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NCT02822586 · ClinicalTrials.gov registry record · Phase 1

TSEB and Brentuximab for Treatment of Mycosis Fungoides & Sezary Syndrome

A Phase 1 study, sponsored by Virginia Commonwealth University.

Completed
Registry status
Phase 1
Development phase
5
Enrollment target

NCT02822586: Completed Phase 1 study, sponsored by Virginia Commonwealth University.

NCT02822586 is a Phase 1 study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 5 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02822586, a Phase 1 study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
Phase 1
Development phase
5 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the cutaneous toxicity and treatment response associated with administering concurrent TSEB and brentuximab vedotin in patients with mycosis fungoides or Sézary Syndrome.

Primary Outcome

Selected cutaneous adverse events (AEs) that occurred during treatment or during the 3 months following initiation of study treatment and that are characterized and graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.0 (NCI CTCAE v4.0) including ≥ grade 3 AEs and selected grade 2 AEs

Interventions

  • DRUG Brentuximab vedotin
  • RADIATION TSEB Therapy

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2016-12-19
Est. Completion 2019-04-29
Phase Phase 1
Virginia Commonwealth University

558 total trials

What the finished NCT02822586 record still lists

NCT02822586 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which Brentuximab vedotin is the first listed.

NCT02822586 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02822586 about?

NCT02822586 is a clinical study titled "TSEB and Brentuximab for Treatment of Mycosis Fungoides & Sezary Syndrome". The purpose of this study is to evaluate the cutaneous toxicity and treatment response associated with administering concurrent TSEB and brentuximab vedotin in patients with mycosis fungoides or Sézary Syndrome.

What is the current status of trial NCT02822586?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 5 participants. The study started on 2016-12-19. Estimated completion is 2019-04-29.

What interventions are being tested in trial NCT02822586?

The interventions under investigation include: Brentuximab vedotin (DRUG), TSEB Therapy (RADIATION).

Who is sponsoring clinical trial NCT02822586?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02822586's enrollment target sits among peer trials

5 1989th of 2000 higher than 6 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02822586, the US trial registry maintained by the National Library of Medicine. NCT02822586 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.