CEL-SCI CORPORATION REPORTS THIRD QUARTER 2008 FINANCIAL RESULTS

VIENNA, VA, AUGUST 20, 2008 – CEL-SCI CORPORATION (AMEX: CVM) reports financial results for the three and nine months ending June 30, 2008.

The Company’s loss from operations for the quarter ended June 30, 2008 was $2,176,679 versus a loss of $3,776,263 during the same quarter in 2007. The Company’s loss from operations for the nine months ended June 30, 2008 was $7,129,215 versus a loss of $7,368,779 during the same nine months in 2007.

The net loss per common share for the quarter ended June 30, 2008 was $0.02 versus a net loss per common share of $0.05 during the same quarter in 2007. The Company’s net loss per common share for the nine months ended June 30, 2008 was $0.06 versus a net loss per common share of $0.10 during the same nine month period in 2007.

During the three month period ended June 30, 2008, research and development charges were $975,183 compared to $632,868 during the same period in 2007. During the nine month period ended June 30, 2008, research and development expenses were $3,041,212 compared to $1,817,891 during the same period in 2007.

During the three month period ended June 30, 2008, general and administrative expenses were $1,177,288 compared to $3,104,755 during the same period in 2007. During the nine month period ended June 30, 2008, general and administrative expenses were $3,931,857 compared to $5,473,605 during the same period in 2007.

Geert Kersten, Chief Executive Officer of CEL-SCI said, “We are moving forward just as we had planned. The greatest part of the expenditures are focused on completing the manufacturing facility and starting the Phase III study of our Multikine cancer drug. Some additional funds were spent on our new and very promising Rheumatoid Arthritis vaccine.”

About 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.

CEL-SCI is currently building a manufacturing facility for Multikine close to Baltimore, MD. Upon completion of the facility in the 3rd quarter of 2008, CEL-SCI will commence the Phase III clinical trial. Multikine appears to be the first non-toxic cancer drug.

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.