|  |   |  |  | Callisto Pharmaceuticals Announces Dr. Moshe Talpaz
			    to Join Scientific Advisory Board NEW YORK--(BUSINESS WIRE)--Oct. 21, 2003--Callisto Pharmaceuticals,
			  Inc.  (OTCBB: CLSP
			  - News) announced that Dr. Moshe Talpaz, Chairman
			  of the Department of Bioimmunotherapy of The University of Texas
			  M. D. Anderson Cancer Center has become a member of Callisto's
			  Scientific Advisory
			  Board.
  Dr. Talpaz, well known for his role in the clinical
			    development of Gleevec, is an internationally-recognized authority on
			    leukemia
			    and blood cancers. Dr. Talpaz continues to be involved in the
			    clinical development of numerous cancer drugs, and has been a pioneer
			    in developing
			    currently
			    accepted treatment protocols especially in the leukemia area. "I am
			    pleased to be working with Callisto on the clinical development of Atiprimod
			    which represents a new non-classical therapeutic approach to the treatment
			    of multiple myeloma. This drug tackles key cellular signals that drive this
			    terrible disease" says Dr. Talpaz. "We at Callisto are delighted
			    to have someone of Dr. Talpaz's experience and stature on our Scientific
			    Advisory Board. Dr. Talpaz brings a world of knowledge in designing and
			    running clinical trials, something that will be pivotal to us as we move
			    forward with our lead drug candidate, Atiprimod, into the clinic." says
			    Dr. Gary S. Jacob, CEO of Callisto Pharmaceuticals, Inc. 
  About Callisto Pharmaceuticals, Inc. Callisto is a biopharmaceutical company primarily focused on
			          the development of drugs to treat multiple myeloma, osteolytic
      bone disease and other cancers. Callisto's lead drug candidate, Atiprimod,
			          is
			    a small-molecule,
			    orally available drug with antiproliferative and antiangiogenic
			    activity. Atiprimod successfully completed Phase I clinical trials
			          in rheumatoid arthritis
			    patients and Callisto filed an IND on September 23, 2003 with
			          the U.S. Food and Drug Administration on Atiprimod to enter
      a Phase
			          I/IIa clinical
			    trial
			    in multiple myeloma patients. The drug is also being explored
			          as an agent to treat osteolytic bone disease. In addition,
      Callisto has programs
			    focused
			    on the development of an analog of the human intestinal hormone,
			    uroguanylin, to treat colon cancer, and drugs to protect against
			          staphylococcal and streptococcal
			    bioweapons, as a protection against the devastating effects of
			    toxic shock syndrome. Callisto has two operating subsidiaries,
			          Callisto Research Labs,
			    LLC and Synergy Pharmaceuticals Inc.
  Included in this release are "forward-looking: statements. Such statements
			    are indicated by words such as "expect," "should," "anticipate" and
			    similar words indicating uncertainty in facts and figures. Although
			    Callisto believes that the expectations reflected in such forward-looking
			    statements
			    are reasonable, it can give no assurance that such expectations
			    reflected in such forward-looking statements will prove to have been correct.
			    Callisto's
			    actual results could differ materially from those anticipated in
			    the forward-looking statements as a result of various factors. 
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