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No longer availableNCT01945164Updated Oct 21, 2014

XL999 Administered Intravenously to a Subject With Advanced Malignancies

An expanded access record providing XL999 in Advanced Malignancy, sponsored by John Sarantopoulos. No longer available at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-10-21.

Sponsored by John Sarantopoulos · Expanded access

Study type
Expanded access
Ages
18 Years and older
Sex
All
01

Study summary

Cancer is a worldwide clinical and economic problem. Conventional approaches to treating cancer include surgery, radiotherapy, and cytotoxic chemotherapy as single modalities or as combined therapies. Recently, targeted therapies including antibodies and small molecule inhibitors have also demonstrated clinical benefit. It is now possible to study different genetic lesions involved in cancer types due to advances in genomic methodologies. The investigational drug in this study, XL999 inhibits multiple receptor tyrosine kinases, including VEGF receptor (VEGFR2/KDR), platelet derived growth factor receptors (PDGFRβ), fms-like tyrosine kinase receptor 3 (FLT3), fibroblast growth factor receptors (FGFR1, FGFR3), RET, and KIT, and thus, interferes with multiple cellular processes simultaneously and will likely have effects on the integrity of tumor neovasculature and angiogenesis. Together with the ability to induce a novel cell cycle arrest, the spectrum of activities that XL999 exhibits may reduce both tumor cell proliferation and angiogenesis in the clinic.

The rationale and purpose of this maintenance study is to allow a subject receiving clinical benefit from XL999 to continue treatment.

02

Conditions studied

  • Advanced Malignancy

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Keywords

  • XL999
  • Advanced Malignancy
03

In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,486 are open to participants now.

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Lead sponsor

This is the only study on the registry with John Sarantopoulos as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • The subject is eligible to continue to receive XL999 in the absence of progressive disease and unacceptable XL999-related toxicity.

Exclusion criteria

Exclusion Criteria:

  • Progressive disease.
05

Access details

Study type
Expanded access

Available treatment

  • DrugXL999

    The treatment will consist of 4-week cycles in which the subject will receive XL999 administered as a 4-hour IV infusion every other week. The subject will continue to receive 4-week cycles of XL999 in the absence of progressive disease, unacceptable drug-related toxicity, and as long as the drug is available.

06

Where to request access

1 site
  • Cancer Therapy and Research Center at UTHSCSA
    San Antonio, Texas 78229, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 21, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT01945164
Lead sponsor
John Sarantopoulos
Responsible party
John Sarantopoulos (Principal Investigator, The University of Texas Health Science Center at San Antonio) — Sponsor-investigator
First posted
Sep 18, 2013
Start date
Apr 2010
Primary completion
Jun 2012
Completion
Jun 2012
Last update
Oct 21, 2014

Study contacts

John Sarantopoulos, MD
principal investigator · University of Texas Health Science Center San Antonio

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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