Method of reducing pulmonary exacerbations in respiratory disease patients
Described are methods of reducing pulmonary exacerbations and methods of treating cystic fibrosis, including methods of reducing pulmonary inflammation, comprising administration of an LTA4h inhibitor.
1. A method of reducing pulmonary exacerbations in a cystic fibrosis patient, wherein the patient is undergoing concomitant treatment with a CFTR modulator and wherein the patient has an FEV 1 pp greater than or equal to about 68% at baseline, the method comprising orally administering to the patient acebilustat at a total daily dose of about 100 mg or less, and wherein the CFTR modulator is selected from the group consisting of ivacaftor, lumacaftor, tezacaftor, VX-445, VX-659, VX-440 and VX-152, or a combination of any of thereof.
2. The method of claim 1 , wherein acebilustat is administered at a total daily dose of about 100 mg.
3. The method of claim 2 , wherein acebilustat is administered at a total daily dose of about 50 mg.
4. The method of claim 1 , wherein the CFTR modulator is ivacaftor.
5. The method of claim 1 , wherein the CFTR modulator is lumacaftor or tezacaftor.
6. The method of claim 1 , wherein the patient has an FEV 1 pp greater than or equal to about 70% at baseline.
7. The method of claim 1 , wherein the patient has an FEV 1 pp greater than or equal to about 75% at baseline.
8. The method of claim 1 , wherein the patient experiences a decrease in the rate, number, or frequency of pulmonary exacerbations in the twelve month period after initiating treatment with acebilustat.
9. The method of claim 1 , wherein the patient does not experience a pulmonary exacerbation for at least forty-eight weeks after initiating treatment with acebilustat.
10. The method of claim 1 , wherein the patient experiences a decreased number of pulmonary exacerbations in the twelve month period after initiating treatment with acebilustat as compared to the number of pulmonary exacerbations in the twelve month period prior to initiating treatment with acebilustat.
11. The method of claim 1 , wherein the CFTR modulator is ivacaftor or a-combination drug comprising ivacaftor.
12. The method of claim 11 , wherein the combination drug is lumacaftor/ivacaftor.
13. The method of claim 11 , wherein the combination drug is a triple combination.
14. The method of claim 13 , wherein the triple combination comprises ivacaftor, tezacaftor, and one of VX-445, VX-659, VX-440 and VX-152.
15. The method of claim 1 , wherein the CFTR modulator is a combination of any of ivacaftor, lumacaftor, tezacaftor, VX-445, VX-659, VX-440 and VX-152.
16. A method of reducing pulmonary exacerbations in a cystic fibrosis patient, wherein the patient is undergoing concomitant treatment with a CFTR modulator, the method comprising measuring FEV 1 pp in the patient at baseline, and orally administering acebilustat at a total daily dose of about 100 mg or less to the patient if the patient has an FEV1pp greater than or equal to about 68% at baseline;
wherein the CFTR modulator is selected from the group consisting of ivacaftor, lumacaftor, tezacaftor, VX-445, VX-659, VX-440 and VX-152, or a combination of any of thereof.
17. The method of claim 16 , wherein the patient has an FEV1pp greater than or equal to about 70% at baseline.
18. The method of claim 16 , wherein the patient has an FEV1pp greater than or equal to about 75% at baseline.
19. The method of claim 16 , wherein the CFTR modulator is a combination of any of ivacaftor, lumacaftor, tezacaftor, VX-445, VX-659, VX-440 and VX-152.
20. The method of claim 19 , wherein the combination drug is lumacaftor/ivacaftor.
21. The method of claim 19 , wherein the combination drug is a triple combination.
22. The method of claim 21 , wherein the triple combination comprises ivacaftor, tezacaftor, and one of VX-445, VX-659, VX-440 and VX-152.
23. The method of claim 16 , wherein the patient experiences a decrease in the rate, number, or frequency of pulmonary exacerbations in the twelve month period after initiating treatment with acebilustat.
24. The method of claim 16 , wherein the patient experiences a decreased number of pulmonary exacerbations in the twelve month period after initiating treatment with acebilustat as compared to the number of pulmonary exacerbations in the twelve month period prior to initiating treatment with acebilustat.