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COMPLETED Phase 1

PTC299 in Treating Young Patients With Refractory or Recurrent Primary Central Nervous System Tumors

NCT01158300 · View on ClinicalTrials.gov ↗

Study Summary

RATIONALE: PTC299 may stop the growth of tumor cells by blocking blood flow to the tumor. PURPOSE: This phase I trial is studying the side effects and the best dose of PTC299 in treating young patients with recurrent or refractory primary central nervous system tumors.

Interventions

  • DRUG VEGF inhibitor PTC299

Study Locations (8)

Pennsylvania

  • Children's Hospital of Philadelphia — Philadelphia
  • Children's Hospital of Pittsburgh — Pittsburgh

California

  • UCSF Cancer Center and Cancer Research Institute — San Francisco

District of Columbia

  • Children's National Medical Center — Washington D.C.

Illinois

  • Children's Memorial Hospital - Chicago — Chicago

North Carolina

  • Duke Comprehensive Cancer Center — Durham

Tennessee

  • St. Jude Children's Research Hospital — Memphis

Texas

  • Texas Children's Cancer Center and Hematology Service at Texas Children's Hospital — Houston

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2010-11
Est. Completion 2015-01
Phase Phase 1

Sponsor

Pediatric Brain Tumor Consortium

8 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01158300

The ClinicalTrials.gov registry entry for NCT01158300 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pediatric Brain Tumor Consortium, which has 8 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Brain and Central Nervous System Tumors appearing as the primary indexed condition, and to 1 intervention — of which VEGF inhibitor PTC299 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01158300 reports 8 study locations spanning 7 distinct geographic areas — top geographies include Pennsylvania, California, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01158300 about?

NCT01158300 is a clinical study titled "PTC299 in Treating Young Patients With Refractory or Recurrent Primary Central Nervous System Tumors". RATIONALE: PTC299 may stop the growth of tumor cells by blocking blood flow to the tumor. PURPOSE: This phase I trial is studying the side effects and the best dose of PTC299 in treating young patients with recurrent or refractory primary central nervous system tumors.

What is the current status of trial NCT01158300?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2010-11. Estimated completion is 2015-01.

What conditions does trial NCT01158300 study?

This clinical trial studies the following conditions: Brain and Central Nervous System Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01158300?

The interventions under investigation include: VEGF inhibitor PTC299 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01158300?

This trial is sponsored by Pediatric Brain Tumor Consortium, which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01158300 being conducted?

This trial has 8 study locations across California, District of Columbia, Illinois, North Carolina, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial