ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study of RAD001 in Patients With Relapsed/Refractory Hodgkin Lymphoma That Has Progressed After High-dose Chemotherapy and Autologous Stem Cell Transplant and/or After Gemcitabine- or Vinorelbine- or Vinblastine-based Treatment.

ClinicalTrials.gov ID: NCT01022996

Public ClinicalTrials.gov record NCT01022996. 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 May 5, 2026, 12:16 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

An Open-label, Single-arm Phase II Study of RAD001 in Patients With Relapsed/Refractory Classical Hodgkin Lymphoma

Study identification

NCT ID
NCT01022996
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
57 participants

Conditions and interventions

Interventions

  • Everolimus (RAD001) 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
Nov 30, 2009
Primary completion
Oct 31, 2014
Completion
Oct 31, 2014
Last update posted
May 17, 2016

2009 – 2014

United States locations

U.S. sites
16
U.S. states
15
U.S. cities
16
Facility City State ZIP Site status
University of California at Los Angeles UCLS School of Medicine Los Angeles California 90095
Rocky Mountain Cancer Centers RMCC - Aurora Greenwood Village Colorado
MD Anderson Cancer Center - Orlando Orlando Florida 32806
Emory University School of Medicine/Winship Cancer Institute Emory University Med School Atlanta Georgia 30322
Lurie Children's Hospital of Chicago Robert H. Lurie Comp Cancer Chicago Illinois 60611
Indiana University Simon Cancer Center Indianapolis Indiana 46202
Dana Farber Cancer Institute Boston Massachusetts 02115
Karmanos Cancer Institute Karmanos-1 Detroit Michigan 48201
Mayo Clinic - Rochester Mayo Lymphoma Group Rochester Minnesota 55905
Washington University School Of Medicine-Siteman Cancer Ctr StudyCoordinator:CLBH589B2201 St Louis Missouri 63110
New York Presbyterian Hospital Weill Cornell Med Ctr New York New York 10021
Duke University Medical Center Duke University Medical Ctr Durham North Carolina 27710
University of Tennessee Cancer Institute Univ Tennessee Cancer Memphis Tennessee 38104
University of Texas/MD Anderson Cancer Center Dept.ofMDAndersonCancerCtr(3) Houston Texas 77030-4009
University of Wisconsin Comprehensive Cancer Center Clinical Science Center - H4 Madison Wisconsin 53792
Medical College of Wisconsin 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01022996, 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 May 17, 2016 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01022996 live on ClinicalTrials.gov.

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