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Interview
with BioPhysica on
Eucapil®
(fluridil) - "A Novel Topical Antiandrogen"
According to Dermatologic Surgery |

Diagram
taken
from Eucapil's instructions sheet
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The following is
provided by
courtesy of Frizz in the Topical Forum
DISCLAIMER
Interpharma Praha, a.s., the manufacturer of fluridil and
Eucapil ® , and
Biophysica, Inc., the holder of patent rights to fluridil, are not
responsible for the
correctness, completeness, reliability or usefulness of the
information provided
below. Viewing these questions does not constitute a consultation or
the
rendering of advice. While there may be information below related to
certain
medical conditions and their treatment, should a medical condition
exist, promptly
see your own physician or health care provider. Please consult the
labeling of
this cosmetic product before using
it.
Is Eucapil still effective if people shampoo their hair daily? Is it
absolutely
necessary that the user shampoos
no more than once or twice a week?
First, one would generally assume
that applying any medium on the scalp and
then washing it away would probably be counter-productive. Second,
Eucapil
was designed to degrade in the water environment. This is a security
feature. We
do know that fluridil is reabsorbed by the skin only and there is no
evidence for
reabsorption and systemic effects: still, should Eucapil for
whatever reason enter
the circulation, it would decompose. Therefore, it is important not
to apply fluridil
to the scalp when wet. Third, shampoos remove the skin and hair fat
and thus
signal to the sebaceous glands to work harder: a vicious circle is
thus
established. We hear from Eucapil users who have reduced their
shampooing
frequency, washed hair with warm water only, or used the so-called
"dry
shampoos" that although it took many weeks before the scalp
glands returned to
normal, they eventually did. Some users report that washing their
hair in the
morning and applying Eucapil at night
works for them.
Since fluridil is already available and used in the Czech and Slovak
Republics,
what are the definitive clinical published results? Are people
reporting it as the
best cure for MPB? Does it work better on certain people with
certain types of
hair loss?
For clinical data, please refer to
the article published in Dermatologic Surgery
(Sovak et al., Fluridil, a rationally designed topical agent for
androgenetic
alopecia: first clinical experience. Dermatol Surg 28:678-685, 2002,
with an
erratum on p. 972). In addition, a summary of the entire 12-month
trial is included
in a paper published in Drug Development Research (Seligson et al.,
Development of fluridil, a topical suppressor of the androgen
receptor in
androgenetic alopecia, Drug Dev Res 59:292-306, 2003). From the
post-marketing
data’s preliminary feedback and the ongoing studies it appears
that
Eucapil is effective in patients with androgenetic alopecia, in that
its best effect is
seen – already after a few weeks of use – in substantially
reducing or stopping
hair loss, and upon longer use, increasing the average hair
diameter, which gives
the impression of greater hair fullness. The best results seem to be
achieved in
those subjects who have not yet established long-term alopecia and
who have
viable hair follicles. Thus, there will always be individually
different
responsiveness to deal with.
What is the topical/local half-life before Eucapil is
absorbed/distributed into the
circulation?
Fluridil was designed not to be
resorbed beyond the scalp skin. Only traces of
decomposed Eucapil were found in the circulation of some subjects
who used
the product over extended periods of time. Fluridil is also designed
to degrade in
an aqueous environment in order to prevent systemic side effects.
The topical
half-life cannot be determined as it depends on the individual
humidity and
overall condition of the skin.
How soon can we expect the release of Eucapil in France and other
European
countries?
The substance fluridil has been
approved in France, and approval of Eucapil
(2% solution in rubbing alcohol) is still pending. Fluridil has also
been submitted
for approval in other EU countries, however, it is difficult to
predict the timing of
the regulatory agencies.
Can patients use minoxidil or perhaps other water based topicals in
combination with Eucapil? If people can use minoxidil in combination
with fluridil,
do they apply minoxidil before,
after or simultaneously with fluridil?
We have not studied the
combination of Eucapil and minoxidil for treatment of
androgenetic alopecia in a clinical setting, but plan to do so in
the future since we
have heard laudatory comments from the market. If users of fluridil
decide to
explore the combination, it would be reasonable – for the reasons
of stability
stated above – that minoxidil be applied first and then Eucapil
after, when the
scalp is completely dry, surely not at the same time. The current
formulation of
minoxidil contains water, which can
cause the decomposition of fluridil.
Are there plans to release higher concentrations of fluridil since
Eucapil only
contains 2% fluridil? Is fluridil
dose dependent?
We have seen no reason for that.
How would you compare the effectiveness of Eucapil to that of
finasteride,
dutasteride and minoxidil,
respectively?
Eucapil has not yet been tested in
a head-to-head clinical study with the
therapies you refer to. The data in the two articles from
Dermatologic Surgery
and Drug Development Research (referred to above) can be compared to
published data for these and other
products.
Are there plans to release Eucapil as a cosmetic treatment first in
the U.S.
before your company proceeds to
apply for FDA approval?
No. Eucapil, albeit a cosmetic
agent, would be (under the current regulations)
considered to be a drug by the U.S.
FDA.
In Table 4 of the
article in Dermatologic Surgery (referenced above), why is it
that Eucapil did no more than placebo on the anagen ratio but had
such obvious
photographic effects after three
months that the placebo arm was abandoned?
Please revisit Table 4 and the
text of the article. Eucapil did produce a
statistically significant increase in anagen and decrease in telogen
counts after
three months when compared to placebo. The placebo arm of the study
was
terminated (i.e., placebo patients received Eucapil) according to
the study
protocol because the anagen/telogen ratios improved in more than 40%
of the
Eucapil group subjects after three months. It would, therefore, not
have been
ethical to continue the placebo treatment. In addition, it has been
found that
Eucapil in a number of subjects increased the average hair diameter,
giving the
impression of "fullness" of the hair, even though the
absolute number of hairs has
not changed dramatically.
Related information
Fluridil,
a Rationally Designed Topical Agent for Androgenetic Alopecia: First
Clinical Experience (pdf file)
Fluridil
instructions (courtesy of Col in Topical Forum) (pdf file)
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Information
about this article |
| Article # |
274 |
| Title |
Q&A
with BioPhysica on Eucapil (fluridil) |
| Date |
09/10/03 |
| Source |
Frizz
(topical forum) |
| Forum |
Topical
Forum |
| Archive |
Topicals |
| Contact |
hairsite@aol.com |
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