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Status:
US Approved Rx
(2002)
Source:
BLA103946
(2002)
Source URL:
First approved in 2002
Source:
BLA103946
Source URL:
Class:
PROTEIN
Status:
US Approved Rx
(2001)
Source:
BLA103949
(2001)
Source URL:
First approved in 2001
Source:
BLA103949
Source URL:
Class:
PROTEIN
Status:
US Approved Rx
(2001)
Source:
BLA103950
(2001)
Source URL:
First approved in 2001
Source:
BLA103950
Source URL:
Class:
PROTEIN
Status:
US Approved Rx
(2001)
Source:
BLA103948
(2001)
Source URL:
First approved in 2001
Source:
BLA103948
Source URL:
Class:
PROTEIN
Status:
US Approved Rx
(2001)
Source:
BLA103951
(2001)
Source URL:
First approved in 2001
Source:
BLA103951
Source URL:
Class:
PROTEIN
Status:
US Approved Rx
(2019)
Source:
NDA211215
(2019)
Source URL:
First approved in 2000
Source:
NDA020873
Source URL:
Class:
PROTEIN
Targets:
Conditions:
Bivalirudin is a synthetic 20 amino acid peptide rationally designed based on structural studies of hirudin, a naturally occurring anticoagulant. Bivalirudin is sold under the brand name Angiomax and is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA). It is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin. Bivalirudin directly inhibits thrombin by binding simultaneously to its active catalytic site and its substrate recognition site.
Status:
US Approved Rx
(2017)
Source:
BLA761060
(2017)
Source URL:
First approved in 2000
Source:
Mylotarg
Source URL:
Class:
PROTEIN
Status:
US Approved Rx
(2000)
Source:
BLA020986
(2000)
Source URL:
First approved in 2000
Source:
BLA020986
Source URL:
Class:
PROTEIN
Targets:
Conditions:
Insulin aspart, a human insulin analogue, is a rapid-acting, parenteral blood glucose-lowering agent. Insulin aspart was marketed under the brand name NovoLog for the treatment of adult patients with diabetes mellitus, for the control of hyperglycemia. The primary activity of the drug is the regulation of glucose metabolism. Insulin aspart binds to the insulin receptors on muscle and fat cells and lower blood glucose by facilitating the cellular uptake of glucose and simultaneously inhibiting the output of glucose from the liver. This drug has an off-label treatment for gestational diabetes (temporary diabetes caused by diabetes).
Status:
US Approved Rx
(2015)
Source:
BLA205692
(2015)
Source URL:
First approved in 2000
Source:
BLA021081
Source URL:
Class:
PROTEIN
Targets:
Insulin glargine, a long-acting form of insulin, was marketed under the brand name LANTUS. Lantus is indicated for the treatment of adult and pediatric patients with type 1 diabetes mellitus or adult patients with type 2 diabetes mellitus who require basal (long-acting) insulin for the control of hyperglycemia. The primary activity of insulin glargine is regulation of glucose metabolism. It lowers blood glucose levels by stimulating peripheral glucose uptake, especially by skeletal muscle and fat, and by inhibiting hepatic glucose production. The off-label use of insulin glargine is the treatment type 2 diabetes in children and the treatment of gestational diabetes.
Status:
US Approved Rx
(2000)
Source:
BLA103909
(2000)
Source URL:
First approved in 2000
Source:
BLA103909
Source URL:
Class:
PROTEIN