Inhalable rapamycin formulation for the treatment of pulmonary hypertension
The present invention relates to methods and compositions for the treatment and prophylaxis of pulmonary arterial hypertension (PAH) in a human subject in need of such treatment, the methods comprising the pulmonary administration to the subject, preferably via inhalation of a composition comprising rapamycin or a prodrug or derivative thereof.
1. A method for the treatment of pulmonary arterial hypertension (PAH) in a human subject in need of such treatment, the method comprising administering to the subject by inhalation a pharmaceutical dry powder composition comprising micronized rapamycin particles and particles of a carrier, wherein the micronized rapamycin particles have a Mass Median Aerodynamic Diameter (MMAD) of from 2-3 microns, wherein the composition is effective to deliver a therapeutic amount of the microparticulate rapamycin to the lungs of the human subject, and wherein rapamycin is the only therapeutic agent in the composition.
2. The method of claim 1 , wherein the administering is once daily or twice daily by inhalation.
3. The method of claim 1 , wherein the administering is performed using a dry powder delivery device comprising a reservoir containing a unit dosage form of the pharmaceutical dry powder composition.
4. The method of claim 3 , wherein the unit dosage form contains from 50-150 micrograms of rapamycin.
5. The method of claim 3 , wherein the unit dosage form is a capsule suitable for use in the dry powder inhaler device.
6. The method of claim 5 , wherein the capsule is a gelatin, plastic, polymeric, or cellulosic capsule.
7. The method of claim 3 , wherein the unit dosage form is in the form of a foil/foil or foil/plastic blister.
8. The method of claim 1 , wherein the carrier is a saccharide or a sugar alcohol.
9. The method of claim 1 , wherein the carrier is selected from the group consisting of arabinose, glucose, fructose, ribose, mannose, sucrose, trehalose, lactose, maltose, a starch, dextran, mannitol, xylitol, and mixtures of any of the foregoing.
10. The method of claim 1 , wherein the carrier comprises a blend of two different carriers, a first carrier and a second carrier.
11. The method of claim 10 , wherein the first carrier consists of particles having diameters of from 30-100 microns and the second carrier consists of particles having diameters of less than 10 microns.
12. The method of claim 1 , wherein the carrier does not comprise albumin.
13. The method of claim 1 , wherein the carrier is not a carrier protein.
14. The method of claim 1 , wherein the micronized rapamycin particles are dispersed onto the surface of particles of the carrier.