PPIDT00392

Drug Information
NameLanadelumab
SequenceEVQLLESGGGLVQPGGSLRLSCAASGFTFSHYIMMWVRQAPGKGLEWVSGIYSSGGITVYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAYRRIGVPRRDEFDIWGQGTMVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPG
DrugBank_IDDB14597
Typebiotech
IndicationLanadelumab is indicated for prophylaxis to prevent attacks in adult and pediatric patients aged 2 years and older with hereditary angioedema.[L45108,L49221] In Canada, it is indicated for use only in adults and adolescents.[L49226]

Dosage Forms
Form Route Strength
Injection, solution Parenteral; Subcutaneous
300 MG
Injection, solution Subcutaneous
150 mg
Injection, solution Subcutaneous
300 mg
Injection, solution Subcutaneous
300 mg/2mL
Solution Subcutaneous
150 mg/1mL
Solution Subcutaneous
300 mg/2mL
Solution Subcutaneous
300 mg / 2 mL
Injection, solution
300 mg/2ml
Target Information
Role Uniprot_ID Gene_Name Entity_Name Organism Actions Internal link
target P03952 KLKB1 Plasma kallikrein Homo sapiens inhibitor|regulator Link