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NCT02169505 · ClinicalTrials.gov registry record · Phase 2

Brentuximab Vedotin in High-Risk CD30+ Lymphoma Post Allogeneic Stem Cell Transplantation (AlloSCT)

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Terminated
Registry status
Phase 2
Development phase
2
Enrollment target

NCT02169505: Clinical Trial Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT02169505 is a Phase 2 study that was terminated before completion, run by M.D. Anderson Cancer Center. The registered enrollment target is 2 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02169505, a Phase 2 study, was terminated before completion, sponsored by M.D. Anderson Cancer Center.

TERMINATED
Registry status
Phase 2
Development phase
2 participants
Enrollment target

Study Summary

The goal of this clinical research study is to study the safety of ADCETRISTM (brentuximab vedotin) in patients with Hodgkin lymphoma or ALCL who have had an allogeneic or haploidentical stem cell transplant. Another goal of this study is to learn if brentuximab vedotin can help to prevent the disease from coming back.

Primary Outcome

Safety is defined by no more than two secondary graft failures within 6 months of transplant (Day 0), based on an observed graft failure rate of \<10% using standard of care treatment. If at any time more than two of these events are observed during the specified time frame, the study will be stopped and no further patients will be accrued.

Interventions

  • DRUG Brentuximab Vedotin

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2015-05-22
Est. Completion 2017-08-14
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

Why NCT02169505 stopped before completion

NCT02169505 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Brentuximab Vedotin is the first listed.

NCT02169505 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02169505 about?

NCT02169505 is a clinical study titled "Brentuximab Vedotin in High-Risk CD30+ Lymphoma Post Allogeneic Stem Cell Transplantation (AlloSCT)". The goal of this clinical research study is to study the safety of ADCETRISTM (brentuximab vedotin) in patients with Hodgkin lymphoma or ALCL who have had an allogeneic or haploidentical stem cell transplant. Another goal of this study is to learn if brentuximab vedotin can help to prevent the disea...

What is the current status of trial NCT02169505?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 2 participants. The study started on 2015-05-22. Estimated completion is 2017-08-14.

What interventions are being tested in trial NCT02169505?

The interventions under investigation include: Brentuximab Vedotin (DRUG).

Who is sponsoring clinical trial NCT02169505?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02169505's enrollment target sits among peer trials

2 2001st of 2000 the lowest of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02169505, the US trial registry maintained by the National Library of Medicine. NCT02169505 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.