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Spots Global Cancer Trial Database for Safety of Adding IMO-2055 to Erlotinib + Bevacizumab in 2nd Line Treatment for Patients With NSCLC

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Safety of Adding IMO-2055 to Erlotinib + Bevacizumab in 2nd Line Treatment for Patients With NSCLC

Official Title: Open-Label Phase 1b Study of Erlotinib Plus Bevacizumab and IMO-2055 in Patients With Non-Small Cell Lung Cancer Who Have Progressed Following Initial Chemotherapy for Advanced or Metastatic Disease

Study ID: NCT00633529

Interventions

IMO-2055

Study Description

Brief Summary: To evaluate the safety of the proposed Phase II dosage of the investigational drug IMO 2055 when combined with erlotinib and bevacizumab in patients with previously treated advanced NSCLC.

Detailed Description: Phase 1b study of escalating doses of weekly subcutaneous IMO-2055 combined with fixed standard dose regimens of oral erlotinib (daily) and IV bevacizumab (every 3 weeks) in patients with previously treated advanced NSCLC.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Cancer Centers of Florida, Ocoee, Florida, United States

Central Indiana Cancer Centers, Indianapolis, Indiana, United States

New York Oncology Hematology P.C., Albany, New York, United States

Mary Crowley Medical Research Center, Dallas, Texas, United States

Cancer Therapy and Research Center, San Antonio, Texas, United States

Tyler Cancer Center, Tyler, Texas, United States

Virginia Oncology Associates, Norfolk, Virginia, United States

Northwest Cancer Specialists, Vancouver, Washington, United States

Yakima Valley Memorial Hospital/North Shore Cancer Lodge, Yakima, Washington, United States

Contact Details

Name: Phil Breitfeld, MD

Affiliation: EMD Serono

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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