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


To: Bull-like who wrote (429)11/27/1998 1:46:00 PM
From: Anthony Wong  Respond to of 642
 
Lilly (Eli) & Co. Reiterated 'Buy' at Gruntal

Bloomberg News
November 25, 1998, 10:00 a.m. ET

Princeton, New Jersey, Nov. 25 (Bloomberg Data) -- Lilly (Eli) & Co. (LLY
US) was reiterated ''buy'' by analyst David F. Saks at Gruntal & Co.
The 12-month target price is $108.00 per share.

-- Donna McDonald in Princeton, New Jersey, (609)279-3731



To: Bull-like who wrote (429)11/27/1998 1:52:00 PM
From: Anthony Wong  Respond to of 642
 
Bull, glad you're back to the Bull World from the Mouse World!

<LLY reached the 90 bucks target, now what? >

$108, apparently, after a bit of consolidation. Evista sales improving, no bad news...that would be enough.



To: Bull-like who wrote (429)12/2/1998 9:55:00 PM
From: Anthony Wong  Respond to of 642
 
Lilly's Evista Reduces Risk of Spine Fractures, Study Indicates

Bloomberg News
December 2, 1998, 4:34 p.m. ET

Lilly's Evista Reduces Risk of Spine Fractures, Study Indicates

Indianapolis, Dec. 2 (Bloomberg) -- Eli Lilly & Co. said a
study indicates its bone-protecting drug Evista reduces the risk
of spine fractures in older women, a finding that may help Lilly
in its effort to turn the pill into a blockbuster drug.

Lilly, the world's 10th largest drugmaker, introduced Evista
in January. Lilly needs new products to offset the loss of patent
in a few years on its antidepressant Prozac. Prozac made up 30
percent of Lilly's 1997 revenue of $8.52 billion.

In a study of more than 7,000 women, about 6 percent of
those given Evista developed spine fractures. Of those given
placebo, 10 percent developed them. Spine fractures are one of
the first signs of thinning of the bones. The fractures help
cause the hump or hunching of the back seen in some older women.

This study, which will continue, is only part of the work
Lilly must do to make Evista a challenger to Merck & Co.'s
similar drug, Fosamax.

''Evista has to kick in because Prozac is going to lose its
patent as some point,'' said Hemant Shah, an independent drug
analyst. ''It's going to be difficult to show effectiveness over
Fosamax.''

Shares of Lilly, based in Indianapolis, fell 1 3/8 to 88
7/8.

Merck's three-year-old Fosamax had sales of $540 million as
of September, up from 1997 sales of $532 million. Introduced in
January, Evista has had sales of about $82 million, disappointing
Lilly and investors.

Evista is approved in the U.S. only for the prevention of
thinning of the bones, a condition known as osteoporosis. The
U.S. Food and Drug Administration has approved Merck's Fosamax
for both prevention and treatment of osteoporosis. To seek a
similar FDA approval, Lilly is conducting these fracture studies.

Lilly presented its research today at a medical conference
in San Francisco for doctors specializing in bone disorders.
Merck and other rival drugmakers also will present research at
this meeting of the American Society for Bone and Mineral
Research. The conferences allow drugmakers to promote their
products to doctors.

Multiple Benefits

The key for making Evista a blockbuster for Lilly will be
showing that the drug has several benefits, such as reducing
breast-cancer risk as well as protecting bone, Shah said. Lilly
will present data at a meeting in San Antonio next week from its
research into use of Evista to prevent breast cancer.

Lilly also is studying whether Evista can help prevent heart
disease in older women.

Evista is the first of a new class of drugs that have been
called ''estrogen light.'' While Merck's drug treats bones,
Lilly's offers some of the benefits of estrogen with fewer side
effects.

Evista appears to work by acting on some of the body parts
estrogen helps, such as bones and the heart. Its chemical shape,
though, may block estrogen in the uterus and the breast. Long-
term use of estrogen may be linked to breast cancer.

Similar Products

Other drugmakers are trying to make similar products.
SmithKline Beecham Plc has a drug in the last of three stages of
testing required to apply for FDA approval. Pfizer has two likely
compounds for its 'estrogen light' drug. It intends to put the
better of these two into the last stage of testing last year
needed to apply for U.S. Food and Drug Administration approval.

These drugs also don't have some of the benefits of
replacement estrogen therapy, such as easing symptoms of
menopause.

--Kerry Dooley in the Princeton newsroom (609) 279-4016 /mfr



To: Bull-like who wrote (429)12/3/1998 8:26:00 PM
From: Anthony Wong  Read Replies (1) | Respond to of 642
 
Lilly Falls as Study Fails to Show Drug Curbs Hip, Wrist Breaks

Bloomberg News
December 3, 1998, 4:31 p.m. ET

Lilly Falls as Study Fails to Show Drug Curbs Hip, Wrist Breaks

Indianapolis, Dec. 3 (Bloomberg) -- Eli Lilly & Co. fell 5.8
percent after research failed to show its new drug Evista, used
to prevent thinning of bones in older women, could prevent hip
and wrist fractures.

Lilly, the world's 10th largest drugmaker, fell 5 1/8 to 83
3/4.

Indianapolis-based Lilly needs to build Evista and other new
products into blockbusters before it loses patent protection on
its top-seller, the antidepressant Prozac in a few years. Prozac
made up 30 percent of Lilly's 1997 revenue of $8.52 billion.

Research presented today at a medical conference showed no
significant difference between Evista and placebo in reducing hip
and wrist fractures, Lilly said. Other data has indicated the
drug may reduce spine fractures.

Merck's three-year-old Fosamax had sales of $540 million as
of September, up from 1997 sales of $532 million. Introduced in
January, Evista has had sales of about $82 million, disappointing
Lilly and investors.

Evista is approved in the U.S. only for the prevention of
thinning of the bones, a condition known as osteoporosis. The
U.S. Food and Drug Administration has approved Merck's Fosamax
for both prevention and treatment of osteoporosis. To seek a
similar FDA approval, Lilly is conducting these fracture studies.

Lilly presented its research today at a medical conference
in San Francisco for doctors specializing in bone disorders.
Merck and other rival drugmakers also will present research at
this meeting of the American Society for Bone and Mineral
Research. The conferences allow drugmakers to promote their
products to doctors.

--Kerry Dooley in the New York newsroom (212) 318-2300 /mfr



To: Bull-like who wrote (429)12/7/1998 1:13:00 PM
From: Anthony Wong  Read Replies (1) | Respond to of 642
 
Eli Lilly to Pay Up to $90 Mln to Develop, Sell Sepracor Antidepressant

Bloomberg News
December 7, 1998, 12:10 p.m. ET

Lilly Buys Sepracor Rights to New Version of Prozac (Update4)

(Adds analyst and company comment, updates shares.)

Indianapolis, Dec. 7 (Bloomberg) -- Eli Lilly & Co. said it
bought the rights from Sepracor Inc. for a successor to Lilly's
best-selling drug Prozac, moving to hold onto its market
leadership after Prozac loses patent protection.

Lilly, the world's 10th-largest drugmaker, will pay as much
as $90 million plus royalties for Sepracor's R-fluoxetine, a
version of Prozac that could have fewer side effects such as loss
of sex drive or impotence.

Sepracor's compound has patent protection until 2015 and
could help Lilly stave off generic competition for Prozac, which
had sales of $793 million in the third quarter and accounted for
about 30 percent of Lilly's 1997 sales. Patents on the nearly 11-
year-old antidepressant begin expiring after 2001.
''It's a silver bullet for Lilly's Prozac problem,'' said
Erick Lucera, an analyst with Independence Investment Associates,
which holds about 721,000 shares of Sepracor, an unprofitable
biotechnology company that specializes in developing purified
versions of best-selling drugs.

Shares of Marlborough, Massachusetts-based Sepracor were
unchanged at 88 at midday, after trading as high as 98
before U.S. markets opened. Shares in Indianapolis-based Lilly
rose 1/8 to 86 1/4.

Lilly will pay Sepracor an initial $20 million and as much
as $70 million in additional payments depending on the
antidepressant drug's progress in development, and will pay an
undisclosed royalty on sales of the product.

Prolonging a Patent

''This is good news for both of them,'' said Michael
Sheffery, an analyst with Orbimed Advisors. ''Sepracor is
providing a service for the industry that is clearly needed in
terms of prolonging a patent. For Lilly it affords them another
option for dealing with year X and the Prozac patent
expiration.''

Lilly said it expects to submit a marketing application to
the Food and Drug Administration for the new version of the anti-
depressant drug by 2001. Sepracor has said it expects Lilly's
patents to hold until June of 2004, and is aiming to get the new
version of the drug on the market by 2002.

The immediate hurdle for Lilly, though, could be defending
Prozac against generic competition long enough to get the new
version well established, according to independent analyst Hemant
Shah. While Lilly's patents begin to expire in 2001, the company
will face the first challenges to its Prozac empire much sooner.

Fighting Generic Drugmaker

Lilly and generic drugmaker Barr Laboratories Inc. are
expected to begin a trial next month on Barr's attempt to make a
generic version of Prozac.

Barr has been successful in winning the right to sell
generic versions of successful drugs, such as tamoxifen, Shah
said.

Still, a Barr victory in court likely would not mean
immediate sales of a generic Prozac, Shah said. If Barr wins,
then Lilly will appeal, he said. ''The whole court battle could
take two to three years,'' said Shah, who rates Lilly
''attractive.''

Lilly also needs to demonstrate the new version is an
improvement on Prozac and lower priced generic versions of it,
said Sidney Wolfe, director of Public Citizen's Health Research
Group, a Washington-based consumer watchdog group.

Otherwise, Wolfe said, ''they are doing something that is
going to keep the price inflated in this country to the
deteriment of people who may need the drug and may not be able to
afford'' the brand-name version.

Sepracor, founded in 1984, has discovered how to strip out
the side effects from drugs, including Prozac and Schering-Plough
Corp.'s antihistamine Claritin, by reformulating them to separate
active compounds from those that cause unwanted side effects.

Sepracor Shares Gain

Sepracor shares have more than doubled in the last year as
the company works on reformulating the top four allergy drugs as
well as two of the most popular asthma drugs.

Sepracor has an agreement with Johnson & Johnson to develop
a safer version of J&J's $1 billion Propulsid heartburn drug,
which can cause fatal heart rhythms. The company is nearing
approval for its Xopenex asthma drug -- a purified version of the
widely prescribed albuterol asthma medication. Sepracor is also
working on versions of Claritin and J&J's Hismanal.

The company already has one reformulated drug on the market:
Allegra, a safer version of the Hoechst AG's antihistamine drug
Seldane. The two companies are in a dispute over which one first
came up with the new formulation and Sepracor is not due to
receive any royalty payments on the drug before 2001.

With the Lilly agreement, ''you get another big drugmaker
and that adds credibility'' for Sepracor, Lucera said.

Lock and Key

Drugs such as Claritin and Prozac are made of ''twinned''
mirror-image sub-compounds, called isomers. While the active
isomer fits like a key into a molecular lock to produce a drug's
benefit, the mirror image isomer is like a key with the grooves
on top. At best, that means it won't fit the lock and is
inactive. At worst, it might fit an unintended lock and cause
side effects.

Big drugmakers, in their eagerness to bring new products to
market, skipped separating and patenting the individual isomers.

Sepracor develops versions that contain only a single
isomer, and licenses them back to the drugs' originators, and
they are now seeking regulatory approval to begin selling them.

The Food and Drug Administration has pushed big drugmakers
to start using the purifying technology, Sheffery said.

''It provides not only patent extension, it can also
eliminate troubling side effects,'' he said.

While Prozac carries certain side effects such as the
potential for impotence and loss of sex drive, it's not believed
to pose a health hazard to users. Still, Sepracor's drug ''has
the potential to provide treatment benefits in a broader range of
patients and for a broader range of indications than most
currently available antidepressants, including Prozac,'' Lilly
said.

-- Kristin Reed in Washington (202) 624-1858 with reporting by