Viewing Study NCT06297603



Ignite Creation Date: 2024-05-06 @ 8:13 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06297603
Status: RECRUITING
Last Update Posted: 2024-06-20
First Post: 2024-03-01

Brief Title: Effect of Retatrutide Compared With Placebo in Participants With Type 2 Diabetes and Moderate or Severe Renal Impairment With Inadequate Glycemic Control on Basal Insulin With or Without Metformin andor SGLT2 Inhibitor TRANSCEND-T2D-3
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: A Phase 3 Randomized Multicenter Double-Blind Study to Investigate the Efficacy and Safety of Retatrutide Once Weekly Compared With Placebo in Adult Participants With Type 2 Diabetes Moderate or Severe Renal Impairment With Inadequate Glycemic Control on Basal Insulin With or Without Metformin andor SGLT2 Inhibitor
Status: RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to investigate the efficacy and safety of retatrutide compared with placebo in participants with Type 2 Diabetes and renal impairment with inadequate glycemic control on basal insulin alone or a combination of basal insulin with or without metformin andor sodium-glucose cotransporter-2 SGLT2 inhibitor The study will last about 14 months and may include up to 22 visits
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
J1I-MC-GZQA OTHER Eli Lilly and Company None