MAXIM PHARMACEUTICALS PRESENTS PRECLINICAL DATA ON HISTAMINE´S ABILITY TO PREVENT LIVER DAMAGE

MAXIM PHARMACEUTICALS PRESENTS PRECLINICAL DATA ON HISTAMINE'S ABILITY TO PREVENT LIVER DAMAGE Results presented at the European Association for the Study of the Liver (EASL) SAN DIEGO, April 19, 2004 - Maxim Pharmaceuticals (Nasdaq: MAXM) (SSE: MAXM) announced preclinical results indicating that histamine may prevent lipopolysaccharide (LPS)-induced liver injury. The results were presented at the 39th annual European Association for the Study of the Liver (EASL) meeting in Berlin, Germany. In this preclinical study, LPS is used to increase the severity of alcohol-induced damage. These new results demonstrate the ability of histamine to prevent LPS-induced liver injury in a rodent model by showing efficacy when delivered in a manner mimicking oral administration. Maxim scientists have previously shown that histamine is protective against early alcohol-induced liver injury in rats. Histamine is known to inhibit reactive oxygen species and LPS-induced pro-inflammatory cytokines like TNF- in circulating inflammatory cell types in blood. Similar cells in the liver called Kupffer cells, also mediate inflammation by releasing pro-inflammatory cytokines when stimulated by LPS. Maxim researchers tested histamine in a rat model using alcohol in combination with a high-fat diet to create liver injury. LPS was administered as a "second insult" to dramatically increase damage and the markers that measure this damage. Subcutaneous histamine pre- treatment at all doses prevented serum transaminase (ALT, AST) levels from elevating compared to when LPS was given alone. When histamine was directly given into the intestine, a dose-dependent protection was achieved. Histamine also dose-dependently decreased LPS-induced TNF-? and IL-6 mRNA levels in the liver. "These continued results were used to support our oral histamine program now in phase 1 human trials and the continued understanding of histamine's mechanism of action in chronic liver diseases," says Kurt R. Gehlsen, Senior Vice President and Chief Scientific Officer. "This work will help to advance toward clinical trials of our oral product candidate in the treatment of chronic liver diseases including Hepatitis C, alcoholic liver disease (ALD) and non-alcoholic steatohepatitis (NASH)". Chronic liver diseases, including hepatitis, ALD and NASH, affect an estimated 25 million people in the U.S., approximately one in every ten. Hepatitis C is the leading blood-borne infection in the United States. The U.S. Center for Disease Control and Prevention estimates that over 4.5 million Americans are infected with the hepatitis C virus. The World Health Organization and other sources estimate that at least 200 million people are infected worldwide. Some experts estimate that without substantial improvements in treatment, deaths from hepatitis C will surpass those from HIV. Hepatitis C is the leading cause of liver cancer and the primary reason for liver transplantation in many countries. Even with recent advances, approximately half of patients still do not attain a sustained response with current therapies. NASH, non-alcoholic steatohepatitis, also called 'fatty liver,' is an inflammation of the liver associated with an increase of fat deposits in liver cells that may lead to severe liver damage and cirrhosis. NASH may occur in middle- aged, overweight, and often in diabetic patients who do not drink alcohol. ALD, caused by alcohol abuse, is one of the ten leading causes of death in the United States. Overview of Histamine Therapy Research has shown that oxygen free radicals released by certain immune cells can suppress the immune system and damage normal tissue, a process commonly referred to as oxidative stress. Oxidative stress, implicated in numerous diseases, is most pronounced in the liver and can damage or destroy liver tissue in patients with hepatitis and other chronic liver diseases. Histamine has been shown in preclinical testing to prevent the production and release of oxygen free radicals, thereby reducing oxidative stress. Accordingly, treatment with histamine has the potential to prevent or reverse damage induced by oxidative stress, thereby protecting critical cells and tissues, including the liver. Preclinical research, including results presented in 2003 at the annual meeting of the American Association for the Study of Liver Diseases (AASLD) and published in Inflammation (vol. 27 (5), p317-327), suggest that histamine can protect and promote the healing of the liver in models of ALD, NASH and partial surgical resection. Research regarding histamine dihydrochloride has been the subject of more than 80 presentations at major scientific and clinical meetings, and has been published in more than 300 scientific and clinical articles. Ceplene, Maxim's injectible form of histamine, has been tested in more than 17 trials in 2,000 patients, including hepatitis C patients. Maxim anticipates that any additional clinical testing of histamine for the treatment of chronic liver diseases will be with an oral formulation as in the completed Phase 1A trial announced today. A three-minute animation of the histamine mechanism of action in its injectible formulation as Ceplene(TM) can be viewed on the Company's website at www.maxim.com. Maxim Overview Maxim Pharmaceuticals is a global biopharmaceutical company with a diverse pipeline of therapeutic candidates for life-threatening cancers and liver diseases. Maxim's research and development programs are designed to offer hope to patients by developing safe and effective therapeutic candidates that have the potential to extend survival while maintaining quality of life. Maxim's lead drug candidate Ceplene (subcutaneously delivered histamine dihydrochloride) is designed to prevent or inhibit oxidative stress, thereby reversing immune suppression and protecting critical immune cells. In November 2003, Maxim filed an application for market authorization in Europe for approval to market Ceplene for the treatment of advanced malignant melanoma. Ceplene is currently being tested in Phase 3 cancer clinical trials for advanced malignant melanoma with liver metastasis and acute myeloid leukemia. Phase 2 trials of Ceplene are also underway for the treatment of hepatitis C and advanced renal cell carcinoma. In addition to Ceplene and oral-formulation histamine, Maxim is developing small-molecule inhibitors and activators of programmed cell death, also known as apoptosis, which may serve as drug candidates for cancer, cardiovascular disease and other degenerative diseases. Ceplene, the oral histamine formulation and the apoptosis inducers are investigational drugs and have not been approved by the U.S. Food and Drug Administration (FDA) or any international regulatory agency. This news release contains certain forward-looking statements that involve risks and uncertainties. Such forward-looking statements include statements regarding the efficacy, safety and intended utilization of Ceplene, the oral histamine formulation and the apoptosis inducers, and the conduct, results and timelines associated with the Company's clinical trials. Such statements are only predictions and the Company's actual results may differ materially from those anticipated in these forward-looking statements. Factors that may cause such differences include the risk that products that appeared promising in early research and clinical trials do not demonstrate safety or efficacy in larger- scale clinical trials and the risk that the Company will not obtain approval to market its products. These factors and others are more fully discussed in the Company's periodic reports and other filings with the Securities and Exchange Commission. Note: The Maxim logo is a trademark of the Company. Editor's Note: This release is also available on the Internet at http://www.maxim.com. ### Contacts: Larry G. Stambaugh Aline Schimmel (Investors) Chief Executive Officer Burns McClellan Anthony E. Altig (212) 213-0006 Chief Financial Officer Sean Collins (Media) (858) 453-4040 Valerie Bent (Media) CCG Investor Relations (818) 789-0100 ------------------------------------------------------------ This information was brought to you by Waymaker http://www.waymaker.net The following files are available for download: http://www.waymaker.net/bitonline/2004/04/19/20040419BIT00020/wkr0001.doc http://www.waymaker.net/bitonline/2004/04/19/20040419BIT00020/wkr0002.pdf