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NCT00336765 · ClinicalTrials.gov registry record · Phase 1

Study of XL647 Administered Orally Daily to Patients With Solid Tumors

A Phase 1 study of Cancer, sponsored by Kadmon Corporation.

Completed
Registry status
Phase 1
Development phase
31
Enrollment target
2
Study locations

NCT00336765: Completed Phase 1 study of Cancer, sponsored by Kadmon Corporation.

NCT00336765 is a Phase 1 study of Cancer that has completed, run by Kadmon Corporation. The registered enrollment target is 31 participants, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00336765, a Phase 1 study of Cancer, has completed, sponsored by Kadmon Corporation.

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to assess the safety and tolerability of the multiple receptor tyrosine kinase (RTK) inhibitor (including EGFR, VEGFR2, ErbB2, and EphB4) XL647 when given orally daily to adults with advanced solid tumors.

Conditions Studied

Interventions

  • DRUG XL647

Study Locations (2)

California

  • Stanford University Medical Center - Stanford

Minnesota

  • Mayo Clinic - Rochester

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2006-07
Est. Completion 2010-09
Phase Phase 1
Kadmon Corporation

15 total trials

What the finished NCT00336765 record still lists

NCT00336765 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 3,491-participant average among 615 other Cancer trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Cancer appearing as the primary indexed condition, and to 1 intervention - of which XL647 is the first listed.

NCT00336765 reports a single indexed study location in California, Minnesota.

Frequently Asked Questions

What is clinical trial NCT00336765 about?

NCT00336765 is a clinical study titled "Study of XL647 Administered Orally Daily to Patients With Solid Tumors". The purpose of this study is to assess the safety and tolerability of the multiple receptor tyrosine kinase (RTK) inhibitor (including EGFR, VEGFR2, ErbB2, and EphB4) XL647 when given orally daily to adults with advanced solid tumors.

What is the current status of trial NCT00336765?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2006-07. Estimated completion is 2010-09.

What conditions does trial NCT00336765 study?

This clinical trial studies the following conditions: Cancer.

What interventions are being tested in trial NCT00336765?

The interventions under investigation include: XL647 (DRUG).

Who is sponsoring clinical trial NCT00336765?

This trial is sponsored by Kadmon Corporation, which has 15 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00336765 being conducted?

This trial has 2 study locations across California, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00336765's enrollment target sits among peer trials

31 499th of 615 higher than 115 of 615 other Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cancer 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 NCT00336765, the US trial registry maintained by the National Library of Medicine. NCT00336765 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.