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NCT06630247 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by Exelixis.

Terminated
Registry status
Phase 1
Development phase
9
Enrollment target

NCT06630247: Clinical Trial Phase 1 study, sponsored by Exelixis.

NCT06630247 is a Phase 1 study that was terminated before completion, run by Exelixis. The registered enrollment target is 9 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06630247, a Phase 1 study, was terminated before completion, sponsored by Exelixis.

TERMINATED
Registry status
Phase 1
Development phase
9 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG XL495
  • DRUG ADC cytotoxic agents

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2024-10-17
Est. Completion 2025-05-07
Phase Phase 1
Exelixis

48 total trials

Why NCT06630247 stopped before completion

NCT06630247 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 2 interventions - of which XL495 is the first listed.

NCT06630247 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06630247 about?

NCT06630247 is a clinical study titled "A Dose-escalation, Dose-finding, and Expansion Study of XL495 in Participants With Locally Advanced or Metastatic Solid Tumors". 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 availabl...

What is the current status of trial NCT06630247?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 9 participants. The study started on 2024-10-17. Estimated completion is 2025-05-07.

What interventions are being tested in trial NCT06630247?

The interventions under investigation include: XL495 (DRUG), ADC cytotoxic agents (DRUG).

Who is sponsoring clinical trial NCT06630247?

This trial is sponsored by Exelixis, which has 48 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06630247's enrollment target sits among peer trials

9 1955th of 2000 higher than 42 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06630247, the US trial registry maintained by the National Library of Medicine. NCT06630247 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.