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


To: Anthony Wong who wrote (536)11/13/1998 12:06:00 PM
From: Anthony Wong  Respond to of 2539
 
Corporate Bonds: Monsanto Plans to Sell $2.5 Billion of Bonds

Bloomberg News
November 13, 1998, 10:52 a.m. ET

New York, Nov. 13 (Bloomberg) -- Monsanto Co., a large
agricultural biotechnology companies, plans to sell $2.5 billion
of bonds, joining a growing list of companies taking advantage of
low interest rates and strong investor demand for bonds.

Monsanto, which will use proceeds of its sale to refinance
debt stemming from recent seed company acquisitions, follows
eight other sales of $1 billion or more in the past two weeks,
including $5 billion by Sprint Capital Corp.'s on Tuesday.
Several companies have returned to the market within days of
selling bonds. US West Capital plans to sell $400 million of 20-
year bonds, one day after affiliate US West Communications Inc.
sold $320 million of 10-year notes.

The flurry of sales, and efforts by corporate treasurers to
sell new bonds at lower spreads over Treasuries or outstanding
bonds, is beginning to take its toll on investors.

''The street wrung a lot of value out of some of these new
deals,'' said Richard Stevens, who helps manage $12 billion of
fixed-income assets at Colonial Advisory Services in Boston. If
that continues, some new bonds may sell slowly, he said. ''We may
start to see things come back with more spread to it,'' he said.

St. Louis-based Monsanto, which makes genetically improved
crops, drugs and nutritional products, outlined plans yesterday
to raise $5 billion through equity and debt sales, after spending
$8 billion the past two years to buy seed companies and other
technology it needed to compete in that market. The company said
it also plans to cut as many as 1,000 jobs and sell some
businesses for $1 billion.

Monsanto Ratings

The company's senior debt is rated ''A1'' by Moody's
Investors Service and is under review for possible downgrade.
It's rated ''A'' by Standard & Poor's Corp., with a negative
outlook.

The flurry of corporate bond sales the past month followed a
period of slack investor demand from early August to early
October. Buyers were concerned that a slowdown in the U.S.
economy would hurt corporate profits and credit ratings, and were
also deterred as securities dealers cut-back their market-making
as they were hit by trading set-backs and learned of bigger-than
expected holdings at troubled hedge funds.

Investor demand improved after the Federal Reserve's cut
short-term interest rates in late September and Oct. 15 boosted
investor confidence in the economy.

The spread between investment-grade corporate bonds and
Treasuries narrowed 15 basis points to about 163 basis points
since Oct. 15, according to
a Merrill Lynch & Co. index.

US West Capital, the finance arm of Denver-based telephone
company US West, plans to sell its 20-year bonds at an expected
yield of about 110 basis points more than 30-year Treasuries.

US West Communications, part of the former US West Inc.
family, sold $320 million of 10-year notes yesterday at a yield
of 5.672 percent, or 83 basis points more than Treasuries.
Earlier this year the old US West was split into two independent
companies: a telephone company known as US West Inc. (whose major
subsidiary is US West Communications), and cable media company,
MediaOne Group Inc.

Among other expected sales, Occidental Petroleum Corp., an
oil and gas exploration company, plans to sell between $300 million and $400 million of notes. KN Energy Inc., a natural gas producer and transporter, plans to sell $375 million of three-year notes next week.

--Kathleen Spillane in the New York newsroom (212) 318-2034/mq



To: Anthony Wong who wrote (536)11/13/1998 12:08:00 PM
From: Anthony Wong  Respond to of 2539
 
ACR MEETING: Celebrex Relieves Arthritis Pain As Well As NSAIDs

SAN DIEGO, CA -- Nov. 13, 1998 -- Results from Phase III studies of Searle
and Pfizer's investigational drug Celebrex™ (celecoxib) show that the drug
relieved the signs and symptoms of arthritis as effectively as the full therapeutic
dose of two of the most widely-prescribed non-steroidal anti-inflammatory
(NSAID) pain relievers, but with a gastrointestinal (GI) safety profile similar to
placebo.

The results were presented at the American College of Rheumatology's 62nd
national scientific meeting.

Celebrex is currently undergoing priority review by the United States Food and
Drug Administration for the treatment of the signs and symptoms of osteoarthritis
(OA) and rheumatoid arthritis (RA) and for the management of pain.

In one of the largest clinical development programs in arthritis, celecoxib was
tested in more than 14,000 patients and subjects world-wide.

Celebrex is a member of a proposed new class of agents known as specific
COX-2 inhibitors, which are designed to block the COX-2 enzyme activated in
inflammation while sparing the activity of the COX-1 enzyme that protects the
lining of the GI tract. The COX-1 enzyme also plays a role in blood clotting and
kidney functions. Common side effects of NSAIDs, which are non-specific
inhibitors of COX-1 and COX-2, include GI ulceration and bleeding, inhibition
of platelet aggregation and interactions with other drugs.

In clinical studies, celecoxib was as effective as the widely-used NSAID
naproxen in both RA and OA, but with a superior GI safety profile. One of the
Phase III studies, a 12-week trial involving 1,149 RA patients in an active
disease (flared) state, showed that celecoxib (100 mg, 200 mg, 400 mg BID)
was as effective as naproxen (500 mg BID) in relieving joint tenderness, pain and
swelling and was superior to placebo.

In addition, the upper GI safety profile of celecoxib was not significantly different
than placebo and was superior to naproxen.

Another 12-week study involving 1,004 patients with OA showed that celecoxib
(100 mg or 200 mg BID) worked as well as naproxen (500 mg BID) in relieving
OA symptoms and better than placebo. In a different trial, celecoxib at 600 mg
BID had no effect on platelet aggregation while naproxen at a full therapeutic
dose (500 mg BID) reduced platelet aggregation by 95 percent.

In another study, celecoxib worked as well as the widely-used NSAID
diclofenac, but with significantly fewer GI complaints and a four-fold reduction in
ulcers as detected by endoscopy. This 24-week double blind study involving
more than 600 RA patients demonstrated that, over the course of therapy,
celecoxib (200 mg BID) was as effective in the treatment of pain and swelling of
RA as diclofenac SR (75 mg BID).

Post-study endoscopic exams found the incidence of gastroduodenal ulcers was
nearly four times lower in celecoxib patients than those treated with diclofenac.
The overall incidences of GI complaints (for example, diarrhea, abdominal pain,
dyspepsia) were 33 percent higher in the diclofenac group than in the celecoxib
group.

In addition, more patients were able to continue taking celecoxib than diclofenac.
This was due to a higher number of withdrawals based on adverse GI events in
the diclofenac group. The Phase III study findings also showed that celecoxib
showed no significant drug interaction when taken with methotrexate or warfarin
-- two drugs often prescribed to arthritis patients.