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A Study of XL092 as Single-Agent and Combination Therapy in Subjects With Solid Tumors

← catalyst calendar

NCT03845166 · readout in 12 d

Sponsored by Exelixis (industry) · EXEL — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
325actual
Sites
86
Countries
Australia, Belgium, Czechia +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
Start2019-03-20actualWhen the study began enrolling
Primary completion2026-08-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-05-31estimatedThe whole study's end, after follow-up
First posted2019-02-19actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-11-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Neoplasm Malignant
  • Renal Cell Carcinoma
  • Hormone Receptor Positive Breast Carcinoma
  • Metastatic Castration-resistant Prostate Cancer
  • Colorectal Cancer

Interventions

  • Drug: XL092
  • Drug: Atezolizumab — also filed as Tecentriq®
  • Drug: Avelumab — also filed as Bavencio®

Primary outcomes

what the primary-completion date above is the date OF
Dose-Escalation Stage: MTD/recommended dose for XL092
measured Up to 24 months
Cohort-Expansion Stage: Objective Response Rate (ORR)
measured Up to 24 months
Cohort-Expansion Stage (except Cohort H): Progression-Free Survival (PFS)
measured Up to 24 months
Cohort-Expansion Stage (Cohort H only): Overall Survival (OS)
measured Up to 24 months

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