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


To: Dan Spillane who wrote (1774)3/22/1999 8:03:00 PM
From: Bindusagar Reddy  Read Replies (1) | Respond to of 2539
 
Merril Lynch put out a positive report and DLJ raised estimates BUY rating and very positive comments. DLJ says that their Roundup sales for Q1 are better than expected. They raised their 1999 estimates to 1.00 from 80c and raised 2000 estimates to 1.40 from 1.20.

Merril Lynch praised the company referring to earlier than expected ANNUAL REPORT by Monsanto today posted on the WEB. He praised the company as they are executing their plan well in all the business segments. THE REPORT is available with pictures on WWW.MONSANTO.COM.

Merril report came at 5.30 EST and DLJ at 4.30 EST after market close. This should help the stock this week to push in to 50+.

BR



To: Dan Spillane who wrote (1774)3/22/1999 8:31:00 PM
From: Anthony Wong  Respond to of 2539
 
03/22 19:46 Merck <MRK.N> launching pain drug Vioxx in Mexico

MEXICO CITY, March 22 (Reuters) - U.S. pharmaceutical giant Merck and
Co. Inc. said on Monday that Mexico would be the first market where its
new pain reliever Vioxx would be available with its launch here this week.

"Mexico will be the first country in the world to have Vioxx available," a
statement from the company's Merck Sharp and Dohme unit said. It said
Mexican health authorities approved the drug on Feb. 1.

Vioxx is one of a new line of pain relievers known as Cox-2 inhibitors
designed to treat pain and arthritis without the gastrointestinal side effects
often seen in aspirin and ibuprofen.

Brisk initial U.S. sales of G.D. Searle & Co's <MTC.N> Cox-2 inhibitor,
Celebrex, have put it on track to top Pfizer Inc. <PFE.N> impotency drug
Viagra as the most successful drug launch ever.

Vioxx is due to be reviewed by a U.S. Food and Drug Administration
advisory committee in April, with approval expected this spring.
Germany's Boehringer Ingelheim also has a Cox-2 drug expected to be
approved in the U.S. late this year.

moneynet.com@NEWS-P1&Index=0&HeadlineURL=../News/NewsHeadlines.asp&DISABLE_FORM=&NAVSVC=News\Company



To: Dan Spillane who wrote (1774)3/22/1999 9:58:00 PM
From: Anthony Wong  Respond to of 2539
 
Roundup Ready Yields Lag
Soybean Digest
Vol. 59, No. 5, Mid-March, 1999

by Syl Marking

Roundup Ready (RR) soybeans have turned in some
whopper yield performances, like topping 90 bu/acre in
one Ohio State University variety performance test in
'98.

But extensive research data now strongly suggest there is, on average, a small yield
lag with this new technology.

Data from more than 3,000 side-by-side comparisons from 40 university
performance tests conducted across eight states in 1998 were summarized by Ed
Oplinger, University of Wisconsin extension agronomist.

Here are the results:

Average yields of RR varieties ranged from 14% less to 13% more than
conventional varieties.

When averaged across all tests, RR varieties were 4% lower in yield than
conventional varieties. That would be a 2-bu/acre difference on a 50-bu/acre
yield.

When averaged across all locations, the top five RR varieties yielded 5% less
than the top five conventional varieties in 200 comparisons.

Harry Minor, a University of Missouri extension agronomist, made similar
comparisons in his state and came up with about the same yield lag - 1.6 bu/acre. In
some comparisons he made of Group V beans from Arkansas and Mississippi, there
was about a 5% yield lag with RR varieties.

Oplinger adds that another University of Wisconsin study used so-called sister lines
- very similar genetics with the RR gene in one of the matched pairs. The yield
difference in favor of the conventional varieties was 4-6%.

This yield lag factor for RR soybeans has been mentioned by many scientists and
top-end growers who made side-by-side comparisons since 1996, when these
transgenic varieties were first commercialized. And it was mentioned in each of
Soybean Digest's Special Reports on Herbicide-Tolerant Crops since 1996.

Oplinger and Minor think this potential yield difference is fully realized by scientists
and most progressive growers with yield monitors, especially if they have
side-by-side comparisons.

"In the industry, breeders know that they don't have yield parity with Roundup
Ready varieties yet," Minor declares.

The most heard explanation for the yield lag is that the RR gene often has not been
put into the most elite lines that some companies offer. A more plausible
explanation, say some soybean breeders, is that in the rush to get RR lines on the
market, many companies have not made enough backcrosses to capture all of the
yield potential in the parent lines.

"The breeders have been caught with trying to turn things out as quickly as
reasonably possible to stay competitive," says Oplinger.

In either case, the conventional wisdom says that will be corrected in a reasonably
short time, and yield lags will be eliminated.

"I don't see any reason not to have yield parity in the future with this technology,"
says Minor.

Oplinger and Minor don't think average soybean growers realize or believe that
there is a yield lag, on average, for RR varieties. Or if the growers do, they do not
care because of the ease and effectiveness of the weed control they've gotten.

Oplinger points out that about a million acres of RR beans were grown in 1996.
That increased to 9 million in '97 and over 25 million acres in '98.

"Therefore, if performance is to be measured by grower acceptance, then RR
soybean varieties have certainly performed well," says Oplinger. "Also, the use of
these varieties has solved some major weed problems for some growers."

Veteran weed scientists can't recall any herbicide product launch that created the
excitement and acreage explosion that RR soybeans created. And grower surveys
by Monsanto continue to show extremely high grower satisfaction. Postharvest
surveys of RR soybean growers showed that nearly nine of 10 plan to grow some
RR soybeans in 1999. With hundreds of new RR varieties available, Monsanto
officials expect RR acreage to increase again this year.

In university variety performance trials, weed control has to be virtually perfect in
order to measure true genetic yield potential of varieties, Minor points out. For
average growers, weed control on larger acreages is not always that good,
especially if weather problems occur.

"A farmer may lose the potential yield advantage of good conventional varieties if
he doesn't have real good weed control. And if he has weeds he has not been able
to effectively control with conventional herbicide programs, then he should give the
Roundup Ready system serious consideration. That's because he is likely to lose
more due to poor weed control than to the possible yield lag with the Roundup
Ready system."

Oplinger urges growers to take a pencil to all the factors, including the yield lag,
herbicide costs, technology fee, etc. Then figure out any bottom-line differences for
their operations.

So, what's the take-home message of all of this?

If you are going to grow RR soybeans, study the variety performance tests from
your state university, private companies or farms to try to pick the highest-yielding
RR varieties with the defensive packages needed for your farm. If you don't, you
could be sacrificing maximum yield for ease of weed control.

"We have identified some Roundup Ready varieties, both from a yield and defensive
package stand point, that growers definitely ought to consider," Oplinger concludes.
"There is information out there to pick those varieties that best fit your needs - and
your bottom line."

homefarm.com




To: Dan Spillane who wrote (1774)3/22/1999 10:01:00 PM
From: Anthony Wong  Respond to of 2539
 
Patent paralysis

With hundreds of patent applications from every
biotechnology seed/chemical company jamming the
patent office, duplicate claims are made.
Unfortunately, these interferences can slow the
flow of products to you, cause companies to risk
investment loss, and create higher seed prices to
cover climbing legal costs.

by Dale McDonald
Farm Industry News
Vol. 32, No. 6, Mid-March, 1999


(Second in a series - Who owns nature?)

Since the earliest days of the biotechnological revolution, commercialization has
been plagued by delay.

First, it took years to get approval for the initial field tests of genetically altered
crops. Then, environmental activists tried to stop the technology cold with a series
of lawsuits. When the test plots finally did get planted, saboteurs literally pulled
some experiments up by the roots.

More than a decade later, the turtle rather than the hare still defines this burgeoning
technology. But today the perpetrator of postponement is none other than the Patent
and Trademark Office (PTO) of the U.S. government. The office is overwhelmed,
understaffed, short of funds and years behind the times.

To be fair, the current backlog in the patent office that is stifling technological
advancement did not come about by design; it happened by default. Four situations
at the PTO underscore the problem.

Speed is not a priority. When an applicant files for a patent, nothing happens until
the application is reviewed and the PTO issues what is called a first office action.
Once that first office action is issued, the applicant has six months to respond.
Typically, a series of office actions must be dealt with. Although the applicant is
required to meet a response timetable, no such requirement is made of the PTO.
Applicants are on the clock; the PTO is not.

Eventually, the PTO issues a final office action. If the applicant disagrees with this
action, he or she has to amend, appeal or refile and start the process all over again.
During this phase, time is measured in years, not months.

Interferences truly interfere. Virtually all commercial biotechnology companies
currently have hundreds of patent applications sitting at the PTO, and of course
many of them overlap. Because of this, "interferences" have become a large part of
the process.

Ken Loertscher, general patent council at Dow AgroSciences explains: "What I find
is that things are really hung up in the interference proceedings. It's a hearing at the
PTO to determine who has rights to obtain the U.S. patent when two or more
parties are essentially claiming the same thing.

"Interference proceedings are very technical, very involved, and there are a lot of
requirements for paperwork. We still have an application we filed in 1983 that is in
interference. That is not unusual. Another aspect is that some parties may have an
interest in tying things up even if they know they will eventually lose."

The system can be manipulated. Parties often file "submarine" patent
applications that are unethical, mean-spirited and designed purely to manipulate the
system for profit. And these applications are not uncommon.

Rick Shear, associate general counsel for intellectual property at Monsanto, says,
"The submarine tactic is filing a patent application, then intentionally doing whatever
you can to keep it pending - for years - until such time as someone else, who has
never seen the patent, produces an invention. Then bang, the [submarine] patent
issues and they've got you. It's a problem."

Herb Jervis, vice president and chief intellectual property council at Pioneer
Hi-Bred International, agrees: "[The submarine tactic] stems from the fact that
patents are secret until they issue. If the process was open and the information was
made public at application rather than issuance, [the tactic] would be stopped.

"I think people do try to profit on another person's research by dragging out the
patent process for a commercial objective. They file intentionally sketchy
disclosures, wait for someone else to develop the technology, then jump out with a
patent. And by doing that, they could put a smaller company out of business," Jervis
says.

Too little, too late. Recently, the acting commissioner of the PTO announced that
his office would hire 2,100 new patent examiners over the next three years. It
sounds impressive, but there's a catch. Those who routinely deal with the patent
office say it takes three or four years for a new examiner to become competent -
especially if he or she is assigned to handle complex technologies like biotechnology.

Industry sources admit they don't exactly help the situation. It's a common practice
for companies to hire the best patent examiners away from the PTO. The
companies gain insider information and technical competence, but they also weaken
the very talent pool they depend on.

Although the institutional bottlenecks slow down the system, efforts to patent
"expressed sequence tags" (ESTs) threaten to bring the patent process to a halt.
ESTs are gene fragments that, once identified, can help isolate and identify entire
genes. In that sense they are used simply as tools, and their patentability is
controversial for two reasons: A flood of hundreds or even thousands of EST patent
applications would paralyze the PTO, and patents granted for tags could hinder
commercialization efforts.

One corporate executive who asked not to be identified had this to say: "The
patentability of ESTs needs to be determined quickly because they already are
causing problems for any company trying to commercialize a product. With so many
of these patents pending, you just have to hope that you aren't infringing on a patent
that has yet to be issued. It's a real quagmire and could affect every company's
freedom to operate."

Opinions vary, but nearly everyone agrees that trouble is on the horizon. Monsanto's
Shear says, "In general, Monsanto's position is that everything should be patentable.
But having said that, if someone discovers an EST and doesn't really know its
function, then later I come along and at great expense discover the full-length gene,
I shouldn't have to worry about that former EST patent. Right now, we have to
worry because we don't know how the patent office or the courts are going to
handle it. Ultimately, it probably comes down to the courts."

George Jen, senior patent attorney at Novartis, says, "ESTs are very controversial.
If an EST can be shown to be homologous to an entire gene, that meets the PTO's
utility standard. You have to identify the strand and demonstrate what it can be used
for. The other issue is that filing for thousands of sequences does drag the system
down. That type of filing is simply a defensive strategy. Still, ESTs and their scope
have yet to be litigated."

Their scope is what concerns Col Seccombe, CEO of Garst Seed. He says, "In
Europe they do not allow you to patent an EST. But it appears that in the United
States you will be allowed to isolate the fragment and patent it on the basis that it
has a useful purpose, and the useful purpose is fishing out the rest of the gene.

"The problem is that someone else comes along and discovers the gene and
determines, for example, that it's useful in controlling drought resistance. Then this
company with all the EST patents says, 'We own a piece of that gene, therefore you
can't use it without paying us a royalty.' It looks like every discovery made in the
next 20 years could prompt four people to put their hands up and say, 'I own a piece
of that.' Then you go from interference hearings to court case after court case. Is
this the direction we want this technology to take?"

Obviously, there are more questions about the patent process than answers. Even
so, the patent office - and Congress - could take a number of actions to further
define the direction this technology takes:

Particularly with ESTs, determine precisely what is patentable and what is
not. And do it sooner, not later.

Reduce uncertainty by requiring the patent application to be published early -
not years later upon issuance. In Europe, applications are published within 18
months.

Make every effort to streamline the appeals and interference proceedings.

During the normal application process, put a clock on the PTO examiners. If
the process takes too long, add that time back onto the patent when it's
issued. Changing the patent award from 17 years after issuance to 20 years
from application date was only a first step.

Compensate top patent examiners at the industry's pay scale. That would
neutralize the allure of using the PTO as a training ground for a company's
patent lawyers.

Institute an appeals format when a patent issues that would include any
party's arguments against the patent. Make the hearing public, and make the
ruling final. That would reduce litigation, which is epidemic.

Until the system of determining intellectual property rights is refined, this technology
will continue to be held hostage. And over the long term, many experts say refining
the system is simply not enough.

Writing in the Harvard Business Review, Lester Thurow, professor of management
and economics at MIT, says, "The prevailing wisdom among those who earn their
living within our system of intellectual property protection is that some minor
tweaking here and there will fix the problem. The prevailing wisdom is wrong. The
time has come not for marginal changes but for wide-open thinking about designing
a new system from the ground up."

Whether it's a new system or an improved system that emerges, the current state of
affairs is troubling to those trying to make headway today.

Monsanto's Shear says, "It takes a lot of time and money to push a product from
research to commercialization. And there are failures along the way. When our
business managers look at potential products, they want to know if we are
protected. But with all these patent applications sitting around...it's just really
uncomfortable."

Look for Part III of "Who owns nature?" in the next issue of Farm Industry News.

homefarm.com



To: Dan Spillane who wrote (1774)3/22/1999 10:04:00 PM
From: Anthony Wong  Respond to of 2539
 
When crops save lives
homefarm.com

I'm not sure whether I had already posted this in early March. No harm reading it again.



To: Dan Spillane who wrote (1774)3/22/1999 11:13:00 PM
From: Anthony Wong  Read Replies (2) | Respond to of 2539
 
Editorial BIOTECHNOLOGY The sound of science
St. Louis Post-Dispatch
Posted: Monday, March 22, 1999 | 4:35 a.m.

Webster Groves building contractor Steve Cassilly is strolling down
the aisles of a natural foods store, checking out labels. His ritual is
designed to avoid biologically engineered food additives and
genetically altered vegetables.

Nearby, scientists at Monsanto, the world leader in genetic food
technologies, spend endless hours and a lot of money researching
and testing what they say are improved, safe methods of food
production - which happen to be the very foods Mr. Cassilly is
trying to avoid.

These two scenes are the extremes of the important international
debate on the scientific, health, cultural and political implications of
biotechnology.

Mr. Cassilly and the Monsanto scientists may have already staked
out their positions in the this high-tech battle about the future of
food. Mr. Cassilly is a spokesman for a citizens group that wants
Congress to require labeling of biologically altered products.
Monsanto insists that these products are safe.

But most of the public is starved for information. A new study by
the National Academy of Sciences may help answer some of the
questions posed by biotechnology.

So far, much of the public discussion has been based on fear
rather than facts. That is partly because a great deal of the
supporting science comes from the labs and researchers at
biotechnology companies, like Monsanto. These companies stand to
make big profits if their technologies are successful. Therefore,
consumers have some reason to exercise skepticism.

But consumer decisions, government regulations and international
trade agreements should be made on the basis of sound scientific
studies. The National Academy of Sciences promises to be a
rational, independent voice in the chorus of debate on
biotechnology. No set of findings will be the final word on any
scientific topic. But the National Academy of Sciences study will
carry tremendous influence in shaping public policy.

Two signals from the Academy indicate the urgency for the
information. First, the Academy is paying for the study from its
endowment. Nine times out of 10, Academy studies are requested
by, and funded by, Congress or some other government agency.

Second, most studies take at least 18 months. But the Academy has
accelerated this study, hoping to complete it in six months.

The Academy also deserves credit for understanding that the
implications of genetically engineered foods reach beyond labs and
farm fields. Tampering with food supplies, and how they are
grown, can affect everything from the social fabric of farm life in
Southern Illinois and rural Missouri, to the political stability of
agriculture-based economies overseas. The Academy's study will
include a look at social and economic implications, as well as
scientific questions of safety and health.

In an atmosphere where the public is starved of sound science, the
National Academy of Sciences study could help move us past fear
to facts.

stlnet.com