Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 1 Interventional

Temsirolimus, Dexamethasone, Mitoxantrone Hydrochloride, Vincristine Sulfate, and Pegaspargase in Treating Young Patients With Relapsed Acute Lymphoblastic Leukemia or Non-Hodgkin Lymphoma

ClinicalTrials.gov ID: NCT01403415

Public ClinicalTrials.gov record NCT01403415. 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 21, 2026, 9:34 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 1 Study of Temsirolimus in Combination With Intensive Re-induction Therapy for Children With Relapsed Acute Lymphoblastic Leukemia and Non-Hodgkin Lymphoma

Brief summary

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

This phase I trial studies the side effects and the best dose of temsirolimus when given together with dexamethasone, mitoxantrone hydrochloride, vincristine sulfate, and pegaspargase in treating young patients with relapsed acute lymphoblastic leukemia or non-Hodgkin lymphoma. Temsirolimus may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as dexamethasone, mitoxantrone hydrochloride, vincristine sulfate, and pegaspargase work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving temsirolimus with combination chemotherapy may be and effective treatment for acute lymphoblastic leukemia or non-Hodgkin lymphoma.

Study identification

NCT ID
NCT01403415
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
13 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Year to 21 Years
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
Sep 2011 (Type not available)
Primary completion
May 2015 (Actual)
Completion
Not listed
Last update posted
Jul 10, 2015

Started 2011

United States locations

U.S. sites
30
U.S. states
21
U.S. cities
29
Facility City State ZIP Site status
Children's Hospital of Alabama Birmingham Alabama 35233 —
Phoenix Childrens Hospital Phoenix Arizona 85016 —
Childrens Hospital of Orange County Orange California 92868 —
Lucile Packard Children's Hospital Stanford University Palo Alto California 94304 —
Rady Children's Hospital - San Diego San Diego California 92123 —
UCSF Medical Center-Parnassus San Francisco California 94143 —
Children's National Medical Center Washington D.C. District of Columbia 20010 —
Children's Healthcare of Atlanta - Egleston Atlanta Georgia 30322 —
Lurie Children's Hospital-Chicago Chicago Illinois 60611 —
Riley Hospital for Children Indianapolis Indiana 46202 —
C S Mott Children's Hospital Ann Arbor Michigan 48109 —
Children's Hospitals and Clinics of Minnesota - Minneapolis Minneapolis Minnesota 55404 —
University of Minnesota Medical Center-Fairview Minneapolis Minnesota 55455 —
University of Mississippi Medical Center Jackson Mississippi 39216 —
The Childrens Mercy Hospital Kansas City Missouri 64108 —
Washington University School of Medicine St Louis Missouri 63110 —
Columbia University Medical Center New York New York 10032 —
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 —
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229 —
Rainbow Babies and Childrens Hospital Cleveland Ohio 44106 —
Nationwide Children's Hospital Columbus Ohio 43205 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Oregon Health and Science University Portland Oregon 97239 —
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 —
Children's Hospital of Pittsburgh of UPMC Pittsburgh Pennsylvania 15224 —
Vanderbilt University/Ingram Cancer Center Nashville Tennessee 37232 —
UT Southwestern/Simmons Cancer Center-Dallas Dallas Texas 75390 —
Baylor College of Medicine Houston Texas 77030 —
Primary Children's Hospital Salt Lake City Utah 84113 —
Midwest Children's Cancer Center Milwaukee Wisconsin 53226 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01403415, 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 10, 2015 · Synced Oct 21, 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 public registry record, listed eligibility criteria, and available contact information for NCT01403415 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →