Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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: Completed Phase 3 study, sponsored by Seagen.

NCT01100502 is a Phase 3 study that has completed, run by Seagen. The registered enrollment target is 329 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

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).

Primary Outcome

Time from date of randomization to the first documentation of disease progression by independent review or to death due to any cause, whichever comes first

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
Seagen

84 total trials

What the finished NCT01100502 record still lists

NCT01100502 is an interventional study that assigns participants to a tested intervention. The registered 329 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (57% lower).

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

NCT01100502 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT01100502's enrollment target sits among peer trials

329 1074th of 2000 higher than 927 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT06036446 · 329 participants · NA

    LATe Cerclage in High-risk Pregnancies (LATCH)

  • NCT00359684 · 330 participants

    Use of Cysteamine in the Treatment of Cystinosis

  • NCT03817502 · 330 participants · Phase 3

    Efficacy and Safety of Cariprazine in the Treatment of Adolescent Participants (13 to 17 Years of Age) With Schizophrenia

  • NCT03922724 · 330 participants · Phase 2

    Allogeneic Hematopoietic Cell Transplantation for Peripheral T Cell Lymphoma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01100502, the US trial registry maintained by the National Library of Medicine. NCT01100502 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.