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Status:
Possibly Marketed Outside US
Source:
21 CFR 333A
(2020)
Source URL:
First approved in 2020
Source:
21 CFR 333A
Source URL:
Class:
CONCEPT
Status:
Possibly Marketed Outside US
Source:
21 CFR 333A
(2020)
Source URL:
First approved in 2020
Source:
21 CFR 333A
Source URL:
Class:
CONCEPT
Status:
Possibly Marketed Outside US
Source:
Sunburst Orange Betta by GloFish LLC
(2020)
Source URL:
First approved in 2020
Source:
Sunburst Orange Betta by GloFish LLC
Source URL:
Class:
CONCEPT
Status:
Possibly Marketed Outside US
Source:
Sunburst Orange Barb by GloFish LLC
(2020)
Source URL:
First approved in 2020
Source:
Sunburst Orange Barb by GloFish LLC
Source URL:
Class:
CONCEPT
Status:
Possibly Marketed Outside US
Source:
Galactic Purple Barb by GloFish LLC
(2020)
Source URL:
First approved in 2020
Source:
Galactic Purple Barb by GloFish LLC
Source URL:
Class:
CONCEPT
Status:
Possibly Marketed Outside US
Source:
Electric Green Betta by GloFish LLC
(2020)
Source URL:
First approved in 2020
Source:
Electric Green Betta by GloFish LLC
Source URL:
Class:
CONCEPT
Status:
Possibly Marketed Outside US
Source:
M020
(2024)
Source URL:
First approved in 2020
Source:
21 CFR 333A
Source URL:
Class:
CONCEPT
Status:
Possibly Marketed Outside US
Source:
NDA211988
(2021)
Source URL:
First approved in 2020
Source:
21 CFR 333A
Source URL:
Class:
CONCEPT
Status:
US Approved Rx
(2020)
Source:
NDA213721
(2020)
Source URL:
First approved in 2020
Source:
NDA213721
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Targets:
Conditions:
Pralsetinib (GAVRETO™, Blueprint Medicines Corporation) is an orally-administered, next-generation, small-molecule selective rearranged during transfection (RET) inhibitor being developed for the treatment of various solid tumours. RET is a well described proto-oncogene present in multiple cancers including non-small cell lung cancer (NSCLC), papillary thyroid cancer, and medullary thyroid carcinoma. Pralsetinib is a kinase inhibitor of wild-type RET and oncogenic RET fusions (CCDC6-RET)
and mutations (RET V804L, RET V804M and RET M918T) with half maximal inhibitory
concentrations (IC50s) less than 0.5 nM. In purified enzyme assays, pralsetinib inhibited DDR1, TRKC, FLT3, JAK1-2, TRKA, VEGFR2, PDGFRb, and FGFR1 at higher concentrations that were still clinically achievable at Cmax. In cellular assays, pralsetinib inhibited RET at approximately 14-, 40-, and 12-fold lower concentrations than VEGFR2, FGFR2, and JAK2, respectively. Pralsetinib is approved for the treatment of RET fusion-positive metastatic NSCLC. In the pivotal phase I/II ARROW trial, pralsetinib demonstrated rapid and durable anti-tumour activity in patients with advanced RET fusion-positive NSCLC who were previously treated with platinum-based chemotherapy or were treatment-naïve. Pralsetinib also showed clinical activity against intracranial metastases arising from NSCLC. Pralsetinib had a manageable tolerability profile, with the most common grade 3 treatment-related adverse events being neutropenia, hypertension, anaemia and decreased white blood cell count.
Status:
US Approved Rx
(2020)
Source:
NDA214094
(2020)
Source URL:
First approved in 2020
Source:
NDA214094
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Targets:
Conditions:
Berotralstat (ORLADEYO™; BCX7353) is an orally administered kallikrein inhibitor, which has been developed by BioCryst Pharmaceuticals for hereditary angioedema (HAE). The inhibition of kallikrein by berotralstat decreases the production of bradykinin, which prevents the localised tissue oedema that occurs during attacks of HAE. Berotralstat has been approved in the USA, and subsequently in Japan, for prophylaxis to prevent attacks of HAE in adults and paediatric patients aged 12 years or older.