Use of kinase inhibitors to manage tuberculosis and other infectious diseases
This disclosure relates to the use of kinase inhibitor to treat or prevent infectious diseases such as tuberculosis. In certain embodiments, this disclosure relates to treating or preventing an infectious disease comprising administering an effective amount of a kinase inhibitor or other compound disclosed herein to a subject in need thereof. In certain embodiments, the disclosure relates to methods of treating or preventing tuberculosis comprising administering a kinase inhibitor to a subject in need thereof. In certain embodiments, the subject is diagnosed with Mycobacterium tuberculosis (Mtb) that is resistant to multiple antibiotic agents.
1. A pharmaceutical product for use in the treatment of tuberculosis in the form of a tablet, capsule, or gel comprising imatinib in an amount of 50 to 400 mg in combination with ethambutol, isoniazid, pyrazinamide, rifabutin, rifampin, rifapentine, amikacin, capreomycin, cycloserine, ethionamide, levofloxacin, moxifloxacin, para-aminosalicylic acid, or streptomycin.
2. The pharmaceutical product of claim 1 wherein imatinib is in the amount of 50 to 100 mg.
3. The pharmaceutical product of claim 1 further comprising a carrier selected from dicalcium phosphate dihydrate, calcium sulfate, lactose, sucrose, mannitol, sorbitol, cellulose, microcrystalline cellulose, kaolin, sodium chloride, dry starch, hydrolyzed starches, pregelatinized starch, silicone dioxide, titanium oxide, magnesium aluminum silicate and a polysaccharide.
4. The pharmaceutical product of claim 1 wherein the tablet comprises an enteric coating.
5. The pharmaceutical product of claim 4 wherein the enteric coating comprises an excipient selected from hydroxypropyl cellulose, hydroxyethyl cellulose, hydroxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl methyl cellulose acetate succinate, hydroxypropyl methylcellulose phthalate, methylcellulose, ethyl cellulose, cellulose acetate, cellulose acetate phthalate, cellulose acetate trimellitate, and carboxymethylcellulose sodium.
6. A pharmaceutical product for use in the treatment of tuberculosis in the form of a tablet, capsule, or gel comprising imatinib in an amount of 50 to 400 mg in combination with bedaquiline.
7. The pharmaceutical product of claim 6 wherein imatinib is in the amount of 50 to 100 mg.
8. The pharmaceutical product of claim 6 further comprising a carrier selected from dicalcium phosphate dihydrate, calcium sulfate, lactose, sucrose, mannitol, sorbitol, cellulose, microcrystalline cellulose, kaolin, sodium chloride, dry starch, hydrolyzed starch, pregelatinized starch, silicone dioxide, titanium oxide, magnesium aluminum silicate and a polysaccharide.
9. The pharmaceutical product of claim 6 wherein the tablet comprises an enteric coating.
10. The pharmaceutical product of claim 9 wherein the enteric coating comprises an excipient selected from hydroxypropyl cellulose, hydroxyethyl cellulose, hydroxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl methyl cellulose acetate succinate, hydroxypropyl methylcellulose phthalate, methylcellulose, ethyl cellulose, cellulose acetate, cellulose acetate phthalate, cellulose acetate trimellitate, and carboxymethylcellulose sodium.
11. A pharmaceutical product for use in the treatment of tuberculosis in the form of a tablet, capsule, or gel comprising imatinib in an amount of 50 to 400 mg in combination with delamanid.
12. The pharmaceutical product of claim 11 wherein imatinib is in the amount of 50 to 100 mg.
13. The pharmaceutical product of claim 11 further comprising a carrier selected from dicalcium phosphate dihydrate, calcium sulfate, lactose, sucrose, mannitol, sorbitol, cellulose, microcrystalline cellulose, kaolin, sodium chloride, dry starch, hydrolyzed starch, pregelatinized starch, silicone dioxide, titanium oxide, magnesium aluminum silicate and a polysaccharide.
14. The pharmaceutical product of claim 11 , wherein the tablet comprises an enteric coating.
15. The pharmaceutical product of claim 14 wherein the enteric coating comprises an excipient selected from hydroxypropyl cellulose, hydroxyethyl cellulose, hydroxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl methyl cellulose acetate succinate, hydroxypropyl methylcellulose phthalate, methylcellulose, ethyl cellulose, cellulose acetate, cellulose acetate phthalate, cellulose acetate trimellitate, and carboxymethylcellulose sodium.