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Spots Global Cancer Trial Database for Safety and Efficacy Study of Abraxane in Combination With Carboplatin to Treat Advanced NSCL Cancer in the Elderly

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Trial Identification

Brief Title: Safety and Efficacy Study of Abraxane in Combination With Carboplatin to Treat Advanced NSCL Cancer in the Elderly

Official Title: Safety and Efficacy of Nab-paclitaxel (Abraxane) in Combination With Carboplatin as First Line Treatment in Elderly Subjects With Advance Non-Small Cell Lung Cancer (NSCLC): A Phase IV, Randomized, Open-Label, Multicenter Study (Abound.70+)

Study ID: NCT02151149

Study Description

Brief Summary: Study comparing two regimens of nab-paclitaxel and carboplatin combination in elderly subjects (≥ 70 years old) with advanced NSCLC

Detailed Description: This is a Phase IV, randomized, open-label, multicenter study of continuous weekly versus weekly times three with one-week break nab-paclitaxel in combination with carboplatin as first-line treatment in elderly subjects (≥ 70 years old) with advanced non small cell lung cancer who have not received prior chemotherapy for their advanced disease and are not candidates for curative surgery or radiation therapy. The primary study endpoint is the percentage of subjects with either peripheral neuropathy or myelosuppression adverse events. Patients will continue treatment until they develop progressive disease, unacceptable side-effects or wish to withdraw from the study, according to local standard of care. Patients will have radiographic evaluations every 6 weeks while on treatment.

Eligibility

Minimum Age: 70 Years

Eligible Ages: OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arizona Clinical Research Center, Tucson, Arizona, United States

Genesis Cancer Center, Hot Springs, Arkansas, United States

Comprehensive Blood and Cancer Center, Bakersfield, California, United States

Saint Jude Heritage Medical Center, Fullerton, California, United States

Global Cancer Research Institute (GCRI), Inc., Gilroy, California, United States

Ventura County Hematology-Oncology Specialists, Oxnard, California, United States

Central Coast Medical Oncology Corporation, Santa Maria, California, United States

University of California Los Angeles, Santa Monica, California, United States

Rocky Mountain Cancer Centers, LLP, Denver, Colorado, United States

St Mary's Hospital and Regional Medical Center, Grand Junction, Colorado, United States

Lynn Cancer Institute, Boca Raton, Florida, United States

Baptist Cancer Inst, Jacksonville, Florida, United States

Ocala Oncology Center, Ocala, Florida, United States

Florida Hospital Cancer Institute, Orlando, Florida, United States

Northshore University Healthsystem Research Institute, Evanston, Illinois, United States

Oncology Specialists, S.C., Niles, Illinois, United States

Franciscan St. Francis Health, Indianapolis, Indiana, United States

Cancer Center of Kansas, Wichita, Kansas, United States

Western Kentucky Hematology and Oncology Group, Paducah, Kentucky, United States

West Jeffersion Medical Center, Marrero, Louisiana, United States

Ochsner Medical Institutions, New Orleans, Louisiana, United States

Medstar Health Research Institute, Baltimore, Maryland, United States

Reliant Medical Group, Worcester, Massachusetts, United States

Henry Ford Health System, Detroit, Michigan, United States

Nebraska Methodist Hospital, Omaha, Nebraska, United States

Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, United States

Center for Cancer and Hematologic Disease, Cherry Hill, New Jersey, United States

Regional Cancer Care Associates LLC, East Brunswick, New Jersey, United States

Saint Barnabas Medical Center, Livingston, New Jersey, United States

Carol G Simon Cancer Center, Morristown, New Jersey, United States

Somerset Hematology-Oncology Associates, Somerville, New Jersey, United States

Regional Cancer Care Associates LLC- Sparta division, Sparta, New Jersey, United States

Montefiore Medical Center, Bronx, New York, United States

Brookdale University Hospital and Medical Center, Brooklyn, New York, United States

Broome Oncology, LLC, Johnson City, New York, United States

Clinical Research Alliance, Lake Success, New York, United States

SUNY Upstate Medical University Medicine Oncology, Syracuse, New York, United States

Lineberger Cancer Center, Chapel Hill, North Carolina, United States

Levine Cancer Institute, Charlotte, North Carolina, United States

Forsyth Memorial Hospital, Inc., Winston-Salem, North Carolina, United States

St Elizabeth Hospital, Youngstown, Ohio, United States

Cancer Centres of Southwest Okahoma Research, Lawton, Oklahoma, United States

Good Samaritan Hospital Corvalis, Corvallis, Oregon, United States

Oregon Health and Science University, Portland, Oregon, United States

Penn State Milton S Hershey Medical Center, Hershey, Pennsylvania, United States

Perelman Center for Advanced Medicine, Philadelphia, Pennsylvania, United States

Thomas Jefferson University Medical College, Philadelphia, Pennsylvania, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

Allegheny General Hospital, Pittsburgh, Pennsylvania, United States

Texas Oncology, P.A.-Amarillo, Amarillo, Texas, United States

Baylor University Medical Center at Dallas, Dallas, Texas, United States

UTMB Galveston, Galveston, Texas, United States

Texas Oncology, PA - Longview, Longview, Texas, United States

Virginia Mason Cancer Center, Seattle, Washington, United States

Northwest Cancer Specialists, P.C., Vancouver, Washington, United States

Contact Details

Name: Teng Jin Ong

Affiliation: Celgene

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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