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CEL-SCI to Present at Rodman & Renshaw 9th Annual Healthcare Conference
Date:10/30/2007

VIENNA, Va., Oct. 30 /PRNewswire-FirstCall/ -- CEL-SCI Corporation (Amex: CVM) announced that Geert Kersten, Chief Executive Officer, will be presenting at the Rodman & Renshaw 9th Annual Healthcare Conference being held at the New York Plaza Hotel from November 5-7, 2007. The presentation will be focused on its Phase III cancer product Multikine(R) which is the first biotech cancer product seeking to become a new first line standard of care treatment in cancer.

Mr. Kersten's presentation will be on Wednesday, November 7th, at 1:40 p.m. EDT. The presentation will be webcast live with slides and archived for 90 days after the conference. The webcast can be accessed at http://www.wsw.com/webcast/rrshq12/cvm or http://www.cel-sci.com.

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 of three and a half years following surgery. The U.S. Food and Drug Administration (FDA) gave the go-ahead for a Phase III clinical trial with Multikine in January 2007 and granted orphan drug status to Multikine in the neoadjuvant therapy of squamous cell carcinoma (cancer) of the head and neck in May 2007.

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

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

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


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SOURCE CEL-SCI Corporation
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