SECURITIES AND EXCHANGE COMMISSION
                             WASHINGTON, D.C. 20549


                                    FORM 8-K


                                 CURRENT REPORT

                     Pursuant to Section 13 or 15(d) of the
                         Securities Exchange Act of 1934


        Date of Report (date of earliest event reported): October 9, 2001


                               CEL-SCI CORPORATION
                          ------ --------------------
             (Exact name of Registrant as specified in its charter)


     Colorado                         0-11503                  84-0916344
-------------------------------------------------------------------------------
(State or other jurisdiction    (Commission File No.)         (IRS Employer
of incorporation)                                           Identification No.)



                              8229 Boone Blvd. #802
                                Vienna, VA 22182
                -------------------------------------------------
          (Address of principal executive offices, including Zip Code)


       Registrant's telephone number, including area code: (703) 506-9460
                                                           --------------



                                       N/A
                 ----------------------------------------- ----
          (Former name or former address if changed since last report)



<PAGE>


Item 5. Other Events and Regulation FD Disclosure

On October 9, 2001 the Institute of Human Virology (IHV) at the University of
Maryland, Baltimore and CEL-SCI CORPORATION (AMEX: CVM) announced the
presentation of new clinical data for CEL-SCI's immunotherapy drug, Multikine,
at the Annual Meeting of the International Society for Interferon and Cytokine
Research in Cleveland, Ohio. These findings could lead to a new treatment for
HIV-infected women with HPV induced cervical dysplasia, the precursor to
cervical cancer. In the U.S. alone, approximately 120,000 to 140,000 women have
this disease and are in need of effective therapy.

At the conference it was reported that all five patients treated thus far at the
lowest dose in an ongoing dose escalating study showed clinical improvement by
colposcopic (stereoscopic, binocular magnification of the cervix under a focused
beam of light) examination. Three out of four patients had no evidence of
dysplasia on biopsy seven to eight weeks after the final injection. Biopsies on
the remaining volunteer showed no apparent changes in her dysplasia. One patient
was lost to follow-up. All of the patients tolerated the injections well and
without any associated serious adverse reactions. Enrollment at this dose level
is completed. The evaluation of Multikine at a higher dose is ongoing as a
preliminary to the initiation of a pivotal clinical trial in 2002.

The presentation is entitled, "Immunotherapy with Leukocyte Interleukin,
Injection for Human Papilloma Virus (HPV) Induced Cervical Dysplasia in HIV
Patients", and was authored by G. Taylor, L. Ely, C. Davis, O. Ioffe, E. Talor,
N. Khanna, R. Redfield, and E. Tramont at the Institute of Human Virology, the
University of Maryland, CEL-SCI Corporation and the National Institute of
Allergy and Infectious Diseases (NIAID). This study was supported in part by a
MIPS (Maryland Industrial Partnership) grant from the State of Maryland, a
program designed to foster cooperation between researchers/clinicians and
industry.

HPV infection is also a leading health problem in non-HIV-infected American
college age women. A large concern among women who have HPV-induced cervical
dysplasia is that the surgical procedures required to treat cervical dysplasia
have a high morbidity rate ranging from cervical incompetence to hysterectomy
and the inability to bear children. Furthermore, cervical cancer is the second
leading cause of cancer death in women worldwide.

Geert Kersten, Chief Executive Officer of CEL-SCI said, "The results we have
seen in this study have literally catapulted this disease to the forefront of
our development work. The reasons for this are as follows:

1)   We are seeing a high response rate in this very difficult to treat group of
     patients.

2)    The drug was well tolerated and the results were achieved without any
      associated serious adverse reactions related to Multikine. Given the
      fragile health of these HIV-infected women and past experiences with other
      drugs in this patient population, this is very important.

<PAGE>


3)    There is no effective therapy for these HIV/HPV co-infected women and we
      know of no other therapies currently in clinical development for this
      patient population.

4)    There are an estimated 120,000 to 140,000 HIV/HPV co-infected women in the
      U.S. alone whose needs are not adequately addressed. Co-infection with HPV
      is common in HIV-infected women and cervical cancer, which follows
      cervical dysplasia, is classified as an AIDS defining illness.

5)    We believe that HPV-induced cervical dysplasia patients who are also
      HIV-infected, and therefore are the most difficult to treat and cure, may
      represent the fastest way to bring our drug Multikine to the market."

Maximilian de Clara, President of CEL-SCI added, "The market for cervical
dysplasia is huge since millions of women are treated for it every year. For
this reason, there is a lot of clinical work ongoing in cervical dysplasia.
However, all of the agents under development are being developed in women who
have a competent immune system. CEL-SCI, on the other hand, will first focus on
those women who are immuno-compromised. There are also immuno-compromised groups
other than HIV-infected patients and we expect to get to those after we have
started a pivotal clinical trial in the HIV-infected population."

Multikine is a mixture of immune system regulators known as cytokines and
chemokines at near physiologic doses. One of the cytokines, Interleukin-2, is
widely used to treat cancer. Multikine has been tested in more than 150 cancer
patients and in 14 AIDS patients, to date, with only minimal side effects.

A center of the University of Maryland Biotechnology Institute, the Institute of
Human Virology was established in 1996 as a partnership between the State of
Maryland, the City of Baltimore, the University of Maryland System, and the
University of Maryland Medical System, to create and develop a world-class
center of excellence focusing on chronic viral diseases and virally-linked
cancers. The IHV is dedicated to discovery, research, treatment, and prevention
of these diseases and cancers. Its unique structure seeks to connect cohesive,
multidisciplinary research and clinical programs so that new treatments are
streamlined from discovery to patient. The IHV serves patients locally and the
scientific community globally.

CEL-SCI is developing new immune system based treatments for cancer and
infectious diseases. CEL-SCI has operations in Vienna, Virginia and Baltimore,
Maryland. CEL-SCI's web site can be found at www.cel-sci.com.

Forward Looking Statements

When used in this report, the words "intends," "believes," "anticipated" and
"expects" and similar expressions are intended to identify forward-looking
statements. Such statements are subject to risks and uncertainties which could
cause actual results to differ materially from those projected. Factors that
could cause or contribute to such differences include, an inability to duplicate
the clinical results demonstrated in clinical studies, timely development of any
potential products that can be shown to be safe and effective, receiving
necessary regulatory approvals, difficulties in manufacturing any of CEL-SCI's

<PAGE>

potential products, inability to raise the necessary capital and the risk
factors set forth from time to time in CEL-SCI's SEC filings, including but not
limited to its report on Form 10-K for the year ended September 30, 2000.
CEL-SCI undertakes no obligation to publicly release the result of any revision
to these forward-looking statements which may be made to reflect the events or
circumstances after the date of this report or to reflect the occurrence of
unanticipated events.


                                   SIGNATURES

      Pursuant to the requirements of the Securities Exchange Act of 1934, the
registrant has duly caused this report to be signed on its behalf by the
undersigned hereunto duly authorized.


Date:  October 11, 2001

                                 CEL-SCI CORPORATION



                                 By:  /s/ Geert R. Kersten
                                      ----------------------------------------
                                      Geert R. Kersten, Chief Executive Officer
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SECURITIES AND EXCHANGE COMMISSION
                             WASHINGTON, D.C. 20549

                                    FORM 8-K

                                 CURRENT REPORT

                     Pursuant to Section 13 or 15(d) of the
                         Securities Exchange Act of 1934

        Date of Report (date of earliest event reported): October 9, 2001

                               CEL-SCI CORPORATION
                          ------ --------------------
             (Exact name of Registrant as specified in its charter)

     Colorado                         0-11503                  84-0916344
-------------------------------------------------------------------------------
(State or other jurisdiction    (Commission File No.)         (IRS Employer
of incorporation)                                           Identification No.)

                              8229 Boone Blvd. #802
                                Vienna, VA 22182
                -------------------------------------------------
          (Address of principal executive offices, including Zip Code)

       Registrant's telephone number, including area code: (703) 506-9460
                                                           --------------

                                       N/A
                 ----------------------------------------- ----
          (Former name or former address if changed since last report)
Item 5. Other Events and Regulation FD Disclosure

On October 9, 2001 the Institute of Human Virology (IHV) at the University of
Maryland, Baltimore and CEL-SCI CORPORATION (AMEX: CVM) announced the
presentation of new clinical data for CEL-SCI's immunotherapy drug, Multikine,
at the Annual Meeting of the International Society for Interferon and Cytokine
Research in Cleveland, Ohio. These findings could lead to a new treatment for
HIV-infected women with HPV induced cervical dysplasia, the precursor to
cervical cancer. In the U.S. alone, approximately 120,000 to 140,000 women have
this disease and are in need of effective therapy.

At the conference it was reported that all five patients treated thus far at the
lowest dose in an ongoing dose escalating study showed clinical improvement by
colposcopic (stereoscopic, binocular magnification of the cervix under a focused
beam of light) examination. Three out of four patients had no evidence of
dysplasia on biopsy seven to eight weeks after the final injection. Biopsies on
the remaining volunteer showed no apparent changes in her dysplasia. One patient
was lost to follow-up. All of the patients tolerated the injections well and
without any associated serious adverse reactions. Enrollment at this dose level
is completed. The evaluation of Multikine at a higher dose is ongoing as a
preliminary to the initiation of a pivotal clinical trial in 2002.

The presentation is entitled, "Immunotherapy with Leukocyte Interleukin,
Injection for Human Papilloma Virus (HPV) Induced Cervical Dysplasia in HIV
Patients", and was authored by G. Taylor, L. Ely, C. Davis, O. Ioffe, E. Talor,
N. Khanna, R. Redfield, and E. Tramont at the Institute of Human Virology, the
University of Maryland, CEL-SCI Corporation and the National Institute of
Allergy and Infectious Diseases (NIAID). This study was supported in part by a
MIPS (Maryland Industrial Partnership) grant from the State of Maryland, a
program designed to foster cooperation between researchers/clinicians and
industry.

HPV infection is also a leading health problem in non-HIV-infected American
college age women. A large concern among women who have HPV-induced cervical
dysplasia is that the surgical procedures required to treat cervical dysplasia
have a high morbidity rate ranging from cervical incompetence to hysterectomy
and the inability to bear children. Furthermore, cervical cancer is the second
leading cause of cancer death in women worldwide.

Geert Kersten, Chief Executive Officer of CEL-SCI said, "The results we have
seen in this study have literally catapulted this disease to the forefront of
our development work. The reasons for this are as follows:

1)   We are seeing a high response rate in this very difficult to treat group of
     patients.

2)    The drug was well tolerated and the results were achieved without any
      associated serious adverse reactions related to Multikine. Given the
      fragile health of these HIV-infected women and past experiences with other
      drugs in this patient population, this is very important.
3)    There is no effective therapy for these HIV/HPV co-infected women and we
      know of no other therapies currently in clinical development for this
      patient population.

4)    There are an estimated 120,000 to 140,000 HIV/HPV co-infected women in the
      U.S. alone whose needs are not adequately addressed. Co-infection with HPV
      is common in HIV-infected women and cervical cancer, which follows
      cervical dysplasia, is classified as an AIDS defining illness.

5)    We believe that HPV-induced cervical dysplasia patients who are also
      HIV-infected, and therefore are the most difficult to treat and cure, may
      represent the fastest way to bring our drug Multikine to the market."

Maximilian de Clara, President of CEL-SCI added, "The market for cervical
dysplasia is huge since millions of women are treated for it every year. For
this reason, there is a lot of clinical work ongoing in cervical dysplasia.
However, all of the agents under development are being developed in women who
have a competent immune system. CEL-SCI, on the other hand, will first focus on
those women who are immuno-compromised. There are also immuno-compromised groups
other than HIV-infected patients and we expect to get to those after we have
started a pivotal clinical trial in the HIV-infected population."

Multikine is a mixture of immune system regulators known as cytokines and
chemokines at near physiologic doses. One of the cytokines, Interleukin-2, is
widely used to treat cancer. Multikine has been tested in more than 150 cancer
patients and in 14 AIDS patients, to date, with only minimal side effects.

A center of the University of Maryland Biotechnology Institute, the Institute of
Human Virology was established in 1996 as a partnership between the State of
Maryland, the City of Baltimore, the University of Maryland System, and the
University of Maryland Medical System, to create and develop a world-class
center of excellence focusing on chronic viral diseases and virally-linked
cancers. The IHV is dedicated to discovery, research, treatment, and prevention
of these diseases and cancers. Its unique structure seeks to connect cohesive,
multidisciplinary research and clinical programs so that new treatments are
streamlined from discovery to patient. The IHV serves patients locally and the
scientific community globally.

CEL-SCI is developing new immune system based treatments for cancer and
infectious diseases. CEL-SCI has operations in Vienna, Virginia and Baltimore,
Maryland. CEL-SCI's web site can be found at www.cel-sci.com.

Forward Looking Statements

When used in this report, the words "intends," "believes," "anticipated" and
"expects" and similar expressions are intended to identify forward-looking
statements. Such statements are subject to risks and uncertainties which could
cause actual results to differ materially from those projected. Factors that
could cause or contribute to such differences include, an inability to duplicate
the clinical results demonstrated in clinical studies, timely development of any
potential products that can be shown to be safe and effective, receiving
necessary regulatory approvals, difficulties in manufacturing any of CEL-SCI's
potential products, inability to raise the necessary capital and the risk
factors set forth from time to time in CEL-SCI's SEC filings, including but not
limited to its report on Form 10-K for the year ended September 30, 2000.
CEL-SCI undertakes no obligation to publicly release the result of any revision
to these forward-looking statements which may be made to reflect the events or
circumstances after the date of this report or to reflect the occurrence of
unanticipated events.

                                   SIGNATURES

      Pursuant to the requirements of the Securities Exchange Act of 1934, the
registrant has duly caused this report to be signed on its behalf by the
undersigned hereunto duly authorized.

Date:  October 11, 2001

                                 CEL-SCI CORPORATION

                                 By:  /s/ Geert R. Kersten
                                      ----------------------------------------
                                      Geert R. Kersten, Chief Executive Officer