Overview
A Multiple Dose Study of LY3209590 in Participants With Type 2 Diabetes
Status:
Active, not recruiting
Active, not recruiting
Trial end date:
2024-07-20
2024-07-20
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to measure the activity and insulin time action of LY3209590 at steady state in participants with type 2 diabetes mellitus. The total study duration is approximately 182 days.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Eli Lilly and Company
Criteria
Inclusion Criteria:- Participants with Type 2 Diabetes (T2DM).
- Participants who are insulin naive or receiving basal insulin [NPH (neutral protamine
Hagedorn) once or twice daily, once-daily insulin glargine U100 or U300, once-daily
insulin degludec, or insulin detemir once or twice daily] for fewer than 5 years prior
to screening.
- Have glycated hemoglobin (HbA1c) of ≥7.0 percent (%) to ≤9.5%, HbA1c of ≥6.5% to ≤9.5%
for participants on treatment with sulfonylureas and/or Sodium-Glucose Transport
Protein 2 inhibitors who require washout.
- Have a body mass index between 27 and 40 kilograms per meter square.
- Male or female participants who are willing to comply with the contraception
requirements consistent with local regulations.
- Be willing to allow blood sample collection, reliable and to be available for the
duration of the study as required for the study protocol.
Exclusion Criteria:
- Have known or suspected allergic reactions to study drugs, related compounds,
excipients, and devices used in the study.
- Have a specific type of diabetes other than T2DM.
- Have known hemoglobinopathy, hemolytic anemia or sickle cell anemia, or any other
traits of hemoglobin abnormalities known to interfere with the measurement of HbA1c.
- Participants with a history of kidney complications.