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Newly Published Clinical Data of Oral Cancer Drug REVLIMID Demonstrates Survival

This Site:en.yinlu.net Source:en.yinlu.net Writer: Time:2007-11-22
BRUSSELS, Belgium--(BUSINESS WIRE)--The European Myeloma Platform (EMP) welcomes new research published in this weeks New England Journal of Medicine which found that previously treated multiple myeloma patients who received REVLIMID with dexamethasone had an unprecedented nearly three year median survival rate the longest median survival ever observed in Phase III trials of this patient group. In addition to increased overall survival, the findings from the two large, U.S. and international clinical trials found that patients who received the oral cancer therapy in combination with the steroid dexamethasone also had increased response rates, time-to-disease progression and duration of response compared to patients treated with the steroid alone.

The EMP is excited by the potential impact that novel therapies, such as REVLIMID, are having on the treatment of multiple myeloma patients, said Dr. Rolf Pelzing, Chairperson, EMP, From personal experience, I can testify to the positive benefits of REVLIMID for patients. The EMP hopes that ongoing research, like these major international trials, will help to further the understanding of multiple myeloma and enable healthcare providers to have the necessary tools to turn the disease into a chronic, manageable condition.

Multiple myeloma is a rare form of cancer of plasma cells. It is the second most common cancer of the blood, affecting over 80,000 people in Europe and an estimated 750,000 worldwide at any one time. Although once considered a disease of the elderly, multiple myeloma is increasing in incidence and being diagnosed among younger people with half of the patients diagnosed today being younger than 60.

REVLIMID (lenalidomide) from Celgene is the newest of what are called the novel therapies which have changed the outlook for myeloma patients and are helping patients live longer with a better quality of life. REVLIMID has been approved in combination with dexamethasone for patients who have received at least one prior therapy in the U.S. and Europe.

EMP participated in meetings with the EMEA in advance of the European approval to represent the interests of myeloma patients and is continuing to work with local regulatory agencies to help secure local approval and reimbursement. EMP is working closely with the International Myeloma Foundation (IMF) and is striving to educate and empower myeloma patients across Europe.

EMP is a European umbrella organization of myeloma patient support groups. In accordance with the spirit of its basic motive, Patients for Patients, it is the only pan-European myeloma patient organization that is run by patients and their relatives for other patients.

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