Prevention of HIV-infection
This invention relates to the use of a parenteral formulation comprising the NNRTI TMC278 for the long term prevention of HIV infection in a subject at risk of being infected by HIV, which comprises the intermittent administration of the said formulation at long time intervals.
1. A method of maintaining a blood plasma level of 4-1000 ng/ml of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof in an individual at risk of being infected with HIV-1, comprising
subcutaneously or intramuscularly injecting a solution into the individual, intermittently at a time interval of at least one week, wherein said solution comprises:
sterile water;
a solubilizer or a surfactant; and
a dose, calculated on a basis of 0.2 mg/day to 50 mg/day of the time interval, of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof; or a pharmaceutically acceptable acid-addition salt thereof;
wherein the blood plasma level is maintained over the time interval.
2. The method according to claim 1 wherein the administration time interval is once every 3, 4, 6, 7, or 8 weeks.
3. The method according to claim 1 wherein the administration time interval is once every 1, 2, or 3 months.
4. The method according to claim 1 wherein the administration time interval is once every month.
5. The method according to claim 1 wherein the administration time interval is once every three months.
6. The method according to claim 1 wherein the blood plasma level of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof is maintained over the time interval at a level equal to or above 15 ng/ml.
7. The method according to claim 1 wherein the blood plasma level of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof is maintained over the time interval at a level equal to or above 20 ng/ml.
8. The method according to claim 1 wherein the blood plasma level of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof is maintained over the time interval at a level equal to or above 40 ng/ml.
9. The method according to claim 1 wherein the blood plasma level of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof is maintained over the time interval at a level below 40 ng/ml and above 4 ng/ml.
10. The method according to claim 1 wherein the solubilizer is a cyclodextrin or a cyclodextrin derivative or a polyethylene glycol.
11. The method according to claim 1 , wherein the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof; or a pharmaceutically acceptable acid-addition salt thereof is in base-form.
12. The method according to claim 1 wherein the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile occurs in its E-isomeric form.
13. The method according to claim 11 wherein the base form of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, occurs in its E-isomeric form.
14. The method according to claim 1 wherein the administration time interval is once every two months.
15. The method according to claim 3 wherein the time interval is 30 days and the dose of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof, ranges from 15 mg to 1,500 mg.
16. The method according to claim 3 wherein the time interval is 28 days and the dose of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof, ranges from 14 mg to 1,400 mg.
17. The method according to claim 1 wherein the dose is calculated on a basis of 1 mg/day to 10 mg/day.
18. The method according to claim 3 , wherein the time interval is 29 days and the dose of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof, ranges from 14.5 mg to 1,450 mg.
19. The method according to claim 3 , wherein the time interval is 31 days and the dose of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof, ranges from 15.5 mg to 1,550 mg.
20. The method according to claim 3 , wherein the time interval is about one month and the dose of the 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]-amino]benzonitrile, the E isomeric form thereof or the Z-isomeric form thereof, ranges from about 15 mg to about 1,500 mg.
21. The method according to claim 3 , wherein the dose is about 30 mg to about 300 mg.
22. The method according to claim 3 , wherein the dose is about 60 mg to about 150 mg.
23. The method according to claim 1 wherein the administration time interval is once every 4 weeks.
24. The method according to claim 1 wherein the administration time interval is once every 8 weeks.