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A Study to Evaluate LY3537021 for the Treatment of Nausea and Vomiting Caused by Chemotherapy in Adults With Cancer

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NCT07169851 · readout ≤ 133 d

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
204estimated
Sites
67
Countries
Australia, China, France +7

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-11-28actualWhen the study began enrolling
Primary completionDec 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionFeb 2027estimatedThe whole study's end, after follow-up
First posted2025-09-12actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Nausea
  • Vomiting
  • Drug-Related Side Effects and Adverse Reactions
  • Neoplasms

Interventions

  • Drug: LY3537021
  • Drug: Placebo
  • Drug: Standard of Care Antiemetic Therapies
  • Drug: Background Chemotherapy

Primary outcome

what the primary-completion date above is the date OF
Proportion of Participants with a Complete Response (CR) in the Delayed Phase of CINV
measured 24 to 120 hours after first chemotherapy infusion

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