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COMPLETED Phase 1

Trebananib in Treating Younger Patients With Relapsed or Refractory Solid Tumors, Including Central Nervous System Tumors

NCT01538095 · View on ClinicalTrials.gov ↗

Study Summary

This phase I trial studies the side effects and best dose of trebananib in treating patients with solid tumors that has returned after a period of improvement or does not respond to treatment, including central nervous system tumors. Trebananib may stop the growth of tumor cells by blocking blood flow to the tumor.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • PROCEDURE Dynamic Contrast-Enhanced Magnetic Resonance Imaging
  • OTHER Pharmacological Study
  • BIOLOGICAL Trebananib

Study Locations (20)

Pennsylvania

  • Children's Hospital of Philadelphia — Philadelphia
  • Childrens Oncology Group — Philadelphia
  • Children's Hospital of Pittsburgh of UPMC — Pittsburgh

Alabama

  • Children's Hospital of Alabama — Birmingham
  • University of Alabama at Birmingham Cancer Center — Birmingham

California

  • Children's Hospital of Orange County — Orange
  • UCSF Medical Center-Parnassus — San Francisco

District of Columbia

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

Georgia

  • Children's Healthcare of Atlanta - Egleston — Atlanta

Illinois

  • Lurie Children's Hospital-Chicago — Chicago

Indiana

  • Riley Hospital for Children — Indianapolis

Michigan

  • C S Mott Children's Hospital — Ann Arbor

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2012-02
Est. Completion 2016-04
Phase Phase 1

Sponsor

National Cancer Institute (NCI)

2,390 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01538095

The ClinicalTrials.gov registry entry for NCT01538095 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 37 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Cancer Institute (NCI), which has 2,390 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Solid Neoplasm appearing as the primary indexed condition, and to 4 interventions — of which Laboratory Biomarker Analysis 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: NCT01538095 reports 20 study locations spanning 16 distinct geographic areas — top geographies include Pennsylvania, Alabama, California. 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 NCT01538095 about?

NCT01538095 is a clinical study titled "Trebananib in Treating Younger Patients With Relapsed or Refractory Solid Tumors, Including Central Nervous System Tumors". This phase I trial studies the side effects and best dose of trebananib in treating patients with solid tumors that has returned after a period of improvement or does not respond to treatment, including central nervous system tumors. Trebananib may stop the growth of tumor cells by blocking blood fl...

What is the current status of trial NCT01538095?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2012-02. Estimated completion is 2016-04.

What conditions does trial NCT01538095 study?

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

What interventions are being tested in trial NCT01538095?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Dynamic Contrast-Enhanced Magnetic Resonance Imaging (PROCEDURE), Pharmacological Study (OTHER), Trebananib (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01538095?

This trial is sponsored by National Cancer Institute (NCI), which has 2,390 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01538095 being conducted?

This trial has 20 study locations across Alabama, California, District of Columbia, Georgia, Illinois. 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