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Completed Phase 3 Interventional Results available

Alisertib (MLN8237) or Investigator's Choice in Patients With Relapsed/Refractory Peripheral T-Cell Lymphoma

ClinicalTrials.gov ID: NCT01482962

Public ClinicalTrials.gov record NCT01482962. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 7:58 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Randomized, Two-Arm, Open-Label, Multicenter, International Trial of Alisertib (MLN8237) or Investigator's Choice (Selected Single Agent) in Patients With Relapsed or Refractory Peripheral T-Cell Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a phase 3, randomized, 2-arm, open-label, international trial evaluating alisertib compared with single-agent treatment, as selected by the investigator from the offered options of pralatrexate or gemcitabine or romidepsin, in participants with relapsed or refractory peripheral T-cell lymphoma (PTCL). Note: romidepsin was not used as a single-agent comparator outside the United States of America (USA) as supply was not available.

Study identification

NCT ID
NCT01482962
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
271 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 11, 2012 (Actual)
Primary completion
Jun 30, 2015 (Actual)
Completion
Dec 18, 2017 (Actual)
Last update posted
Jul 31, 2018

2012 – 2017

United States locations

U.S. sites
24
U.S. states
19
U.S. cities
24
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed La Jolla California — —
Not listed Orlando Florida — —
Not listed Tampa Florida — —
Not listed Indianapolis Indiana — —
Not listed Iowa City Iowa — —
Not listed Boston Massachusetts — —
Not listed Detroit Michigan — —
Not listed Rochester Minnesota — —
Not listed Jefferson City Missouri — —
Not listed St Louis Missouri — —
Not listed Lebanon New Hampshire — —
Not listed Hackensack New Jersey — —
Not listed Buffalo New York — —
Not listed New York New York — —
Not listed Syracuse New York — —
Not listed Durham North Carolina — —
Not listed Columbus Ohio — —
Not listed Toledo Ohio — —
Not listed Charleston South Carolina — —
Not listed Houston Texas — —
Not listed Burlington Vermont — —
Not listed Seattle Washington — —
Not listed Morgantown West Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 127 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01482962, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 31, 2018 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01482962 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →