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Study of XB010 in Subjects With Solid Tumors

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NCT06545331 · readout in 96 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
396estimated
Sites
20
Countries
United Kingdom, United States

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
Start2024-08-06actualWhen the study began enrolling
Primary completion2026-11-23estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-10-20estimatedThe whole study's end, after follow-up
First posted2024-08-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Locally Advanced or Metastatic Solid Tumors
  • Esophageal Squamous Cell Cancer
  • Head and Neck Squamous Cell Cancer
  • NSCLC (Non-small Cell Lung Cancer)
  • Hormone-receptor-positive Breast Cancer
  • Triple Negative Breast Cancer (TNBC)

Interventions

  • Drug: XB010
  • Drug: Pembrolizumab

Primary outcomes

what the primary-completion date above is the date OF
Dose-Escalation Stage: Maximum tolerated dose (MTD) and/or Recommended dose(s) for Expansion [RDE(s)] for XB010
measured 18 months
Dose-Escalation Stage: Safety of XB010
measured 18 months
Dose-Escalation Stage: Duration of exposure of XB010 [Tolerability]
measured 18 months
Dose-Escalation Stage: Dose intensity of XB010 [Tolerability]
measured 18 months
Cohort-Expansion Stage: Preliminary antitumor activity of XB010
measured 24 months

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