Vaniqa In The News
Vaniqa for women has no major side effects
and may win FDA approval next year
Vaniqa:
Prescription Drug for Treating Facial Hair in Women
Dateline: 08/01/2000
Introduction: Vaniqa™ is a prescription drug which was recently
approved by the FDA in the United States for treating excessive
facial hair in women, which is often part of hirsutism.
It may be a welcome alternative for some of the estimated 20 million
American women for whom this problem is considered serious
enough to warrant tweezing, waxing, or shaving at least once a
week for hair removal. Vaniqa is actually not a brand
new drug, but rather a new topical-use version of the older drug
eflornithine (brand name Ornidyl). It was developed jointly
by Gillette and Bristol-Myers Squibb, and was approved on July
31, 2000. Ornidyl, the older drug, was approved in the U.S.
in 1990 and is used to treat tropical protozoal diseases and some
types of African sleeping sickness. Vaniqa, like Viagra,
is considered to be a "lifestyle drug", a drug which generally
improves our quality of life, but is not considered to be essential
for good health. It doesn't work for everybody, though.
Approximately 32% of the 393 patients treated with Vaniqa in the
pre-release clinical trials showed marked improvement, compared
to only 8% of the 201 control patients who used the vehicle (placebo)
alone.
Description: Technically speaking, Vaniqa is a cream
containing 13.9% (139 mg/g) of anhydrous eflornithine hydrochloride
as eflornithine hydrochloride monohydrate (150 mg/g).
Indications
and Usage: Vaniqa
(eflornithine hydrochloride) cream is indicated for the reduction
of unwanted facial hair in women.
Vaniqa has only been studied on the face and adjacent involved
areas under the chin, and usage should be limited to those areas.
How
Vaniqa Works: Vaniqa probably works by inhibiting
an enzyme in human skin that stimulates hair growth. It
is not a hair remover or depilatory, but most likely decreases
hair growth and exerts antitumor effects and antiprotozoal effects
by the same mechanism. Specifically, Vaniqa causes irreversible
inhibition of the enzyme ornithine decarboxylase, which is necessary
for cell growth and division in mammals. Rapidly dividing
cells, such as hair cells, appear to be most susceptible to the
effects of the drug.
Effectiveness: Approximately 32% of the 393 female
patients treated with Vaniqa in the clinical trials showed marked
improvement (reduction of unwanted facial hair), compared to only
8% of the 201 control patients who used the vehicle (placebo)
alone. These results are based on the pre-release clinical
trials, in which Vaniqa was used twice daily for 24 weeks.
Improvement was often seen in as few as four to eight weeks of
treatment. After discontinuing Vaniqa treatment, facial
hair growth approached pre-treatment levels within eight weeks.
Safety
and Side Effects:
Observed side effects of Vaniqa in the clinical trials were relatively
mild. They included temporary redness, stinging, burning,
tingling, rash, "razor bumps," and acne. These side effects
were observed in the clinical studies, which used a relatively
small number of women, and it's unlikely that very rare side effects
would have been detected in those studies. More serious
side effects, similar to those which occur when the drug is used
for African sleeping sickness, would be expected if the drug were
ingested orally, or used excessively (multiple tubes per day)
on non-facial areas of the body. Vaniqa is classified as
"pregnancy category C", which, in this case, means that animal
studies have shown that it has an adverse effect on the fetus
but there are no adequate studies in humans. For practical
purposes, that means to avoid the drug during pregnancy unless
it's absolutely necessary.
Conclusions: Although unwanted facial hair in women
is not a serious illness, it is often part of hirsutism and can
be very disconcerting to those women who have it. Vaniqa
is the first prescription drug approved in the United States to
treat this condition. It was effective, compared to placebo,
in approximately 25% of women who used it during the pre-release
clinical trials. Although Vaniqa currently appears have
few side effects, when used as directed, post-release experience
often modifies the safety profile for new drugs. Potential
risks of using a new drug should be carefully compared to the
benefits to be derived before using this drug for it's effect
on excessive facial hair.
References:
·
Drugs for Parasitic Infections,
Med Lett Drugs Ther, 1993, 35(911):111-22.
·
Vaniqa Prescribing Information
From the FDA. Requires the Adobe Acrobat Reader (free download).
·
Monographs on "eflornithine"
from Clinical Pharmacology 2000 and The Worldwide Drug Database.
Access to each is free, but requires an extensive registration
procedure.
Vaniqa Approved As Treatment For Women With Unwanted Facial
Hair -Bristol-Myers
Squibb- 07/31/2000
Press
Release:
Princeton, New Jersey, July 31, 2000 - Bristol-Myers Squibb Company
(NYSE:BMY) and The Gillette Company (NYSE:G) announced today that
the U.S. Food and Drug Administration (FDA) has approved Vaniqa™ (eflornithine hydrochloride)
Cream, 13.9% as the first topical prescription treatment for women
with unwanted facial hair. Vaniqa works by inhibiting the
growth of facial hair, and was shown in controlled clinical trials
to provide clinically meaningful and statistically significant
improvement in the reduction of facial hair growth in women.
The
FDA approval of Vaniqa may provide an important
new option for the more than 41 million women in the United States
with unwanted facial hair. Unwanted facial hair can affect women
of all ages, races and ethnic backgrounds. The impact of this
surprisingly common problem extends beyond the need for regular
tweezing, waxing or depilatory application. Many women who have
unwanted facial hair often report that the condition negatively
impacts their lifestyle and makes them feel unfeminine and less
confident.
“As
a physician, I am excited about the potential for this new prescription
cream to help women manage unwanted facial hair,” said Marty E.
Sawaya, M.D., PhD, adjunct professor, Department of Biochemistry
and Molecular Biology, University of Miami, and a dermatologist
and clinical research investigator at ARATEC Clinics in Ocala,
Florida. “Importantly, Vaniqa will potentially help
millions of women with this condition to feel less bothered by
their facial hair and the amount of time they spend removing,
treating or concealing it.”
Vaniqa
(eflornithine hydrochloride) Cream, 13.9% was developed through
a unique partnership between The Gillette Company and Bristol-Myers
Squibb. The companies formed the partnership in 1996 in order
to complete development of the product. Bristol-Myers Squibb is
responsible for worldwide clinical development, regulatory submissions
and, together with Gillette, is responsible for marketing this
prescription product.
“Bristol-Myers
Squibb is pleased that the FDA has approved Vaniqa as the first lifestyle
prescription drug available to treat unwanted facial hair,” said
Richard J. Lane, president, Worldwide Medicines Group, Bristol-Myers
Squibb. “As a result of our partnership with The Gillette Company,
we can now provide physicians with an effective way to help their
patients who are affected by this problem.”
In
most cases, unwanted facial hair is caused by hereditary factors.
A small number of cases are caused by medical conditions such
as androgen excess disorder or polycystic ovarian syndrome. Regardless
of the cause, Vaniqa (eflornithine hydrochloride)
Cream, 13.9% demonstrated in clinical trials that it is effective
in slowing the growth of unwanted facial hair in up to 60 percent
of women. Vaniqa
takes up to 2 months to work, and along with Vaniqa, women should continue
to use their current method of hair removal.
Vaniqa
has a unique mechanism of action and is believed to work by blocking
an enzyme that is necessary for hair growth. In Phase III clinical
trials, the primary study measure was a physician’s global assessment
of their patients’ improvement at the end of 24 weeks. Results
demonstrated clinically and statistically significant improvement
in the reduction of facial hair growth in women treated with Vaniqa as compared to the group
that was treated with vehicle (a placebo cream). Significant differences
between Vaniqa
and vehicle were seen as soon as eight weeks into treatment. The
data from the Phase III clinical studies show that among those
who completed 24 weeks of treatment, nearly 60 percent of patients
on Vaniqa improved.
In
clinical trials, when side effects occurred they were mild and
generally resolved without treatment. The most common side effects
associated with Vaniqa were minor skin irritations
such as temporary redness, hair bumps, stinging, burning, tingling,
acne, or rash.
“Until
now, no prescription creams have been available that help slow
the rate of unwanted hair growth,” said Mary Ann Pesce, vice president,
New Products, The Gillette Company. “This unique partnership with
Bristol-Myers Squibb reflects the ongoing commitment of The Gillette
Company to develop products specifically designed to meet the
grooming and beauty needs of women.”
Women
who are interested can learn more about Vaniqa
by consulting with their physician or by calling 1-877-829-9715.
Vaniqa will be available in pharmacies
as early as September.
SOURCE: Bristol-Myers Squibb
FDA Approves Facial Hair Treatment -Tracee Cornforth-
© 2000 About.com
The
FDA has approved an important new treatment option for the more
than 41 million women in the United States with unwanted facial
hair. Unwanted facial hair affects women of all ages, races, and
ethnic backgrounds.
The
problem of unwanted facial hair extends beyond the normal need
for tweezing, waxing, or depilatory application. Many women with
excess facial hair suffer negative impact on their lifestyle that
often makes them feel unfeminine and less confident.
The
Bristol-Myers Squibb Company and The Gillette Company announced
the FDA approval of Vaniqa™ (eflornithine hydrochloride) Cream,
13.9% as the first topical prescription treatment for women with
unwanted facial hair. Vaniqa works by inhibiting the growth of
facial hair. In controlled clinical trails, the drug was shown
to clinically meaningful and statistically significant improvement
in the reduction of facial hair growth in women.
"As
a physician, I am excited about the potential for this new prescription
cream to help women manage unwanted facial hair," said Marty E.
Sawaya, M.D., Ph.D., adjunct professor, department of biochemistry
and molecular biology, University of Miami, and a dermatologist
and clinical research investigator at ARATEC Clinics in Ocala,
Florida. "Importantly, Vaniqa will potentially help millions of
women with this condition to feel less bothered by their facial
hair and the amount of time they spend removing, treating, or
concealing it."
A
unique partnership, formed in 1996, between The Gillette Company
and Bristol-Myers Squibb led to the development of Vaniqa Cream,
13.9%. Bristol-Myers Squibb is responsible for worldwide clinical
development, regulatory submissions and, together with Gillette,
is responsible for marketing this prescription product.
"Bristol-Myers
Squibb is pleased that the FDA has approved Vaniqa as the first
lifestyle prescription drug available to treat unwanted facial
hair," said Richard J. Lane, president, Worldwide Medicines Group,
Bristol-Myers Squibb. "As a result of our partnership with The
Gillette Company, we can now provide physicians with an effective
way to help their patients who are affected by this problem."
Hereditary factors
are usually the cause of unwanted facial hair in women; however
a small number of cases are caused by medical conditions such
as androgen excess or polycystic ovary syndrome. Vaniqa Cream
13.9% demonstrated in clinical trials that it is effective in
slowing the growth of unwanted facial hair in up to 60 percent
of women without regard to cause.
Vaniqa
can take up to 2 months to work, and women should continue to
use their current hair removal method until the drug is working
effectively. Vaniqa has a unique mechanism of action and is believed
to work by blocking an enzyme that is necessary for hair growth.
After
24 weeks, patients in Phase III clinical trials, saw significant
improvement in the reduction of facial hair growth in women treated
with Vaniqa as compared to the group that was treated with vehicle
(a placebo cream). Significant differences between Vaniqa and
vehicle were seen as soon as eight weeks into treatment. The data
from the Phase III clinical studies show that among those who
completed 24 weeks of treatment, nearly 60 percent of patients
on Vaniqa improved.
Side
effects were mild and usually resolved without treatment. Minor
skin irritations such as temporary redness, hair bumps, stinging,
burning, tingling, acne, or rash were the most common side effects
associated with Vaniqa.
Vaniqa
is the first prescription cream available to help slow the rate
of unwanted hair growth. Women can learn more about Vaniqa by
consulting their physicians or by calling 1-877-829-9715. Vaniqa
is expected to be available in pharmacies in September.
New cream stops facial hair on women
NEW
YORK (AP) - They pluck, they bleach, they tweeze. They use hot
wax, electric current and lasers. Some even shave daily. And still
the hair comes back.
About
one in six American women has enough facial hair that they remove
it at least once a week.
Now,
Gillette Co., the world's biggest manufacturer of razors, and
pharmaceutical maker Bristol-Myers Squibb Co. have developed the
first prescription cream that stops the growth of facial hair
in women.
The
drug could win Food and Drug Administration approval as early
as next year.
Vaniqa
(pronounced van-ih-KAH) is applied to the face like a moisturizer
twice a day. It works by blocking the enzyme that makes hair grow.
It must be used regularly or hair growth will resume. Studies
show it helps most women and has no major side effects.
Vaniqa
appears to work in men as well - but the makers are trying to
prove themselves with women first.
Facial
hair in women has several causes, including an excess of male
hormones. Genetics can also play a role. For instance, women of
Mediterranean or Hispanic descent tend to have more facial hair.
The
condition, known medically as hirsutism, can damage a woman's
self-esteem. ''It's very destructive, psychologically,'' said
Dr. Ricardo Azziz, professor of obstetrics and gynecology at the
University of Alabama-Birmingham.
Azziz
said current treatments are only moderately successful, and Vaniqa
may be preferable because creams cause fewer side effects.
No
one has to convince Ingrid Reyes, 29, a chemist from New York
City. Reyes said she has had sideburns and dark hair above her
lip since she was a teen-ager.
''I've
been on a date and suddenly he notices it and says, 'You have
a lot of hair.' He doesn't mean any harm, but it makes you feel
uncomfortable,'' she said.
Reyes
tried waxing to remove the hair. But that dried out her skin.
She tried plucking it. But the hair only grew back thicker.
Lately
she has been receiving electrolysis, which gets rid of hair permanently
by delivering electrical current through a needle placed into
the hair follicle. But multiple treatments are required and -
at $75 each - they are stretching her budget.
Other
methods also have shortcomings. Shaving causes stubble and skin
may become irritated. Depilatories, or creams that remove hair,
can irritate the skin.
Some
physicians have prescribed birth control pills, but many women
don't want to take them because they can cause weight gain and
other side effects. Physicians recently started using lasers to
kill hair follicles but that is also expensive, and can cause
scarring.
''It
will be nice to give women something they do not have to take
by mouth, and it's certainly less painful than electrolysis,''
said Dr. Ken Washenik, a dermatologist at New York University
who helped study the drug. The only side effect was a rash on
some women, he said.
The
companies have not set a price yet for Vaniqa. Like other ''lifestyle''
drugs such as those that fight baldness, the cream probably won't
be covered by insurance.