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NCT01100502 · ClinicalTrials.gov registry record · Phase 3

A Phase 3 Study of Brentuximab Vedotin (SGN-35) in Patients at High Risk of Residual Hodgkin Lymphoma Following Stem Cell Transplant (The AETHERA Trial)

A Phase 3 study, sponsored by Seagen.

Completed
Registry status
Phase 3
Development phase
329
Enrollment target

NCT01100502 is a Phase 3 study that has completed, run by Seagen. The registered enrollment target is 329 participants.

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The verdict

NCT01100502, a Phase 3 study, has completed, sponsored by Seagen.

COMPLETED
Registry status
Phase 3
Development phase
329 participants
Enrollment target

Study Summary

This is a randomized, double-blind, placebo-controlled, multicenter phase 3 trial to evaluate the efficacy and safety of brentuximab vedotin (SGN-35) and best supportive care (BSC) compared to placebo and BSC in treatment of residual Hodgkin lymphoma (HL) following autologous stem cell transplant (ASCT).

Interventions

  • DRUG placebo
  • DRUG brentuximab vedotin

Trial Details

FieldValue
Enrollment Target 329 participants
Start Date 2010-04-30
Est. Completion 2020-04-27
Phase Phase 3

Sponsor

Seagen

84 total trials

What the Registry Record Tells You About NCT01100502

The ClinicalTrials.gov registry entry for NCT01100502 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 329 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Seagen, which has 84 total studies on file at ClinicalTrials.gov.

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

NCT01100502 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01100502 about?

NCT01100502 is a clinical study titled "A Phase 3 Study of Brentuximab Vedotin (SGN-35) in Patients at High Risk of Residual Hodgkin Lymphoma Following Stem Cell Transplant (The AETHERA Trial)". This is a randomized, double-blind, placebo-controlled, multicenter phase 3 trial to evaluate the efficacy and safety of brentuximab vedotin (SGN-35) and best supportive care (BSC) compared to placebo and BSC in treatment of residual Hodgkin lymphoma (HL) following autologous stem cell transplant (A...

What is the current status of trial NCT01100502?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 329 participants. The study started on 2010-04-30. Estimated completion is 2020-04-27.

What interventions are being tested in trial NCT01100502?

The interventions under investigation include: placebo (DRUG), brentuximab vedotin (DRUG).

Who is sponsoring clinical trial NCT01100502?

This trial is sponsored by Seagen, which has 84 total clinical trials registered on ClinicalTrials.gov.

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

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.