Authorised Therapeutic exploratory (Phase II) Type 2 Diabetes

A Study of LY3457263 Compared to Placebo in Participants with Type 2 Diabetes on a Stable Dose of Semaglutide or Tirzepatide

EU CTIS ID: 2024-520328-27-00

What this study is testing

To compare HbA1c lowering efficacy of LY3457263 versus placebo at 24 weeks

  • Therapeutic exploratory (Phase II)

A plain-language read of the study's public EU CTIS listing. The study team confirms the details.

Who can take part

You may be able to join if

  • Have type 2 diabetes
  • Have overweight or obesity
  • Have a stable body weight for three months prior to screening
  • Be on a stable dose of injectable semaglutide or injectable tirzepatide for at least three months

You likely can't join if

  • Have type 1 diabetes
  • Have taken any medications or alternative remedies for weight loss within three months prior to screening

The study team makes the final eligibility decision.

Where it's taking place

  • United States
  • Canada
  • United Kingdom

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18-64 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include United States; Canada; United Kingdom. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.