Medicaments comprising relaxin and their use

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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C514S880000

Reexamination Certificate

active

06395706

ABSTRACT:

FIELD AND BACKGROUND OF THE INVENTION
The present invention relates to use of relaxin in the manufacture of medicaments having a novel application, to a method in which relaxin is utilized for the treatment and prevention of certain conditions and to pharmaceutical compositions comprising relaxin.
Relaxin otherwise known as Cervilaxin, and formerly referred to as Releasin, is a polypeptide hormone secreted by the
corpora lutea
of many mammalian species during pregnancy.
As described e.g. in U.S. Pat. No. 3,096,246, the contents of which are incorporated herein by reference, relaxin is present in the ovaries of animals and may be extracted therefrom. It is believed to be a hormone of pregnancy and has aroused great interest in the field of medical research. For instance, it has been known to cause uterine cervix relaxation in cows; to increase the dilatability of the uterine cervix in ovariectomized estrogen-primed hogs; to cause definite milk let-down in sheep, and, to a lesser extent, in cows, and to cause marked lobulo-alveolar growth of the mammary gland in rats; and, in the clinic, it has been found to cause dilation of the uterine cervix in near-term pregnant women who fail to dilate after injections of pitocin, and to stop premature labor in certain female patients, allowing them to go to term.
EP 08664g, the contents of which are incorporated herein by reference, relates to the molecular cloning and characterization of the gene sequence coding for porcine relaxin. Thus, recombinant DNA techniques for the preparation of porcine relaxin were described more than ten years ago. However, before the advent of the present invention application of relaxin has been restricted essentially to pregnancy- and gynecologically-related uses.
SUMMARY OF THE INVENTION
It has now been found in accordance with the present invention that relaxin can be used to treat and prevent cutaneous aging, androgenetic alopecia and related conditions, and thus to encourage hair growth and to prevent hair loss.
Thus in one aspect, the invention provides use of relaxin in the manufacture of a medicament for the treatment and prevention of a condition selected from cutaneous aging, androgenetic alopecia and related conditions, e.g., atrophy, sclerosis and miniaturization of the hair and hair follicles. The medicament may comprise relaxin in combination with a pharmaceutically acceptable, e.g. topically acceptable, carrier, and may be used, for example, for prolonging the duration of the anagen stage of hair growth.
In another aspect, the invention provides a method for the treatment and prevention of a condition selected from cutaneous aging, androgenetic alopecia and related conditions, which comprises administering to a human in which said treatment or prevention is desired, an effective amount of relaxin. In this method, relaxin may be administered in combination with a pharmaceutically acceptable (e.g. a topically acceptable) carrier. The method may thus be used, e.g. , for the treatment and prevention of a condition selected from atrophy, sclerosis and miniaturization of the hair and hair follicles, or for prolonging the duration of the anagen stage of hair growth.
In yet another aspect, the invention provides a pharmaceutical composition for the treatment and prevention of a condition selected from cutaneous aging, androgenetic alopecia and related conditions, which comprises relaxin in combination with a pharmaceutically acceptable carrier, e.g. a topically acceptable carrier.
DETAILED DESCRIPTION OF THE INVENTION
As is known, the cyclic activity of the hair is divided into three stages: a period of active growth known as anagen, a short transition phase called catagen, and a resting period which ends in hair loss, called telogen.
It is also an accepted fact that the percentage of follicles in anagen rises steeply during pregnancy, when as many as 95% of the follicles are active. Two to four months after parturition, the proportion falls to less than 70%. Thus it appears that the hormonal conditions of late pregnancy prolong anagen, and follicles are consequently precipitated into telogen via catagen after parturition.
Androgenetic alopecia (AA) , which is also called common baldness, or male pattern baldness, independent of its causes, is the cutaneous aging of a particular zone, the scalp. AA can be defined, on one hand, as atrophy, sclerosis or miniaturization of the hair follicle, and on the other hand, a progressive shortening of the average duration of the anagen stage, which results in vellus hair prior to complete disappearance.
The dermal papilla is a connective tissue structure situated at the base of the hair follicle. In anagen follicles, the papilla invaginates the epithelial hair bulb matrix, remaining in contact with the fibrous sheath surrounding the follicle via a narrow stalk at its base.
The papilla is composed of specialized fibroblast-like cells and the root sheath contains fibroblast population. The dermal papilla plays a fundamental role in induction, maintenance and regulation of hair growth.
During anagen, the papilla cells lie in an extracellular matrix rich in mucopolysaccharides and basement membrane proteins and display ultra-structural features indicative of synthetic activity. The extracellular matrix gradually diminishes during catagen and disappears almost completely during telogen. It is now generally accepted that fibroblasts are responsible for the manufacture of all the dermal connective tissue elements or their precursors, i.e., ground substance, collagen and elastin.
Relaxin influences the fibroblasts and fibroblast-like cells of the pilosebaceous unit. Relaxin treatment, either topically or systematically, will result in preventing atrophy, sclerosis and miniaturization of the hair, by prolonging the duration of the anagen stage, or otherwise. It will remodulate the aging process in general and in particular the AA in male and female.
Thus, according to the present invention, there is provided a composition which can be applied topically in lotion, gel or cream form, or systematically for internal or parenteral use, in the form of capsules, tablets or ampules, for treatment of androgenetic alopecia and related conditions such as alopecia areata, anagen effluvium, telogen post-partum alopecia, diffuse alopecia, and alopecia androgenica.
Similarly, the composition of the present invention could be used in the prevention and treatment of cutaneous aging in areas other than the scalp.
Said compositions can be in the form of creams, lotions, ointments or gels, prepared for use in any conventional manner, in admixture with one or more physiologically acceptable carriers and diluents.
The compositions may take such forms as suspension, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as emulsifying, suspending, stabilizing, gelling and/or dispersing agents.
Alternatively, the active ingredients may be in powder form for constitution with a suitable vehicle, e.g., sterile, pyrogen-free water, free water, before use.
While it is possible for the active ingredients to be administered alone, it is preferable to present them as pharmaceutical formulations. The formulations of the present invention comprise at least one active ingredient, as above defined, together with one or more acceptable carriers therefor and optionally other therapeutic ingredients. The carrier(s) must be acceptable in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
The formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. Such methods include the step of bringing into association the active ingredient with the carrier, which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers, or both, and then, if necessary, shaping the product.
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