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CEL-SCI to Present at Rodman & Renshaw 9th Annual Healthcare Conference

Wednesday, October 31, 2007 General News
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VIENNA, Va., Oct. 30 CEL-SCI Corporation(Amex: CVM) announced that Geert Kersten, Chief Executive Officer, will bepresenting at the Rodman & Renshaw 9th Annual Healthcare Conference being heldat the New York Plaza Hotel from November 5-7, 2007. The presentation will befocused on its Phase III cancer product Multikine(R) which is the firstbiotech cancer product seeking to become a new first line standard of caretreatment in cancer.
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Mr. Kersten's presentation will be on Wednesday, November 7th, at 1:40p.m. EDT. The presentation will be webcast live with slides and archived for90 days after the conference. The webcast can be accessed athttp://www.wsw.com/webcast/rrshq12/cvm or www.cel-sci.com.
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About CEL-SCI's Phase III Cancer Drug Multikine:

In Phase II clinical trials Multikine was shown to be safe and well-tolerated, and to improve the patients' overall survival by 33% at a median ofthree and a half years following surgery. The U.S. Food and DrugAdministration (FDA) gave the go-ahead for a Phase III clinical trial withMultikine in January 2007 and granted orphan drug status to Multikine in theneoadjuvant therapy of squamous cell carcinoma (cancer) of the head and neckin May 2007.

Multikine, a patented defined mixture of naturally derived cytokines, isthe first immunotherapeutic agent in a new class of drugs called "ImmuneSIMULATORS." Immune SIMULATORS simulate the way our natural immune systemacts in defending us against cancer. As opposed to other immunotherapieswhich are designed to target a single or limited number of specific antigensor molecules, Immune SIMULATORS are multi-targeted; they simultaneously causea direct and targeted killing of the specific tumor cells and they activatethe immune system to produce a stronger anti-tumor attack on multiple fronts.

Multikine is also the first immunotherapeutic agent being developed as afirst-line standard of care treatment for cancer. It is administered prior toany other cancer therapy because that is the period when the anti-tumor immuneresponse can still be fully activated. Once the patient has advanced disease,or had surgery or has received radiation and/or chemotherapy, the immunesystem is severely weakened and is less able to mount an effective anti-tumorimmune response. Other immunotherapies are administered after the patient hasreceived chemotherapy and/or radiation therapy, which can limit theireffectiveness.

The Company has operations in Vienna, Virginia and Baltimore, Maryland.CEL-SCI's other products, which are currently in pre-clinical stage, haveshown protection against a number of diseases in animal tests and are beingtested against diseases associated with bio-defense and avian flu.

SOURCE CEL-SCI Corporation
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