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Status:
US Approved Rx
(2022)
Source:
NDA208712
(2022)
Source URL:
First approved in 2022
Source:
NDA208712
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Pacritinib (SB1518), discovered in Singapore at the labs of S*BIO Pte Ltd., is an oral tyrosine kinase inhibitor (TKI) with activity against two important activating mutations: Janus Associated Kinase 2 (JAK2) and FMS-like tyrosine kinase 3 (FLT3). The JAK family of enzymes is a central component in signal transduction pathways, which are critical to normal blood cell growth and development as well as inflammatory cytokine expression and immune responses. Activating mutations of JAK2 are implicated in certain blood-related cancers, including myeloproliferative neoplasms (MPNs), leukemia and certain solid tumors. FLT3 is a gene commonly found mutated in patients with acute myeloid leukemia (AML). Pacritinib has demonstrated encouraging results in Phase 1 and 2 studies for patients with myelofibrosis and may offer an advantage over other JAK inhibitors through effective treatment of symptoms while having less treatment-emergent thrombocytopenia and anemia than has been seen in currently approved and in-development JAK inhibitors. Pacritinib is acquired by Cell Therapeutics, Inc. (CTI) and Baxter international and could effectively address an unmet medical need for patients living with myelofibrosis who face treatment-emergent thrombocytopenia on marketed JAK inhibitors. Currently Pacritinib is undergoing preregistration for myelofibrosis.
Status:
US Approved Rx
(2022)
Source:
NDA216340
(2022)
Source URL:
First approved in 2022
Source:
NDA216340
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Status:
US Approved Rx
(2022)
Source:
NDA215974
(2022)
Source URL:
First approved in 2022
Source:
NDA215974
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Status:
US Approved Rx
(2022)
Source:
NDA215814
(2022)
Source URL:
First approved in 2022
Source:
NDA215814
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Status:
US Approved Rx
(2022)
Source:
NDA214958
(2022)
Source URL:
First approved in 2022
Source:
NDA214958
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
US Approved Rx
(2022)
Source:
NDA215833
(2022)
Source URL:
First approved in 2022
Source:
NDA215833
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Status:
US Approved Rx
(2022)
Source:
NDA214985
(2022)
Source URL:
First approved in 2022
Source:
NDA214985
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Status:
US Approved Rx
(2022)
Source:
NDA216196
(2022)
Source URL:
First approved in 2022
Source:
NDA216196
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Conditions:
Mitapivat, also known as PKM2 activator 1020, is an activator of a pyruvate kinase PKM2, an enzyme involved in glycolysis. It was disclosed in a patent publication WO 2011002817 A1 as compound 78.
Status:
US Approved Rx
(2022)
Source:
NDA216986
(2022)
Source URL:
First approved in 2022
Source:
NDA216986
Source URL:
Class (Stereo):
CHEMICAL (MIXED)
Status:
US Approved Rx
(2023)
Source:
NDA214373
(2023)
Source URL:
First approved in 2022
Source:
NADA141566
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Targets:
Conditions:
Bexagliflozin, also known as EGT1442, is a potent and selective SGLT2 inhibitor. Bexagliflozin is under investigation for the treatment of Type 2 Diabetes Mellitus. Bexagliflozin has been investigated for the treatment of Diabetes Mellitus and Type2 Diabetes Mellitus. Clinical studies have established that bexagliflozin significantly reduces blood glucose and glycated hemoglobin in subjects with diabetes. Treatment with bexagliflozin also induces weight loss and a reduction in systolic and diastolic blood pressure.