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COMPLETED Phase 1

Study of Cabiralizumab in Patients With Pigmented Villonodular Synovitis / Diffuse Type Tenosynovial Giant Cell Tumor

NCT02471716 · View on ClinicalTrials.gov ↗

Study Summary

This is a phase 1/2 single arm, open-label, safety, tolerability, and PK study of cabiralizumab in PVNS/dt-TGCT patients.

Interventions

  • BIOLOGICAL FPA008

Study Locations (12)

Other

  • Institut Bergonie- CRLCC de Bordeaux et du Sud-Ouest — Bordeaux
  • Centre Léon Bérard — Lyon
  • Leiden University Medical Center — Leiden
  • Klinika Nowotworow Tkanek Miekkich, Kosci i Czerniakow, Centrum Onkologii-Instytut im. M. Sklodowskiej-Curie — Warsaw
  • University Hospitals Birmingham NHS Foundation Trust — Birmingham
  • Oxford University Hospital NHS Trust — Oxford

California

  • Cedars-Sinai Medical Center — Los Angeles
  • Sarcoma Oncology Research Center LLC — Santa Monica
  • Stanford Medicine — Stanford

Massachusetts

  • Dana-Farber Cancer Institute — Boston

Texas

  • The University of Texas, MD Anderson Cancer Center — Houston

Jongno-gu

  • Seoul National University Hospital — Seoul

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2015-06
Est. Completion 2020-04-30
Phase Phase 1

Sponsor

Five Prime Therapeutics

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02471716

The ClinicalTrials.gov registry entry for NCT02471716 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 66 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Five Prime Therapeutics, which has 4 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 Tenosynovial Giant Cell Tumor appearing as the primary indexed condition, and to 1 intervention — of which FPA008 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: NCT02471716 reports 12 study locations spanning 5 distinct geographic areas — top geographies include Other, California, Massachusetts. 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 NCT02471716 about?

NCT02471716 is a clinical study titled "Study of Cabiralizumab in Patients With Pigmented Villonodular Synovitis / Diffuse Type Tenosynovial Giant Cell Tumor". This is a phase 1/2 single arm, open-label, safety, tolerability, and PK study of cabiralizumab in PVNS/dt-TGCT patients.

What is the current status of trial NCT02471716?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 66 participants. The study started on 2015-06. Estimated completion is 2020-04-30.

What conditions does trial NCT02471716 study?

This clinical trial studies the following conditions: Tenosynovial Giant Cell Tumor, Pigmented Villonodular Synovitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02471716?

The interventions under investigation include: FPA008 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02471716?

This trial is sponsored by Five Prime Therapeutics, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02471716 being conducted?

This trial has 12 study locations across California, Massachusetts, Texas, Jongno-gu. 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