3050

Royal Melbourne Hospital, Parkville

Eastern Clinical Research Unit, Ringwood East

4021

Peninsula Clinical Research Centre, Kippa-Ring

6160

Fremantle Hospital, Fremantle

20003

MedStar Research Institute, Washington D.C.

33136

University of Miami, Miller School of Medicine, Diabetes Research Institute, Miami

33414

Private Practice, Wellington

35294

University of Alabama at Birmingham School of Medicine, Birmingham

68131

Creighton Diabetes Center, Omaha

78229

Diabetes and Glandular Disease Center, San Antonio

80045

Barbara Davis Center for Childhood Diabetes, Aurora

80209

Private Practice, Denver

93720

Valley Research, Fresno

98101-2795

Benaroya Research Institute at Virginia Mason, Seattle

Private Bag 93311

Middlemore Hospital, Otahuhu

Private Bag 4710

Christchurch Hospital, Christchurch

Private bag 3200

Waikato Regional Diabetes Service, Hamilton

Private Bag 7902

The Diabetes Centre, Newtown

Sponsors
All Listed Sponsors
lead

Bayhill Therapeutics

INDUSTRY