Find product and prescribing information, as well as other resources, for Genentech’s rare blood disorder portfolio below.
(emicizumab-kxwh)
Safety Data Sheets:
Visit PubMed.gov to view scientific literature for Genentech rare blood disorder portfolio products.
Hemlibra® at PubMed.gov
Genentech maintains a presence at in-person and virtual scientific congresses worldwide. Find Genentech-sponsored posters and presentations from recent congresses at Medically.gene.com.
Find information about active clinical research for Genentech rare blood disorder portfolio products.
Hemlibra® at ClinicalTrials.gov
Connect with a Medical Science Liaison
Browse the Genentech Medical Information Library
Visit emicizumabinfo.com, a different Genentech medical website, for key Hemlibra® safety topics
The BrandX™ Co-pay Card Program may help lower the out-of-pocket costs for your patients.
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Ab: antibody
AE: adverse event
ASTCT: American Society for Transplantation and Cellular Therapy
CR: complete response
CRS: cytokine release syndrome
CT: computed tomography
CTCAE: Common Terminology Criteria for Adverse Events
DoR: duration of response
ECOG PS: Eastern Cooperative Oncology Group performance status
FL: follicular lymphoma
ICANS: immune effector cell-associated neurotoxicity syndrome
IRF: independent review facility
IV: intravenous
IQR: interquartile range
NCI CTCAE: National Center Institute Common Terminology Criteria for Adverse Events
NHL: non-Hodgkin lymphoma
ORR: objective response rate
PET: positron emission tomography
PFS: progression-free survival
PR: partial response
R/R: relapsed/refractory
SAE: serious adverse event
SD: stable disease
USPI: United States Prescribing Information
UTI: urinary tract infection
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