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Spots Global Cancer Trial Database for Study Assessing Safety, Pharmacokinetics and Efficacy of CC-223 With Either Erlotinib or Oral Azacitidine in Advanced Non-Small Cell Lung Cancer

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Trial Identification

Brief Title: Study Assessing Safety, Pharmacokinetics and Efficacy of CC-223 With Either Erlotinib or Oral Azacitidine in Advanced Non-Small Cell Lung Cancer

Official Title: A PHASE 1B, MULTI-CENTER, OPEN-LABEL STUDY OF THE MTOR KINASE INHIBITOR CC-223 IN COMBINATION WITH ERLOTINIB OR ORAL AZACITIDINE IN ADVANCED NON-SMALL CELL LUNG CANCER

Study ID: NCT01545947

Study Description

Brief Summary: The main purpose of this first study combining an investigational dual mTOR inhibitor, CC-223, with other agents (erlotinib or the investigational agent, oral azacitidine) is to establish a maximum tolerated dose level for each combination in order to evaluate their effects in future clinical trials for advanced non-small cell lung cancer.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Cedars Sinai Medical Center, Inflammatory Bowel Disease Center, Los Angeles, California, United States

University of California, San Francisco, San Francisco, California, United States

NYU School of Medicine, New York, New York, United States

Cancer Center of the Carolinas, Greenville, South Carolina, United States

Henry-Joyce Cancer Clinic, Nashville, Tennessee, United States

Mary Crowley Cancer Research Centers - Medical City, Dallas, Texas, United States

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Vall d´Hebron University Hospital, Barcelona, , Spain

Hospital Virgen del Rocio Servicio de Hematologia, Sevilla, , Spain

Contact Details

Name: Kristen Hege, MD

Affiliation: Celgene Corporation

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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