Thymosin alpha 1 for use in treatment of cystic fibrosis
View Patent ↗The present invention concerns Thymosin alpha 1 for use in treatment of cystic fibrosis as a CFTR corrector, CFTR potentiator and anti-inflammatory agent.
1. A method of treating cystic fibrosis in a patient comprising administering a pharmaceutical composition comprising Thymosin alpha 1 to the patient, wherein the patient has a cystic fibrosis transmembrane conductance regulator (CFTR) mutation ΔF508.
2. The method according to claim 1 , wherein the composition comprises a combination of Thymosin alpha 1 with at least one agent selected from the group consisting of antibiotic, antifungal, Cystic fibrosis transmembrane conductance regulator (CFTR) corrector, and CFTR potentiator agent, wherein said CFTR corrector or potentiator being other than Thymosin alpha 1.
3. The method according to claim 2 , wherein said at least one antibiotic agent is selected from the group consisting of tobramycin, ciprofloxacin, and colistin.
4. The method according to claim 2 , wherein said at least one antifungal agent is selected from the group consisting of itraconazole and amphotericin B.
5. The method according to claim 2 , wherein said at least one CFTR corrector or potentiator agent other than Thymosin alpha 1 is selected from the group consisting of Ivacaftor and Lumacaftor.
6. The method according to claim 1 , wherein the pharmaceutical composition comprises one or more excipients and/or coadjuvants.
7. The method according to claim 1 , wherein the method consists of administering a pharmaceutical composition comprising Thymosin alpha 1 to the patient, wherein Thymosin alpha 1 is the only active principle in the composition.
8. The method according to claim 2 , wherein Thymosin alpha 1 and said at least one agent selected from the group consisting of antibiotic, antifungal, CFTR corrector, and CFTR potentiator agent are administered to the patient together, separately, or sequentially.
9. The method according to claim 1 , wherein the treatment prevents chronic inflammation in patients affected by cystic fibrosis.
10. A method of treating cystic fibrosis (CF) in a patient, wherein the patient has a cystic fibrosis transmembrane conductance regulator (CFTR) mutation ΔF508 (ΔF508-CFTR), the method comprises administering a pharmaceutical composition comprising Thymosin alpha 1 to the patient, wherein the treatment is intended to cause one or more effects selected from the group consisting of:
(1) increasing cell surface expression of ΔF508-CFTR in CF cells of the patient;
(2) increasing the functional activity of ΔF508-CFTR in CF cells of the patient; and
(3) inducing the expression of alternative ion channel TMEM16A in the patient.