Combination therapy for the treatment of cancer
Abstract
The present disclosure relates to a pharmaceutical combination comprising (1) a first agent which is a CDK inhibitor or a pharmaceutically acceptable salt thereof and (2) a second agent which is an anti-hormonal agent or a pharmaceutically acceptable salt thereof. The present disclosure also relates to a pharmaceutical combination comprising (1) a first agent which is a CDK inhibitor or a pharmaceutically acceptable salt thereof, (2) a second agent which is an anti-hormonal agent or a pharmaceutically acceptable salt thereof, and (3) a third agent which is an agent that regulates the PI3K/Akt/mTOR pathway or a pharmaceutically acceptable salt thereof.
Claims
exact text as granted — not AI-modified1 .- 29 . (canceled)
30 . A pharmaceutical combination comprising (1) a first agent which is Compound A1 described by Formula A1 below or a pharmaceutically acceptable salt thereof:
and (2) a second agent which is fulvestrant.
31 .- 42 . (canceled)
43 . A pharmaceutical combination consisting essentially of
(1) a first agent which is Compound A1 described by Formula A1 below or a pharmaceutically acceptable salt thereof:
and
(2) a second agent which is letrozole.
44 . The combination of claim 43 , wherein the agents are administered simultaneously, separately or sequentially.
45 . The combination of claim 43 , wherein the agents are administered simultaneously.
46 . The combination of claim 43 , wherein the agents are administered separately.
47 . The combination of claim 43 , wherein the agents are sequentially.
48 . A method of palliatively treating breast cancer consisting essentially of administering to a subject
(1) a first agent which is Compound A1 described by Formula A1 below or a pharmaceutically acceptable salt thereof:
and
(2) a second agent which is letrozole.
49 . The method of claim 48 , wherein the breast cancer is an estrogen receptor positive breast cancer.
50 . The method of claim 48 wherein the breast cancer is a HER2− breast cancer.
51 . The method of claim 48 , wherein the breast cancer is an estrogen receptor positive, HER2− breast cancer.
52 . The method of claim 48 , wherein the breast cancer is a hormone receptor positive, HER2− breast cancer.
53 . The method of claim 48 , wherein the agents are administered simultaneously.
54 . The method of claim 48 , wherein the agents are administered separately.
55 . The method of claim 48 , wherein the agents are sequentially.
56 . The method of claim 48 , wherein the breast cancer is an advanced breast cancer.
57 . The method of claim 56 , wherein the breast cancer is an estrogen receptor positive, HER2− advanced breast cancer.
58 . The method of claim 48 , wherein the breast cancer is a metastatic breast cancer.
59 . The method of claim 58 , wherein the breast cancer is an estrogen receptor positive, HER2− metastatic breast cancer.Join the waitlist — get patent alerts
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