Callisto Notified by American Stock Exchange of Acceptance of Plan of Compliance and Extension to Regain Compliance With Standar
29 1월 2007 - 11:00PM
PR Newswire (US)
NEW YORK, Jan. 29 /PRNewswire-FirstCall/ -- Callisto
Pharmaceuticals, Inc. (Amex: KAL; FWB: CA4), a developer of new
drug treatments in the fight against cancer and other major health
threats, today announced that the staff of the American Stock
Exchange ("AMEX") has reviewed the Company's plan of compliance to
meet the AMEX's continued listing standards and will continue the
Company's listing while the Company seeks to regain compliance with
Section 1003 (a)(iv) during the period ending April 3, 2007 and
Section 1003 (a)(i) during the period ending April 3, 2008. As
previously announced, on October 3, 2006 the Company received
notice from the AMEX staff indicating that the Company was below
certain of the Exchange's continued listing standards due to
guidelines set forth in sections 1003(a)(iv) and Section 1003(a)(i)
of the AMEX Company Guide. The Company will be subject to periodic
review by the AMEX Staff during the plan period. Failure to make
progress consistent with the plan or to regain compliance with the
continued listing standards by the end of the extension periods
could result in the Company being delisted from the AMEX. About
Callisto Pharmaceuticals, Inc. Callisto is a biopharmaceutical
company focused on the development of new drugs to treat various
forms of cancer and other serious afflictions. Callisto's drug
candidates in development currently include anti-cancer agents in
clinical development, in addition to drugs in pre-clinical
development for other significant health care markets, including
ulcerative colitis. One of the Company's lead drug candidates,
Atiprimod, is in development to treat advanced carcinoid cancer, a
neuroendocrine tumor, and relapsed multiple myeloma, a blood
cancer. Atiprimod is presently in a Phase II clinical trial in
advanced carcinoid cancer patients, and in Phase I/IIa human
clinical trials in relapsed or refractory multiple myeloma
patients, and advanced cancer patients, respectively. Another
anti-cancer drug, L-Annamycin, is being developed as a treatment
for forms of relapsed or refractory acute leukemia, a currently
incurable blood cancer. Callisto initiated a clinical trial of
L-Annamycin in adult relapsed or refractory acute lymphoblastic
leukemia patients in 4Q 2005. L-Annamycin, a new compound from the
anthracycline family of proven anti-cancer drugs, has a novel
therapeutic profile, including activity against resistant diseases
and significantly reduced cardiotoxicity, or damage to the heart,
compared to currently available drug alternatives. Callisto also
has drugs in preclinical development for gastro-intestinal
inflammation, and cancer. Callisto has exclusive worldwide licenses
from AnorMED Inc. and M.D. Anderson Cancer Center to develop,
manufacture, use and sell Atiprimod and L-Annamycin, respectively.
Callisto is also listed on the Frankfurt Stock Exchange under the
ticker symbol CA4. More information is available at
http://www.callistopharma.com/. Forward-Looking Statements Certain
statements made in this press release are forward-looking. 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 be correct. As discussed in the Callisto
Pharmaceuticals Annual Report on Form 10-K/A for the year ended
December 31, 2005, and other periodic reports, as filed with the
Securities and Exchange Commission, actual results could differ
materially from those projected in the forward-looking statements
as a result of the following factors, among others: uncertainties
associated with product development, the risk that products that
appeared promising in early clinical trials do not demonstrate
efficacy in larger-scale clinical trials, the risk that Callisto
will not obtain approval to market its products, the risks
associated with dependence upon key personnel and the need for
additional financing. DATASOURCE: Callisto Pharmaceuticals, Inc.
CONTACT: Dan D'Agostino of Callisto Pharmaceuticals, Inc.,
+1-212-297-0010, ext. 227, Web site: http://www.callistopharma.com/
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