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Vaniqa Cream News
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Vaniqa
In The News
Vaniqa for women has no major side effects
and permanently removes unwanted facial hair.
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.
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.
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