US2016346246A1PendingUtilityA1
Methods for the treatment of lung diseases with mast cell stabilizers
Est. expiryFeb 10, 2034(~7.6 yrs left)· nominal 20-yr term from priority
A61P 37/08A61P 11/06A61P 11/00A61K 9/0073A61K 47/02A61K 9/0075A61K 9/12A61K 9/0078A61K 9/08A61K 31/352A61K 47/183
54
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Claims
Abstract
Methods for the treatment of lung diseases with mast cell stabilizers are provided.
Claims
exact text as granted — not AI-modified1 - 55 . (canceled)
56 . A pharmaceutically acceptable aerosol, comprising droplets of a solution comprising from about 2% to about 6% by weight of cromolyn sodium and an osmolarity adjusting agent consisting of sodium chloride.
57 . The pharmaceutically acceptable aerosol of claim 56 , wherein said solution further comprises purified water and sodium EDTA.
58 . The pharmaceutically acceptable aerosol of claim 56 or 57 , wherein said solution comprises from about 5 mg to about 80 mg of cromolyn sodium.
59 . The pharmaceutically acceptable aerosol of claim 56 or 57 , wherein said solution comprises from about 36 mg to about 44 mg of cromolyn sodium.
60 . The pharmaceutically acceptable aerosol of claim 56 or 57 , wherein said aerosol has a respirable fraction (≦3.3 μm) as measured by USP <1601> of at least about 30%.
61 . The pharmaceutically acceptable aerosol of claim 56 or 57 , wherein said aerosol has a respirable fraction (≦3.3 μm) as measured by USP <1601> of at least about 30% and a respirable fraction (≦5 μm) as measured by USP <1601> of at least about 75%.
62 . The pharmaceutically acceptable aerosol of claim 56 or 57 , wherein said osmolarity adjusting agent consists of between 0.1% to 0.7% sodium chloride, inclusive of the endpoints.
63 . The pharmaceutically acceptable aerosol of claim 56 or 57 , wherein said osmolarity adjusting agent consists of between 0.1% to 0.2% sodium chloride, inclusive of the endpoints.Cited by (0)
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