Modulators of ATP-binding cassette-transporters
Compounds of the present invention, and pharmaceutically acceptable compositions thereof, are useful as modulators of ATP-Binding Cassette (“ABC”) transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator (“CFTR”). The present invention also relates to methods of treating ABC transporter mediated diseases using compounds of the present invention.
1. A method of treating or lessening the severity of a disease in a patient, wherein the disease is cystic fibrosis comprising the step of administering to the patient an effective amount of a compound
wherein the patient has a defective gene that causes a deletion of phenylalanine at position 508 of the cystic fibrosis transmembrane conductance regulator amino acid sequence.
2. The method of claim 1 , wherein the patient has two copies of the defective gene.
3. A method of treating or lessening the severity of cystic fibrosis in a patient, wherein the patient has a defective gene that causes a deletion of phenylalanine at position 508 of the cystic fibrosis transmembrane conductance regulator amino acid sequence, said method comprising the step of administering to said patient an effective amount of a composition comprising:
i) the compound:
or a pharmaceutically acceptable salt thereof; and
ii) a pharmaceutically acceptable carrier.
4. The method of claim 3 , wherein the patient has two copies of the defective gene.
5. The method of claim 3 or 4 , wherein the composition further comprises a mucolytic agent, a bronchodialator, an antibiotic, an anti-infective agent, an anti-inflammatory agent, a CFTR modulator, or a nutritional agent.
6. The method of claim 3 or 4 , wherein the composition further comprises a CFTR modulator.