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A Study of LOXO-783 in Patients With Breast Cancer/Other Solid Tumors

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NCT05307705 · readout ≤ 134 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
260estimated
Sites
50
Countries
Australia, Belgium, Canada +9

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
Start2022-05-11actualWhen the study began enrolling
Primary completionDec 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2026estimatedThe whole study's end, after follow-up
First posted2022-04-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-07actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Breast Cancer

Interventions

  • Drug: LOXO-783 — also filed as LY3849524
  • Drug: Fulvestrant
  • Drug: Imlunestrant — also filed as LY3484356
  • Drug: Abemaciclib — also filed as LY2835219
  • Drug: Anastrozole, Exemestane, or Letrozole
  • Drug: Paclitaxel

Primary outcomes

what the primary-completion date above is the date OF
Phase 1 a: To determine the maximum tolerated dose/recommended phase 2 dose (MTD/RP2D) of LOXO-783: Number of patients with dose-limiting toxicities (DLTs)
measured During the first 28-day cycle of LOXO-783 treatment
Phase 1 a: To determine the MTD/RP2D of LOXO-783: Number of patients with DLT-equivalent toxicities
measured During the first 28-day cycle of LOXO-783 treatment

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