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Bad Luck or Bad Management: What’s Next For Bristol-Myers?
Just when they thought it
was safe to emerge from the debacle called ImClone Systems (NASDAQ:
IMCL), management at Bristol-Myers Squibb (NYSE: BMY) has stumbled
again…and again. With blockbuster drugs losing their patents faster than
Bill Clinton dropping his drawers, all the major pharmaceutical companies
are in search of the drug development grail.
In late March, however,
BMY was forced to reveal that a new study of a drug for the treatment of
heart failure, Vanlev, found that the drug was only marginally better than
a generic version of Merck’s (NYSE: MRK) blockbuster, Vasotec.
News of the results sent BMY’s share price down by 15% to a four-year
low.
Credibility, or lack of
it, is the number issue now at the company. During the course of the
development of Vanlev, investors had expected the drug to be BMY’s next
blockbuster, with annual sales of $1.0 to $2.0 billion at its peak.
Obviously, this will not come to pass, and management had to spend a few
days wiping the egg from its face.
The news that Vanlev
performed well in studies of 25,000 patients with hypertension, or high
blood pressure, however, did little to sway investors. The bottom line is
that even good news will be met with skepticism given the series of
miscues.
Just 10 days after the
Vanlev announcement, BMY had to reveal that wholesale inventories of its
medicines are too high in the U.S. and that reducing them will hurt
earnings in 2002. But the "hurt" may be up to a 40% decline this
year from earnings in 2001, and this coming from a company that was once
considered a star. The 15% share price drop would have been much worse if
the shares had not already lost so much ground in the past few months.
The problem is that with
so many blunders recently, it is impossible to determine if there is
anything else that might pop up, and with this many troubles, the
likelihood is that management does not have a good enough grasp on
operations to have an answer. BMY’s CEO, Peter Dolan, stated, "I
have taken a hard look at our business and have concluded that we must
improve our current operating performance, our cost structure, and our
focus on bringing great drugs to the market in the near term." Rocket
science this is not, and one would have expected something a bit more
profound.
The fact that he is also
"assuming direct responsibility" for BMY’s global
pharmaceutical business, in addition, to his chairman and CEO duties, does
not instill a greater sense of confidence in the company.
One also has to question
where the Board of Directors has been over the past six months. Obviously,
its oversight responsibilities have been lacking. But the directors are
probably going to have a busy time in the months ahead, as takeover rumors
immediately hit the market with BMY’s latest disclosures and the
resulting plunge in equity value. If there had been just one or two
mistakes, shareholders might stand by management and weather the current
storm. But given the circumstances, investors will most likely take any
reasonable premium that is offered above current price levels.
With 1.9 billion shares
outstanding, however, few companies have the financial wherewithal for a
$70 billion to $100 billion price tag. The possible names bandied about so
far include Pfizer (NYSE: PFE), Merck, Johnson & Johnson
(NYSE: JNJ), GlaxoSmithKline (NYSE: GSK), Pharmacia (NYSE:
PHA) and Novartis (NYSE: NVS). A hostile bid would require cash,
and that is a long shot, but bankers are probably already crunching the
numbers for their clients, smelling a huge fee in the current M&A
market drought. Apparently, one research analyst has estimated that at a
price of $50 per share, JNJ’s earnings per share would rise by 2% in
2003 without factoring in any cost savings, but would jump by up to 17%
with savings factored in, if it bought BMY. There has been no comment from
JNJ.
Our guess is that no one
will want to make a hostile bid, and Mr. Dolan will not be very receptive
to a friendly merger, preferring to turn the company around himself
instead of admitting defeat after less than a year at the helm. After all,
many decisions in business are based on ego and not sound business
judgement. On the other hand, there would appear to be little reason to
sell the company, absent a significant premium to the severely discounted
current price. If there are no more surprises, there is a good possibility
that BMY will remain independent; one more bombshell, however, and the
vultures won’t be circling, they will be dining.
BMY Is Not Alone
Unfortunately,
Bristol-Myers has some good company with regard to problems. In late
March, Watson Pharmaceuticals (NYSE: WPI) announced that the FDA
rejected the company’s Oxytrol skin patch for overactive bladders, but
requested additional information on the product. Because of the delay, WPI
revised the company’s financial outlook for 2002, lowering revenue
estimates $30 million to $50 million for the year. Sometimes there is a
silver lining, and because of the delay, significant launch expenses will
also be postponed, resulting in an increase in earnings per share this
year of $0.05 to $0.10.
In a profit warning
similar to BMY’s, Genzyme Corp. (NASDAQ: GENZ) announced that it
will reduce wholesale inventories of its flagship drug, Renagel, which is
used in kidney dialysis. The inventory levels will be lowered from 12
weeks to six weeks, resulting in a one-third drop in first quarter
earnings per share estimates. Sales of Renagel are expected to approach
$280 million in 2002, after more than tripling in 2001. Although sales of
the drug will not be impacted by the inventory reductions, investors took
GENZ’s share price down 10% on the news.
Finally, ViroPharma
(NASDAQ: VPHM), a development-stage pharmaceutical company focusing on new
antiviral medicines, disclosed that an FDA advisory panel recommended
against approval of the company’s new treatment for the common cold.
While the panel found that the drug, Picovir, did reduce the length of a
cold by one day, it had some serious side effects. VPHM’s share price
plunged by 59% on the news, and then dropped further to a 52-week low of
$3.56 per share, compared to a high a year ago of $41.00 per share (ouch).
The shareholder lawsuits
have already been filed, but management may have a big financial headache
looming. Aventis SA (NYSE: AVE) paid the company $25 million for
marketing rights to Picovir, but $20 million of it may have to be refunded
if certain milestones are not reached. FDA approval certainly is an
important milestone. One executive at ViroPharma said, "This drug is
not dead." Perhaps, but it may be awhile before it leaves the ICU.
The company has no other drugs in late stage development.
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