US2023240987A1PendingUtilityA1
Methods of treatment of viral diseases
Est. expiryMay 28, 2040(~13.9 yrs left)· nominal 20-yr term from priority
A61K 9/0078A61K 9/08A61K 31/706A61K 47/10A61M 2202/0468A61M 2202/206A61M 11/007A61M 15/0065A61M 2205/8281A61P 31/14A61M 2202/04B05B 11/026B05B 11/1091
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Claims
Abstract
The present invention provides for a method for the treatment of a viral disease, disorder or condition in a subject, the method comprising the step of administering to said subject a medically active liquid in nebulized form by inhalation, wherein the medically active liquid comprises remdesivir or a pharmaceutically acceptable salt thereof and wherein the medically active liquid is administered in nebulized form using an inhalation device.
Claims
exact text as granted — not AI-modified1 . A method for the treatment or prevention of a viral infection or viral disease, disorder or condition in a subject, the method comprising the step of administering to said subject a medically active liquid in nebulized form by inhalation, wherein the medically active liquid comprises remdesivir or a pharmaceutically acceptable salt thereof, and wherein the medically active liquid is administered to the subject in nebulized form by inhalation using an inhalation device.
2 . The method according to claim 1 , wherein the viral infection or viral disease, disorder or condition is a coronavirus infection or a coronavirus disease, disorder or condition.
3 . The method according to claim 2 , wherein the coronavirus infection is a SARS-CoV or SARS-CoV-2 infection or the coronavirus disease, disorder or condition results from a SARS-CoV or SARS-CoV-2 infection.
4 . The method according to claim 2 , wherein the coronavirus infection is a Middle East respiratory syndrome coronavirus infection or the coronavirus disease, disorder or condition results from a Middle East respiratory syndrome coronavirus infection.
5 . The method according to claim 1 , wherein the viral infection or viral disease, disorder or condition is one which is responsive to inhibition of viral replication.
6 . The method according to claim 1 , wherein the viral disease, disorder or condition is a disease, disorder or condition of the immune system; an inflammatory disease, disorder or condition; an autoimmune disease, disorder or condition; a disease, disorder or condition of the cardiovascular system; a cancer; a tumor or other malignancy; a disease, disorder or condition of the renal system; a disease, disorder or condition of the gastro-intestinal tract; a disease, disorder or condition of the respiratory system; a disease, disorder or condition of the endocrine system; and/or a disease, disorder or condition of the central nervous system (CNS).
7 . The method according to claim 1 , wherein the viral disease, disorder or condition is an inflammatory disease, disorder or condition.
8 . The method according to claim 1 , wherein the viral disease, disorder or condition is a severe acute respiratory syndrome (SARS).
9 . (canceled)
10 . (canceled)
11 . (canceled)
12 . The method according to claim 1 , wherein the subject is a human or animal.
13 . The method according to claim 1 , wherein the subject is diagnosed with a viral infection or viral disease, disorder or condition.
14 . The method according to claim 13 , wherein the subject is diagnosed with COVID-19.
15 . (canceled)
16 . (canceled)
17 . The method according to claim 1 , wherein the inhalation device used to administer the medically active liquid comprising the remdesivir or a pharmaceutically acceptable salt thereof is a soft-mist-inhaler.
18 . The method according to claim 1 , wherein the inhalation device used to administer the medically active liquid comprising the remdesivir or a pharmaceutically acceptable salt thereof is a soft-mist-inhaler having at least one impingement-type nozzle.
19 . The method according to claim 1 , wherein the inhalation device used to administer the medically active liquid comprising remdesivir or a pharmaceutically acceptable salt thereof is a hand-held inhalation device for delivering a nebulised medically active aerosol for inhalation therapy, comprising
(a) a housing having a user-facing side; (b) an impingement-type nozzle for generating the nebulised aerosol by collision of at least two liquid jets, the nozzle being firmly affixed to the user-facing side of the housing such as to be immobile relative to the housing; (c) a fluid reservoir arranged within the housing; and (d) a pumping unit arranged within the housing, the pumping unit having
an upstream end that is fluidically connected to the fluid reservoir;
a downstream end that is fluidically connected to the nozzle;
wherein the pumping unit is adapted for pumping fluid from the fluid reservoir to the nozzle; wherein the pumping unit further comprises
(i) a riser pipe having an upstream end, wherein the riser pipe is
adapted to function as a piston in the pumping unit, and
firmly affixed to the user-facing side of the housing such as to be immobile relative to the housing; and
(ii) a hollow cylinder located upstream of the riser pipe, wherein the upstream end of the riser pipe is inserted in the cylinder such that the cylinder is longitudinally movable on the riser pipe;
(iii) a lockable means for storing potential energy when locked and for releasing the stored energy when unlocked, the means being arranged outside of, and mechanically coupled to, the cylinder such that unlocking the means results in a propulsive longitudinal movement of the cylinder towards the downstream end of the pumping unit.
20 . The method according to claim 1 , wherein the medically active liquid comprises a concentration of remdesivir of about 10 μg/μL to about 30 μg/μL.
21 . (canceled)
22 . The method according to claim 1 , wherein the administered medically active liquid comprises about 150 μg to about 230 μg of remdesivir.
23 . The method according to claim 22 , wherein the administered medically active liquid comprises about 225 μg of remdesivir.
24 . The method according to claim 1 , wherein an average particle size distribution of the medically active liquid has a particle size Dv50 value of about 2.0 μm to about 4.0 μm.
25 . The method according to claim 1 , wherein the medically active liquid comprises an alcohol.
26 . The method according to claim 25 , wherein the alcohol is ethanol.Cited by (0)
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