 David Pyott
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Before Botox became a popular beauty treatment, Allergan was just a small ophthalmic business that made prescription eye therapies
and contact lens care products. But during a decade of off-label use-mostly in Hollywood as a quick fix for frown lines-Botox's
(botulinum toxin type A) sales grew and slowly transformed the company's focus and future. Last year, FDA approved the product
for cosmetic purposes, opening the door to consumer advertising, and its sales jumped 39 percent from the first quarter 2002
to the first quarter 2003.
But CEO David Pyott is quick to point out that Allergan is much more than a one-product cosmetic company. "Sixty percent of
the Botox business is, in fact, therapeutic," he says. "And last year, Botox was only a third of our total sales." With a
projected annual growth rate of about 23 percent during the next five years, a full pipeline, and a streamlined new focus,
Allergan's "future's so bright, you gotta wear shades," as the Timbuk3 song says. (See "Analysts' View," page 34.)
 At a Glance
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Eye Care Evolution The company's best strategic move-licensing botulinum toxin type A in the late 1980s-was reluctantly made. Alan Scott, an
ophthalmologist, had discovered that diluted doses of botulinum toxin were effective in treating eye spasms and founded a
small company called Oculinum. Scott obtained an FDA investigational new drug approval for the neuromodulator but needed a
partner to gain marketing approval. So he asked Allergan to take on its development. Company leaders had minimal interest
in the project, but two of its scientists saw possibilities and convinced them to run clinical trials. Allergan earned approval
to treat blepharospasm (uncontrollable blinking) and strabismus (crossed eyes) and took the toxin to market in 1989 under
the name Oculinum.
Around the same time, according to folklore, a Canadian ophthalmologist mentioned to her husband, a dermatologist, that her
patients' forehead wrinkles faded away after she injected the product around their eyes. Excited by the possibilities, together
they experimented on a nurse in their joint practice. The results were impressive. The couple then shared their discovery
with other doctors, some of whom were located in Hollywood, and the off-label cosmetic use mushroomed.
Meanwhile, Allergan bought Scott's company, renamed the product Botox, and gained approval in 11 countries by 1992. But the
company didn't start clinical trials for the cosmetic indication until 1997. Its leaders knew they needed to proceed carefully
with FDA, and they wanted to use data from independent studies to support their application. In 2002, Botox Cosmetic was approved
in the United States to treat glabellar lines, commonly known as frown lines. It is now marketed in 20 other countries for
that use, including France, which okayed it this year with the brand name Vistabel. France will act as the member reference
state for the European Union, and more approvals are likely to follow.
 David Pyott,
Up Close
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Over the years, the company gained global approval for the product for various conditions-eye muscle disorders, cervical dystonia,
and hyperhidrosis-and now sells Botox in more than 70 countries. In 2002, the product's sales hit $440 million, a 40 percent
increase from 2001. (See "Botox Bounty." ) But that's just the beginning. Pyott says, "It's no longer if, but when Botox will
be more than $1 billion."
But when he joined Allergan in January 1998 after a long career at Novartis, the Botox clinical trials had just begun, and
the company had been through a rough few years of losing patent protection on several ophthalmic products. He says, "The big
assumption of the late '80s, was that generics would never come to ophthalmic pharmaceuticals because the category was too
small. Bad, bad assumption." So the board of directors brought in Pyott to make some changes. He was only the third person
to lead the company, which at that time had been around for nearly 50 years.
And he'd been hired to cut expenses, so employees were uneasy, especially when he started closing manufacturing plants. "I
had worked in six countries in the last 20 years and whether I was talking to Spaniards or Germans or Americans, I'd say,
'Sorry guys, I'm Scottish, and we all know what that means.' So when I talked about saving money, it was taken pretty seriously."
But more important issues arose first. "When I came in, there was absolutely no clarity around the strategy at all," he says.
"When I asked my senior group, 'Where are we going?' I got four different answers. So then I reversed the order of what we
were going to do. Strategy came first, then we went after the overhead second."
Device Division One of the main concerns to emerge from those strategy sessions was the disparity between the company's business and its device
unit. "The pharma business was growing about 20 percent a year," Pyott explains. "And the device end of the business was growing
somewhere between zero and one percent. So it was like having a catamaran with two outboards-one churning out 20 knots and
one doing only one."
On closer examination, the executive team came to realize that everything about the two businesses was different. That included:
- gross margins-80 percent of sales for pharma, devices only 60 percent
- R&D-much more intense and expensive for pharma
- product lifecycle-seven to ten years for pharma; two to three for devices only
- product size-much larger for Rx sales.
So they decided to spin off the device business into an independent company that they have no stake in. "What I learned here
and at Novartis is that a well run pharma company will kill everything else in sight, " Pyott says. (See "David Pyott, Up
Close.")