PRESS
RELEASES
January
22, 2007
“Dermatologist discovers “Oral
Nickel” cures most common jewelry allergies”
"Psorizide® Forte, an oral tablet used to treat metal/jewelry
allergy, provides new tool for Dermatologists and Allergists"
Click
here to download release-specific image, then right click
on image and “Save Picture As”
(for journalistic use only)
December
18, 2006
“Plymouth Pharmaceuticals® launches
new drug, Eczemol®, for Pediatricians, Dermatologists, and Family
Practitioners”
"Eczemol®, a novel, oral medication for treating eczema/atopic
dermatitis"
December
11, 2006
“Plymouth Pharmaceuticals® and Dermatologist
launch new oral prescription acne medication (Acunol™)”
"Acunol™, a new medication for treating acne and rosacea, is
born."
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COMPANY
FACTS
Plymouth Pharmaceuticals™ was incorporated in 1991 under the
direction of Steven A. Smith, M.D., FACP, a dermatologist; his original
intent was to create a new treatment for people who suffer with
psoriasis. Dr. Smith originally initiated a traditional, allopathic
IND (Investigational New Drug) application process with FDA (Food
& Drug Administration) to get his ORAL psoriasis medication
approved for use in the United States. The term “allopathic
(conventional) medicine” was coined in 1842 by Dr. Samuel
Hahnemann, the father of homeopathy, and has been used ever since
to distinguish “homeopathic” medicines from traditional
medicines (those having gained FDA approval through an IND application).
Two
years after filing the IND application, Dr. Smith discovered that
the main components of his psoriasis medication were already “grandfathered
in” under the HPUS (Homeopathic Pharmacopoeia of the United
States). The USP (United States Pharmacopoeia) is used for all allopathic
medicines and dietary supplements worldwide. All ingredients, including
those Dr. Smith had discovered, listed in the HPUS were already
accepted by FDA as safe; therefore, Loma Lux® Psoriasis could
be marketed by filing only a handful of forms with FDA. Loma Lux’s
only cost would be to ramp up inventory and market the product.
This allowed the company to leapfrog many of its competitors without
the need for a typical IND process, which is can take up to 15 years
and $300 million just to get a new drug approved by FDA.
The
launch of a homeopathic OTC (over the counter) psoriasis product
as well as others for other diseases (acne, eczema, asthma, and
sinus/allergy) came in 1996; these products were and still are sold
under the Loma Lux® brand. The Loma Lux® AcnePill™
has nationwide distribution in the Target chain of stores. Most
of the Loma Lux® products are also sold through various online
distributors, among them www.amazon.com
and www.drugstore.com.
In 1999, the company launched its first homeopathic “Rx only”
product, Psorizide® Ultra, to treat psoriasis, eczema, and seborrhea.
Psorizide® Ultra was then reformulated for the treatment of
psoriasis specifically and became Psorizide® Forte (Rx) in 2001;
at that time Psorizide® Ultra’s indication became solely
the treatment of eczema and seborrhea. Eczemol® (Rx) for the
treatment of moderate to severe eczema, and Acunol™ (Rx),
for the treatment of mild to moderate acne were launched in 2006.
All prescription products are sold under the Plymouth Pharmaceuticals™
brand.
Pharmaceutical Products:
Loma Lux® Consumer Health Care Products:
For
more information, visit http://www.lomalux.com
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