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Spots Global Cancer Trial Database for A Study of IMC-A12 or Ramucirumab Plus Mitoxantrone and Prednisone in Prostate Cancer

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Trial Identification

Brief Title: A Study of IMC-A12 or Ramucirumab Plus Mitoxantrone and Prednisone in Prostate Cancer

Official Title: A Phase 2, Multicenter, Randomized Study of IMC-A12 or IMC-1121B Plus Mitoxantrone and Prednisone in Metastatic Androgen-Independent Prostate Cancer (AIPC) Following Disease Progression on Docetaxel-Based Chemotherapy

Study ID: NCT00683475

Conditions

Prostate Cancer

Study Description

Brief Summary: The purpose of this study is to determine whether IMC-A12 or IMC-1121B (ramucirumab) with Mitoxantrone and Prednisone is effective in the treatment of metastatic androgen- independent prostate cancer (APIC).

Detailed Description: Prostate cancer is the most frequently diagnosed cancer in men and the second leading cause of cancer-related death in men in the United States. Chemotherapy, either as a single agent or in combination, may lead to clinical response, pain control, and/or improved quality of life. Docetaxel is now the first-line standard therapy for AIPC. Mitoxantrone was approved in 1996 for use in combination with corticosteroids as initial chemotherapy for pain related to advanced Hormone Refractory Prostate Cancer (HRPC). Hormonal manipulations and docetaxel-based chemotherapy are often effective in metastatic prostate cancer; however, disease becomes refractory to these interventions in the majority of men. Although mitoxantrone continues to be a significant agent in the treatment of HRPC, there exists a need for more efficacious therapy in docetaxel-refractory- AIPC. Because of the potential contribution of Insulin Like Growth Factor Receptor (IGF-IR) and VEGFR-2 mediated pathways in prostate cancer pathogenesis, it is hypothesized that each of these biological agents in combination with mitoxantrone and prednisone will result in clinically meaningful activity in AIPC. Therefore, ImClone plans to conduct a randomized Phase 2 trial to assess the safety and efficacy of IMC-A12 or IMC-1121B (ramucirumab) in combination with mitoxantrone and prednisone in participants with AIPC.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

ImClone Investigational Site, La Jolla, California, United States

ImClone Investigational Site, New Haven, Connecticut, United States

ImClone Investigational Site, Boca Raton, Florida, United States

ImClone Investigational Site, Port St. Lucie, Florida, United States

ImClone Investigational Site, Atlanta, Georgia, United States

ImClone Investigational Site, Chicago, Illinois, United States

ImClone Investigational Site, Chlcago, Illinois, United States

ImClone Investigational Site, Evanston, Illinois, United States

ImClone Investigational Site, Maryville, Illinois, United States

ImClone Investigational Site, Cedar Rapids, Iowa, United States

ImClone Investigational Site, Metairie, Louisiana, United States

ImClone Investigational Site, Ann Arbor, Michigan, United States

ImClone Investigational Site, Rochester, Minnesota, United States

ImClone Investigational Site, St Louis, Missouri, United States

ImClone Investigational Site, Billings, Montana, United States

ImClone Investigational Site, Roseland, New Jersey, United States

ImClone Investigational Site, Buffalo, New York, United States

ImClone Investigational Site, East Setauket, New York, United States

ImClone Investigational Site, New York, New York, United States

ImClone Investigational Site, New York, New York, United States

ImClone Investigational Site, New York, New York, United States

ImClone Investigational Site, New York, New York, United States

ImClone Investigational Site, Durham, North Carolina, United States

ImClone Investigational Site, Cleveland, Ohio, United States

ImClone Investigational Site, Philadelphia, Pennsylvania, United States

ImClone Investigational Site, Pittsburgh, Pennsylvania, United States

ImClone Investigational Site, Greenville, South Carolina, United States

ImClone Investigational Site, Knoxville, Tennessee, United States

ImClone Investigational Site, Nashville, Tennessee, United States

ImClone Investigational Site, Abilene, Texas, United States

ImClone Investigational Site, Dallas, Texas, United States

ImClone Investigational Site, Houston, Texas, United States

ImClone Investigational Site, Houston, Texas, United States

ImClone Investigational Site, Seattle, Washington, United States

ImClone Investigational Site, Seattle, Washington, United States

ImClone Investigational Site, Madison, Wisconsin, United States

Contact Details

Name: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Affiliation: Eli Lilly and Company

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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