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Biotech / Medical : Biotech Valuation -- Ignore unavailable to you. Want to Upgrade?


To: Biomaven who wrote (5055)12/6/2001 1:45:46 PM
From: Shawn Donahue  Read Replies (2) | Respond to of 52153
 
Peter,

Sorry that I didn't check to see if it was posted on this thread earlier. I had just found it the other day, while researching articles that discuss IMCL, and I thought that even if it was posted earlier, it might be a nice reminder for some biotech investors on how to get earlier information from medical research organizations...

<<On IMCL, the short answer is to look at what BMY paid for their share of the drug. A pharma doesn't lay out in excess of $1b for a drug that hasn't yet been approved without first doing a lot of homework>>

I don't know if the below analyst reads your 'Biotech Valuation' thread or not, but he seems to agree with your "short answer" on why IMCL is $70+ a share: <g>

Thank you,

Shawn

NeoPharm, Inc. (Nasdaq: NEOL) New Report Sees BMY/Imclone Transaction As Bullish


NEW YORK, Dec. 4 /PRNewswire/ -- The recent $2 billion investment by Bristol-Myers Squibb (NYSE: BMY) in Imclone Systems (Nasdaq: IMCL) reflects an escalation in Big Pharma interest in (and prices paid for) late-stage cancer compounds. As an industry leader in cancer drug delivery systems with six of its own oncology compounds in human clinical trials, few biopharmaceutical companies have more to gain than NeoPharm.

This is the main conclusion of a research recently published by Melhado Flynn & Associates, Inc. and written by portfolio manager/analyst, D. H. Talbot, who manages a limited partnership that invests mainly in small-cap medical technology stocks. NEOL is one of his largest holdings.

Mr. Talbot has decided to share his research with others because he regards current Wall Street coverage as inadequate. He expects 2002 to be an especially good year for the stronger biotech and related stocks. He further estimates that the NEOL share price will surpass the old high ($39) over the next 12-months, owing mainly to interest in 2 compounds.

1) LEP (liposomal encapsulated paclitaxel). Earlier this year, Street

analysts were estimating that NeoPharm's stake in future LEP earnings

had a present value of roughly $70 per share. Talbot believes LEP

remains on course -- perhaps slightly behind the original time line for

potential FDA approval but well ahead in terms of potential label

indications vis-a-vis BMY's Taxol(R). NEOL's partner, Pharmacia, has

called LEP the biggest oncology drug in its R&D pipeline.

2) IL13-PE38 (a novel "smart bomb" compound for brain cancer). There is

presently no known cure for malignant glioma which is diagnosed in

approximately 17,500 people in the U.S. each year and claims roughly

the same number of lives. NeoPharm recently announced early Phase I/II

efficacy data which remarkably showed, in some cases, a complete

response despite relatively low dosage levels and with only minor

adverse reactions noted. If these results are confirmed in further

trials, Talbot estimates that IL13-PE38 could gain FDA approval by 1Q

of 2003 -- at least a year before LEP.

The report estimates that IL13-PE38 could generate $4.00-5.00 per share in U.S. earnings within 2 years of launch, off of projected domestic sales of $200 million. (The large EPS impact is due in part to the fact that NeoPharm has only 16m shares outstanding). Talbot's projections do not take into account possible use of IL13 for treating renal cell cancer.

With the exception of historical information, the matters discussed in this document include forward-looking statements that involve a number of risks and uncertainties. Investment performance is subject to significant uncertainties and contingencies beyond the control of Melhado Flynn & Associates, Inc. Any significant change can materially affect future results. Actual results could differ significantly from the forward-looking statements in this document.

This material, and any opinions expressed, are for informational purposes only and constitute neither a prospectus nor a solicitation of orders for the purchase or sale of any security. Health/Vest Advisors, Melhado, Flynn & Associates, Inc. and/or its officers and directors may, at times, have a position in the shares of NeoPharm, Inc.

Melhado Flynn & Associates, Inc. is a member of the National Association of Securities Dealers, CRD number 7340.

MAKE YOUR OPINION COUNT - Click Here

tbutton.prnewswire.com

SOURCE D. H. Talbot

CO: Melhado Flynn & Associates, Inc.; NeoPharm, Inc.; Bristol-Myers Squibb; Imclone Systems

ST: New York

IN: FIN

SU: RTG

12/04/2001 10:30 EST prnewswire.com



To: Biomaven who wrote (5055)1/4/2002 11:00:54 AM
From: Shawn Donahue  Read Replies (1) | Respond to of 52153
 
Peter,

<<On IMCL, the short answer is to look at what BMY paid for their share of the drug. A pharma doesn't lay out in excess of $1b for a drug that hasn't yet been approved without first doing a lot of homework.>>

Below is an article on Drug Giants with an update on IMCL;
and Bristol-Myers Squibb $B investment...do you have any insight into what might happen next?

Thanks in advance,

Shawn

Pharmaceuticals
Drug Giants Show Their Achilles Heels
Matthew Herper, Forbes.com, 01.02.02, 5:35 PM ET

NEW YORK - Last September, ImClone Chief Executive Samuel Waksal boasted that his company's new cancer fighter would be "one of the biggest drugs in the history of oncology." Bolstering that audacious claim, drug giant Bristol-Myers Squibb dropped $2 billion securing the rights to the drug, dubbed Erbitux, and making an investment in ImClone.

So it came as a bit of a shock on Dec. 28 when the Food and Drug Administration rejected the new drug application that ImClone (nasdaq: IMCL - news - people) submitted for Erbitux. The rejection is maybe just a delay, meaning the FDA wants more data than ImClone provided. But the delay is surprising given the weight Bristol-Myers (nasdaq: BMY - news - people) threw behind the drug.

Then again, Bristol probably felt some level of desperation--and that had to make Erbitux, a great drug in the first place, look even better than it is.
Bristol-Myers is in the middle of a massive turnaround. It has sold or spun off its orthopedics and consumer divisions and pledged to focus intensely on its core drug business, which it enlarged with the purchase of DuPont's (nyse: DD - news - people) pharmaceuticals division.

The only problem is that, although Bristol has been putting together an impressive pipeline, it's facing a period in which it can't promise investors much growth: Patent expirations are approaching on Glucophage, a diabetes treatment with more than $1 billion in sales; BuSpar, an anti-anxiety drug that was once a blockbuster; and its famous cancer drug, Taxol.

Similar problems have plagued Merck (nyse: MRK - news - people), one of the biggest losers in the Dow for 2001. Patent expirations led the Whitehouse Station, N.J.-based giant, which had drug sales of $21 billion in 2001, to warn of flat earnings in 2002. In six months, it could lose $4 billion in annual sales, as five aging drugs lose the last of their patent protection due to cheaper generics. Cholesterol fighter Zocor, which Merck expects to have 2002 sales of more than $1 billion, will lose exclusivity four years later.

Merck has some of the best research laboratories in the drug business, and those labs have churned out a host of neuroscience drugs to replace Merck's fabled heart drugs, which are also losing patent protection. Unfortunately, growth from new drugs does not always line up with the hemorrhaging that results as older drugs lose patents and are exposed to generic competition.

If drug companies are going to rely on blockbusters, the massive growth that results from a new drug pipeline may inevitably be followed by growth droughts, as drug stables age and go off patent. When a drug worth billions of dollars loses almost all of its value, it's going to hurt, no matter how good a company's pipeline or how big the drug.

Right now, the best-armored battleship in the drug business is Pfizer (nyse: PFE - news - people). But that armor is partly a result of the age of its stable of drugs. Lipitor, a $6.5 billion cholesterol fighter and currently the world's biggest drug, and Norvasc, an antihypertension drug, don't face patent expirations for several years. At Pfizer's annual analyst meeting last December, CEO Hank McKinnell said he doesn't think Pfizer will have to face patent expirations until 2006-2007.

That means that, to some extent, the patent droughts are an issue not of if, but of when. Is there any alternative? Maybe. While Merck was one of the Dow's worst performers, Johnson & Johnson (nyse: JNJ - news - people) was one of its best. Although J&J relies on drugs for much of its growth, it is also big in areas like medical devices--including its much-vaunted re-entry into stents, which are used to re-open clogged arteries.

But for its diversity, Johnson & Johnson pays with massive complexity--it has 195 operating divisions in 51 countries. Other drug firms will likely rely on trying to have enough blockbusters to keep the ball rolling, as Bristol-Myers does. Unfortunately, that probably means that, like Bristol, they will face the occasional patent drought.
forbes.com