SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Strategies & Market Trends : How To Write Covered Calls - An Ongoing Real Case Study!

 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext  
To: Douglas Webb who wrote (4952)9/22/1997 8:01:00 PM
From: Herm   of 14162
 
Here is some news. The company HAS NOT posted a profit yet. They may be getting close. The company does trade options. The open interest is VERY WEAK and only 2% of the company is held by institutions. The current stock price has skyrocketed and without positive earnings it's doubtful the price can be sustained at current levels. The data distorted the RSI and Bollinger Bands by the extreme price swings. Lots of speculation! It may be worth keeping an eye on the stock. It's a bit risky for my IRA. I would pass for other sure hits like BTGC or VVUS. I hate to lose money and time! SAN RAMON, Calif., Sept. 4 /PRNewswire/ -- SuperGen, Inc. (Nasdaq: SUPG & SUPGW), an emerging pharmaceutical company, today announced it has acquired exclusive worldwide rights to a patented anti-cancer compound from the Stehlin Foundation for Cancer Research Houston, TX) in exchange for an up-front payment of SuperGen common stock valued at $2.5 million, ongoing collaborative development payments, additional milestone equity payments and royalties on eventual product sales. The drug (a topoisomerase I inhibitor which has been designated "RFS 2000" by the company) is patented and is a semi-synthetic derivative of a naturally occurring plant alkaloid with cancer-killing properties. It is extracted from the bark and leaves of the camptotheca acuminata tree, which is native to China. RFS 2000 currently is in Phase II human trials for pancreatic cancer, for which Orphan Drug Status already has been obtained from the U.S. Food and Drug Administration. As compared to rates observed with the standard treatment, in clinical trials conducted to date RFS 2000 has shown marked improvement in survival rate and quality of life, even in late-stage patients. At therapeutic dosages, adverse effects in these patients appear to be minimal. While the company initially will focus on accelerating clinical development for pancreatic cancer, the agreement grants SuperGen worldwide rights to RFS 2000 for all indications. Like Taxol(R), in various animal tumor models, RFS 2000 has anti-tumor effects in a number of solid tumors, including breast, lung, ovarian, melanoma and colorectal. However, unlike Taxol(R), RFS 2000 can be given orally and the company believes has a much more favorable safety profile. It is estimated that there were more than 100,000 new cases of pancreatic cancer in the world in 1996. Because pancreatic cancer cannot be diagnosed until the late stages of the disease, it is regarded as one of the most difficult cancers to treat, and it is the fourth leading cause of all cancer deaths. Fewer than 20% of all patients diagnosed with pancreatic cancer survive for more than one year. "We believe RFS 2000 is a breakthrough compound for pancreatic and many other cancer patients," said Dr. Joseph Rubinfeld, SuperGen's Chairman and Chief Executive Officer. "We believe that for many companies, RFS 2000 could by itself be the platform for a successful oncology business. SuperGen is committed to establishing the leadership position in oncology with marketed products like Nipent(R), our medium-term Extra(TM) formulations of existing anti-cancer drugs, and RFS 2000. Through collaborations with cutting-edge research institutions like the Stehlin Foundation we will continue to build and maintain that leadership." "SuperGen is the perfect partner to move RFS 2000 through clinical development," said Dr. John S. Stehlin, Jr., Founder of the Stehlin Foundation. "SuperGen combines the level of senior management experience of a large pharmaceutical company with the drive and sense of urgency of an entrepreneurial biotechnology company." The Stehlin Foundation for Cancer Research at St. Joseph Hospital in Houston, Texas was founded in 1969, and since that time has had as its primary focus the discovery and development of new and improved anti-cancer drugs. Its research laboratory has the largest number of human tumors in storage in the world and has in the past supplied approximately 75% of the human tumors used by the National Cancer Institute in their testing with nude mice. The Stehlin Foundation pioneered the use of nude mice in cancer research, establishing a correlation between an anti-cancer drug's effectiveness on a human tumor implanted in a mouse and the drug's effectiveness in patients. Based in San Ramon, California, SuperGen is an emerging pharmaceutical company dedicated to the development and commercialization of products intended to treat life-threatening diseases, particularly cancer and blood cell disorders, as well as other serious conditions such as obesity and diabetes. SuperGen is developing an anti-cancer portfolio of proprietary and enhanced Extra (TM) products, and currently is marketing five drugs for the treatment of cancer patients. The company also currently is sponsoring human clinical trials for drugs targeting cancer, anemias, obesity and diabetes. This press release contains forward looking statements within the meaning of Section 21A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, and are subject to the safe harbors created thereby. Such statements, including the ongoing clinical development and commercialization of RFS 2000 and SuperGens goal of leadership in oncology involve certain risks and uncertainties associated with a development stage pharmaceutical company. Actual results could differ materially from those projected in the forward looking statements as a result of failure to obtain regulatory approval for RFS 2000 in pancreatic cancer, failure to establish clinical benefit for RFS 2000 in other indications and failure to obtain regulatory approval for other SuperGen products in the development phase, as well as other risk factors discussed in SuperGen's reports on file with the U.S. Securities Exchange Commission (including but not limited to the report on Form 10-Q for the quarter ended June 30, 1997). SOURCE SuperGen Inc. -0- 09/04/97 /CONTACT: Les Stickles of SuperGen, Inc., 510-327-0200, ext. 210/ (SUPG) CO: SuperGen Inc. ST: California IN: MTC CHM SU:
Report TOU ViolationShare This Post
 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext