Patent classifications
A61K38/55
Therapy for the Treatment of Cancer
Provided herein are methods of treating and/or managing cancer, which comprise administering to a patient Compound A, or an enantiomer or a mixture of enantiomers thereof, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph thereof. Additionally, provided herein are methods of treating and/or managing cancer, which comprise administering to a patient Compound A, or an enantiomer or a mixture of enantiomers thereof, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph thereof, in combination with a second agent selected from the group consisting of an anti-CD20 antibody, an HDAC inhibitor, a proteasome inhibitor, an anti-CD38 antibody, an anti-SLAMF7 antibody, a nuclear export inhibitor, a BCL-2 inhibitor, and an immune checkpoint inhibitor. Also provided herein are combination therapies for treating and/or managing cancer, which further comprise dexamethasone as a third agent.
Therapy for the Treatment of Cancer
Provided herein are methods of treating and/or managing cancer, which comprise administering to a patient Compound A, or an enantiomer or a mixture of enantiomers thereof, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph thereof. Additionally, provided herein are methods of treating and/or managing cancer, which comprise administering to a patient Compound A, or an enantiomer or a mixture of enantiomers thereof, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph thereof, in combination with a second agent selected from the group consisting of an anti-CD20 antibody, an HDAC inhibitor, a proteasome inhibitor, an anti-CD38 antibody, an anti-SLAMF7 antibody, a nuclear export inhibitor, a BCL-2 inhibitor, and an immune checkpoint inhibitor. Also provided herein are combination therapies for treating and/or managing cancer, which further comprise dexamethasone as a third agent.
Protease Inhibitors for Treatment of Coronavirus Infections
- Arnab K. Chatterjee ,
- Jian Jeffrey Chen ,
- Elshan Nakath ,
- Alireza Rahimi ,
- Anil Kumar Gupta ,
- Gennadii Grabovyi ,
- Katy Wilson ,
- Sourav Ghorai ,
- Armen Nazarian ,
- James Pedroarena ,
- Wrickban Mazumdar ,
- Frank Weiss ,
- Lirui Song ,
- Malina A. Bakowski ,
- Laura Riva ,
- Karen Wolff ,
- Case W. McNamara ,
- Thomas F. Rogers ,
- Jacqueline Malvin ,
- Shuangwei Li ,
- Sean Joseph ,
- Ashley Woods ,
- Yuyin Liu ,
- Neechi Okwor
Provided herein are compounds of Formula (I), their pharmaceutically acceptable salts, and their pharmaceutical compositions:
##STR00001##
wherein R.sup.1, R.sup.2, R.sup.3a, R.sup.3b, R.sup.4, R.sup.5, and A are defined in the present disclosure. The compounds are potent inhibitors of the main protease (M.sup.pro) of severe acute respiratory syndrome Coronavirus-2 (SARS-CoV-2), and they are useful in treating or preventing COVID-19 in a subject.
Protease Inhibitors for Treatment of Coronavirus Infections
- Arnab K. Chatterjee ,
- Jian Jeffrey Chen ,
- Elshan Nakath ,
- Alireza Rahimi ,
- Anil Kumar Gupta ,
- Gennadii Grabovyi ,
- Katy Wilson ,
- Sourav Ghorai ,
- Armen Nazarian ,
- James Pedroarena ,
- Wrickban Mazumdar ,
- Frank Weiss ,
- Lirui Song ,
- Malina A. Bakowski ,
- Laura Riva ,
- Karen Wolff ,
- Case W. McNamara ,
- Thomas F. Rogers ,
- Jacqueline Malvin ,
- Shuangwei Li ,
- Sean Joseph ,
- Ashley Woods ,
- Yuyin Liu ,
- Neechi Okwor
Provided herein are compounds of Formula (I), their pharmaceutically acceptable salts, and their pharmaceutical compositions:
##STR00001##
wherein R.sup.1, R.sup.2, R.sup.3a, R.sup.3b, R.sup.4, R.sup.5, and A are defined in the present disclosure. The compounds are potent inhibitors of the main protease (M.sup.pro) of severe acute respiratory syndrome Coronavirus-2 (SARS-CoV-2), and they are useful in treating or preventing COVID-19 in a subject.
Composition comprising highly-concentrated α1 proteinase inhibitor and method for obtaining thereof
Compositions include highly-concentrated Alpha-1 Proteinase Inhibitor (A1PI) in a concentration greater than or equal to 100 mg/ml. Pharmaceutical compositions can be prepared from these compositions. The pharmaceutical compositions can be suitable for subcutaneous administration. The highly-concentrated A1PI solutions can be obtained by single-pass tangential flow filtration (SPTFF).
Composition comprising highly-concentrated α1 proteinase inhibitor and method for obtaining thereof
Compositions include highly-concentrated Alpha-1 Proteinase Inhibitor (A1PI) in a concentration greater than or equal to 100 mg/ml. Pharmaceutical compositions can be prepared from these compositions. The pharmaceutical compositions can be suitable for subcutaneous administration. The highly-concentrated A1PI solutions can be obtained by single-pass tangential flow filtration (SPTFF).
CASPASE INHIBITORS TO ENHANCE INJURY REPAIR AND TO TREAT BACTERIAL AND VIRAL INFECTIONS
The present invention relates to the field of caspase inhibition. More specifically, the present invention provides compositions and methods utilizing caspase inhibitors to enhance injury repair and to treat bacterial and viral infections. In a specific embodiment, a method for treating a bacterial infection and skin lesions in a patient comprises the step of administering to the patient an effective amount of a caspase inhibitor.
METHODS AND COMPOSITIONS FOR TREATING DIABETES
Described herein are methods and compositions for treating diabetes mellitus, concerning oral pharmaceutical compositions comprising insulin in combination with a GLP-1 analogue.
METHODS AND COMPOSITIONS FOR TREATING DIABETES
Described herein are methods and compositions for treating diabetes mellitus, concerning oral pharmaceutical compositions comprising insulin in combination with a GLP-1 analogue.
METHODS AND COMPOSITIONS FOR TREATING DIABETES
Described herein are methods and compositions for treating diabetes mellitus, concerning oral pharmaceutical compositions comprising insulin in combination with a GLP-1 analogue.