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Spots Global Cancer Trial Database for CPG 7909 Injection in Non-Small Cell Lung Cancer

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Trial Identification

Brief Title: CPG 7909 Injection in Non-Small Cell Lung Cancer

Official Title: Promune™ (CPG 7909 Injection) In Combination With Chemotherapy In Patients With Advanced Or Metastatic Non-Small Cell Lung Cancer, A Randomized, Multi-Center, Controlled, Phase 2 Study

Study ID: NCT00070629

Study Description

Brief Summary: Eligible patients will be randomized in a ratio of 2:1 to receive either chemotherapy (a taxane and a platinum compound) plus CPG 7909 Injection or chemotherapy alone. Protocol therapy will be administered until disease progression or intolerable toxicity. CpG 7909 Injection will be administered subcutaneously, on Weeks 2 and 3 of each three-week cycle (days 8 and 15) and chemotherapy will be administered on Week 1 (Day 1). Patients will undergo complete disease evaluation at the end of every other treatment cycle until disease progression.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Office of Ronald Yanagihara, Gilroy, California, United States

Kenmar Research Institute, LLC, Los Angeles, California, United States

Comprehensive Cancer Center of the Dessert, Palm Springs, California, United States

Florida Cancer Specialist, Fort Myers, Florida, United States

Indiana Hematology and Oncology Associates, Indianapolis, Indiana, United States

Medical Center Vincennes, Vincennes, Indiana, United States

Kentucky Cancer Clinic, Hazard, Kentucky, United States

University of Minnesota, Minneapolis, Minnesota, United States

Southeast Nebraska Hematology Oncology Consultants, PC, Lincoln, Nebraska, United States

VA New Jersey Health Care System, East Orange, New Jersey, United States

HemOnCare, Brooklyn, New York, United States

Cancer Care of Western North Carolina, Asheville, North Carolina, United States

Providence Portland Medical Center, Portland, Oregon, United States

Cancer Care Institute of Carolina, Aiken, South Carolina, United States

Charleston Hematology/Oncology, PA, Charleston, South Carolina, United States

The Family Cancer Center, Collierville, Tennessee, United States

Marshfield Clinic, Marshfield, Wisconsin, United States

Queen Elizabeth II Health, Halifax, Nova Scotia, Canada

Ottawa Regional Cancer Center, Ottawa, Ontario, Canada

McGill University, Montreal, Quebec, Canada

Staedtisches Krankenhaus Martha-Maria, Halle-Dolau, , Germany

Universitätsklinikum Mannheim der Universität Heidelberg, Heidelberg, , Germany

St. Vincentius-Kliniken gAG, Hamatologie-Onkologie, Karlsruhe, , Germany

Klinikum Rechts der Isar, Munchen, , Germany

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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