To: Miljenko Zuanic who wrote (128 ) 9/25/2000 9:33:44 AM From: scaram(o)uche Read Replies (1) | Respond to of 362 Monday September 25, 6:05 am Eastern Time Press Release Titan Announces Positive Results for Zomaril Phase III Clinical Trial in Schizophrenia SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--Sept. 25, 2000--Titan Pharmaceuticals (AMEX:TTP - news), today announced positive safety and efficacy data from a large scale, controlled, phase III study of Zomaril(TM) (iloperidone), a new drug currently in development for the treatment of schizophrenia. The global trial, conducted by Novartis (NYSE:NVS - news), involved more than 600 patients at more than 40 centers throughout the US, Europe, Canada, Australia and South Africa and was designed to assess the ability of Zomaril to control safely and effectively the positive and negative symptoms in schizophrenia patients. The results demonstrated that both dose levels of Zomaril used in the study achieved a highly statistically significant reduction in the symptoms of schizophrenia as assessed by the Brief Psychiatric Rating Scale. These findings were also supported by highly statistically significant improvements in the total score for the Positive and Negative Syndrome Scale with both dose levels. In addition, the study confirmed that Zomaril possesses an excellent tolerability profile with no extrapyramidal symptoms, little weight gain and no effect on serum prolactin. Full details of the study results will be presented at international psychiatry congresses next year. In announcing the results, Titan Chairman and CEO, Dr. Louis R. Bucalo, called these results very promising and stated, ``We are very excited about these results from the Novartis development program. With this recent progress, we are further encouraged that Zomaril may represent an important new option for patients with schizophrenia.'' In November 1997 Novartis Pharma AG entered into an agreement with Titan Pharmaceuticals for the rights to develop, manufacture and market Zomaril worldwide with the exception of Japan. The study is part of a Novartis program called `ReALIZe' (Research to Assess the Long-term Impact of Zomaril), which comprises seven different studies being conducted at some 300 centers around the world. To date, more than 3200 patients have participated in ReALIZe studies, which are designed to evaluate the safety and efficacy of Zomaril against various end-points. Titan Pharmaceuticals, Inc. is a biopharmaceutical company developing proprietary therapeutics for the treatment of central nervous system disorders, cancer and other serious and life-threatening diseases. The press release may contain ``forward-looking statements'' within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such statements include, but are not limited to, any statements relating to the Company's development program and any other statements that are not historical facts. Such statements involve risks and uncertainties, including, but not limited to, those risks and uncertainties relating to difficulties or delays in development, testing, regulatory approval, production and marketing of the Company's drug candidates, unexpected adverse side effects or inadequate therapeutic efficacy of the Company's drug candidates that could slow or prevent product markets, the uncertainty of patent protection for the Company's intellectual property or trade secrets and the Company's ability to obtain additional financing if necessary. Such statements are based on management's current expectations, but actual results may differ materially due to various factors, including those risks and uncertainties mentioned or referenced in this press release. Contact: Titan Pharmaceuticals, Inc, South San Francisco Louis R. Bucalo, M.D., 650/244-4990 or Ruder Finn, Inc., New York Investors: Wendi B. Green, 212/593-6374 or Media: Sarah O'Connell, 212/583-2724