Antiviral pharmaceutical for topical administration

Abstract

An enzymatically-active ribonuclease is combined with a vehicle that does not unacceptably interfere with such enzymatic activity and applied externally. Advantageously, the ribonuclease is ranpirnase. The vehicle can be a liquid, a gel, an ointment, or a serum, and can also be an approved sexual lubricant.

Claims

1. A topical pharmaceutical composition consisting essentially of a therapeutically effective amount of an enzymatically-active ribonuclease and a viscous vehicle that does not unacceptably interfere with the enzymatic activity, wherein the vehicle is selected from the group consisting of a gel, a serum, or a lotion.

2. The pharmaceutical composition of claim 1, wherein the enzymatically-active ribonuclease is ranpirnase.

3. The pharmaceutical composition of claim 2, wherein the pharmaceutical contains between 1 and 3 mg of ranpirnase per ml of vehicle.

4. The pharmaceutical composition of claim 2, wherein the concentration of ranpirnase in the pharmaceutical composition is chosen to deliver between 1 and 3 mg of ranpirnase to the patient each week that the pharmaceutical composition is administered to the patient in accordance with the dosage regimen used.

5. The pharmaceutical composition of claim 1, wherein the vehicle is compatible with latex condoms.

6. The pharmaceutical composition of claim 1, wherein the vehicle is an aqueous vehicle.

7. The pharmaceutical composition of claim 6, wherein the vehicle is an approved sexual lubricant.

Description

BRIEF DESCRIPTION OF THE DRAWING

(1) FIG. 1 shows the global performance of evaluable patients treated with the invention in a Phase I study;

(2) FIG. 2 shows the number of patients who achieved clinical healing at weeks 4 and 8 in the Phase I study; and

(3) FIG. 3 shows the time required for patients in the Phase I study to reach clinical healing.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

(4) A Phase I compassionate use clinical study was conducted in Buenos Aires. Male volunteers who were diagnosed with anogenital warts in various locations (scrotum, penis shaft, penis dorsum, inguinal, perianal) were accrued to the study. The study had three arms. In arm A, the tested embodiment was ranpirnase combined with a vehicle supplied by JRX Biotechnology, Inc. (In this instance, the ranpirnase was reconstituted from lyophilized powder.) In arm C, the tested embodiment was also ranpirnase combined with the same JRX Biotechnology, Inc. vehicle, but in this instance the ranpirnase had been previously frozen and was thawed prior to use. These two combinations were very low-viscosity liquids; each was applied topically twice each day. The vehicle used in these two arms is a polysaccharide megasphere formulation; on information and belief it is covered by U.S. Pat. Nos. 6,759,056, 6,946,144, 7,201,919, 7,220,427, 7,300,666, and 7,316,820. In arm B, the tested embodiment was ranpirnase combined with K-Y Brand Jelly. This second embodiment was formulated from ranpirnase reconstituted from lyophilized powder; it is a viscous gel that was applied topically three times each day. In each arm, the concentration of ranpirnase was 1 mg ranpirnase to 1 ml of vehicle.

(5) As can be seen in FIG. 1, 22.6% of all the patients in the study achieved clinical healing by the 4th week of treatment, with 61.3% of all the patients having reached a 50% improvement by that time. FIG. 1 also shows that 95.2% of all the patients achieved clinical healing by the 8.sup.th week, with 4.7% of all the patients having reached a 50% improvement in this time. Although the long-term effect of this treatment is not yet known, this short-term effect is far better than has been reported for other pharmaceuticals (Podofilox solution and gel, Aldara Cream, Veregen ointment).

(6) FIG. 2 graphically displays the information in the three leftmost columns in FIG. 1. To a person of ordinary skill in this art, FIG. 2 is strong evidence that the invention is reasonably correlated with usefulness in treating HPV. FIG. 2 shows that 100% of the evaluable patients in arms A and C achieved clinical healing by the 8.sup.th week, and 83.3% of the patients in arm B achieved clinical healing by that time. Overall, 95.2% of all patients achieved clinical healing by the 8.sup.th week.

(7) FIG. 3 displays the average time required for patients in each of the three arms, and in the study as a whole, to reach clinical healing. The patients in arm B required more than 40 days to reach clinical healing, while the patients in arms A and C reached clinical healing sooner (in approximately 32 and 34 days, respectively).

(8) Although these results may seem to indicate that the second preferred embodiment used in arm B of the study is not as active against HPV as the first preferred embodiment used in arms A and C, the study did not include enough patients to permit such a conclusion to be drawn.

(9) This study did not address the question of dosage; in all arms of the study the quantity of ranpirnase delivered to the patient was 1 mg/week. The activity of the preferred embodiment may be improved by increasing the concentration of ranpirnase from 1 mg/ml to 3 mg/ml, whereby the weekly dose of ranpirnase administered to each patient would be increased to 3 mg, but this has not yet been tested.

(10) It will be understood that although the invention has been developed for use in treatment of anogenital warts, its use is not restricted to this application. The invention may have other antiviral applications. Although the invention is presently applied to external anogenital warts, it may also be useful when applied vaginally, extra-vaginally, intra-vaginally, anally, peri-anally, and intra-anally. Although the preferred embodiment uses ranpirnase as the enzymatically-active ribonuclease, other ribonucleases having similar enzymatic activities exist and may be used instead. Furthermore, while treatment of anogenital warts may be easier using a viscous vehicle such as a gel because it is easier to apply a gel to an anogenital wart and a gel is less likely to run off and is therefore more likely to remain where it has been applied, there may be other applications in which a liquid vehicle, or an ointment vehicle will be preferable. The vehicle may alternatively be a serum, a lotion, or an approved sexual lubricant, i.e. a lubricant that meets applicable governmental requirements and is intended for use on human genitalia.

(11) Although at least one preferred embodiment of the invention has been described above, this description is not limiting and is only exemplary. The scope of the invention is defined only by the claims, which follow: