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Spots Global Cancer Trial Database for Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy in Non-small Cell Lung Cancer (NSCLC)

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Trial Identification

Brief Title: Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy in Non-small Cell Lung Cancer (NSCLC)

Official Title: A Randomized Phase II Study of Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy for Advance Non-small Cell Lung Cancer(NSCLC)

Study ID: NCT01137968

Study Description

Brief Summary: The purpose of this is to evaluate the efficacy and safety of imetelstat (GRN163L) as maintenance therapy for patients with advanced stage NSCLC who have not progressed after 4 cycles of platinum based therapy. Participants will be randomized in a 2:1 ratio to imetelstat + standard of care versus standard of care alone. Participants who received bevacizumab with their induction chemotherapy will continue to receive bevacizumab on this study.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Achieve Clinical Research, Llc, Birmingham, Alabama, United States

Clearview Cancer Institute, Huntsville, Alabama, United States

Pacific Cancer Medical Center, Inc., Anaheim, California, United States

Cancer Care Associates of Fresno Medical Group Inc, Fresno, California, United States

St. Joseph's Hospital, Orange, California, United States

Kaiser Permanente Medical Center, Vallejo, California, United States

University of Colorado Denver School of Medicine, Aurora, Colorado, United States

Florida Cancer Specialists, Fort Myers, Florida, United States

Integrated Community Oncology Network, Jacksonville, Florida, United States

H. Moffitt Lee Cancer Center, Tampa, Florida, United States

Ingalls Memorial Hospital, Harvey, Illinois, United States

Cancer Center of Kansas, Wichita, Kansas, United States

Montgomery Cancer Center, Mt. Sterling, Kentucky, United States

Auerbach Hematology Oncology, Baltimore, Maryland, United States

Karmanos Cancer Institute, Detroit, Michigan, United States

Hematology Oncology Centers, Billings, Montana, United States

Blumenthal Cancer Center, Charlotte, North Carolina, United States

Kaiser Northwest, Portland, Oregon, United States

South Carolina Oncology Associates, Columbia, South Carolina, United States

The Jones Clinic, Germantown, Tennessee, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

UT Southwestern Medical Center, Dallas, Texas, United States

Scott and White Memorial Hospital (Texas A & M), Temple, Texas, United States

Swedish Cancer Institute, Seattle, Washington, United States

Northwest Medical Specialties, Tacoma, Washington, United States

University of Wisconsin, Madison, Wisconsin, United States

Hôpital Charles Lemoyne, Greenfield Park, Quebec, Canada

Hospital Notre-Dame, Montreal, Quebec, Canada

Krankenhaus Grosshansdorf, Grosshansdorf, Hamburg, Germany

Asklepios Klinik Gauting GmbH, Gauting, Munich, Germany

Klinikum rechts der Isar der TU München, Munchen, Munich, Germany

Krankenhaus Nordwest, Frankfurt, , Germany

Universitaetsklinikum Mainz, Mainz, , Germany

Contact Details

Name: Joan Schiller, MD

Affiliation: University of Texas

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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