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NCT02227199 · ClinicalTrials.gov registry record · Phase 1

Brentuximab Vedotin, Ifosfamide, Carboplatin, and Etoposide in Treating Patients With Relapsed or Refractory Hodgkin Lymphoma

A Phase 1 study, sponsored by University of Washington.

Completed
Registry status
Phase 1
Development phase
45
Enrollment target

NCT02227199 is a Phase 1 study that has completed, run by University of Washington. The registered enrollment target is 45 participants.

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The verdict

NCT02227199, a Phase 1 study, has completed, sponsored by University of Washington.

COMPLETED
Registry status
Phase 1
Development phase
45 participants
Enrollment target

Study Summary

This phase I/II trial studies the side effects and best dose of brentuximab vedotin that can be combined with ifosfamide, carboplatin, and etoposide in treating patients with Hodgkin lymphoma that has come back (relapsed) or is not responding to treatment (refractory). Monoclonal antibody-drug conjugates, such as brentuximab vedotin, can block cancer growth in different ways by targeting certain cells. Chemotherapy drugs, such as ifosfamide, carboplatin, and etoposide, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving brentuximab vedotin together with an ifosfamide, carboplatin, and etoposide chemotherapy regimen may kill more cancer cells.

Interventions

  • DRUG Carboplatin
  • OTHER Laboratory Biomarker Analysis
  • DRUG Etoposide
  • DRUG Brentuximab Vedotin
  • DRUG Ifosfamide

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2014-10-10
Est. Completion 2025-07-28
Phase Phase 1

Sponsor

University of Washington

1,048 total trials

What the Registry Record Tells You About NCT02227199

The ClinicalTrials.gov registry entry for NCT02227199 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Carboplatin is the first listed.

NCT02227199 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02227199 about?

NCT02227199 is a clinical study titled "Brentuximab Vedotin, Ifosfamide, Carboplatin, and Etoposide in Treating Patients With Relapsed or Refractory Hodgkin Lymphoma". This phase I/II trial studies the side effects and best dose of brentuximab vedotin that can be combined with ifosfamide, carboplatin, and etoposide in treating patients with Hodgkin lymphoma that has come back (relapsed) or is not responding to treatment (refractory). Monoclonal antibody-drug conju...

What is the current status of trial NCT02227199?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 45 participants. The study started on 2014-10-10. Estimated completion is 2025-07-28.

What interventions are being tested in trial NCT02227199?

The interventions under investigation include: Carboplatin (DRUG), Laboratory Biomarker Analysis (OTHER), Etoposide (DRUG), Brentuximab Vedotin (DRUG), Ifosfamide (DRUG).

Who is sponsoring clinical trial NCT02227199?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.