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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 Jul 23, 2026, 6:05 PM 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

Study identification

NCT ID
NCT01482962
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Millennium Pharmaceuticals, Inc.
Industry
Enrollment
271 participants

Conditions and interventions

Interventions

  • Alisertib Drug
  • Pralatrexate Drug
  • Gemcitabine Drug
  • Romidepsin Drug

Drug

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 10, 2012
Primary completion
Jun 29, 2015
Completion
Dec 17, 2017
Last update posted
Jul 30, 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 30, 2018 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01482962 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →