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NCT06630247

A Dose-escalation, Dose-finding, and Expansion Study of XL495 in Participants With Locally Advanced or Metastatic Solid Tumors

Terminated Phase 1 Last updated 25 June 2025
What this trial tests

Phase 1 trial testing XL495 in Solid Cancers in 9 participants. Terminated before completion.

Timeline
17 October 2024
Primary endpoint
7 May 2025
7 May 2025

Quick facts

Lead sponsorExelixis
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment9
Start date17 October 2024
Primary completion7 May 2025
Estimated completion7 May 2025
Sites10 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Exelixis — full company profile →

Who can join

18 and older, any sex, with Solid Cancers or Solid Tumor Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this study is to obtain safety, tolerability, PK, and preliminary clinical antitumor activity for XL495 as a single agent and in combination with select cytotoxic agents in participants with locally advanced or metastatic tumors for whom life-prolonging therapies do not exist or available therapies are intolerable/no longer effective.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Solid Cancers

Currently open trials in the same condition.

Other Exelixis trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06630247.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing