A Study to Assess the Safety of Single Doses of GSK189075 in Subjects With Type 1 Diabetes Mellitus
Launched by GLAXOSMITHKLINE · Dec 14, 2007
Trial Information
Current as of June 05, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Adult male/female, 18 to 55 years old
- • Diagnosis of type 1 diabetes mellitus for at least 6 months; and using a continuous insulin pump
- • Willing and able to follow all study-related instructions provided by the site staff.
- • Willing to provide signed informed consent.
- Exclusion Criteria:
- • Pregnant or a nursing female.
- • Have a past or current disease such as heart, liver, kidney, blood, brain, or other disease.
- • Have HIV or hepatitis, or have alcohol or drugs in your system at the screening visit.
- • Have a history of alcohol abuse or have an eating disorder
- • Have been in another research study in the last month or have taken certain medications in the 1 week before study drug would be taken.
About Glaxosmithkline
GlaxoSmithKline (GSK) is a global healthcare company dedicated to improving the quality of human life by enabling people to do more, feel better, and live longer. With a strong focus on research and development, GSK specializes in pharmaceuticals, vaccines, and consumer health products. The company is committed to advancing innovative therapies and preventive measures across various therapeutic areas, including respiratory, oncology, immunology, and infectious diseases. GSK's collaborative approach and rigorous clinical trial processes underscore its dedication to delivering safe and effective healthcare solutions that meet the needs of patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Diego, California, United States
San Diego, California, United States
Patients applied
Trial Officials
GSK Clinical Trials
Study Director
GlaxoSmithKline
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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