FDA Approves Entrectinib for the Treatment of NTRK Fusion-Positive Solid Tumours in Adult and Adolescent Patients
It also approvesentrectinibfor the treatment of ROS1-positive metastatic NSCLC in adults
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It also approvesentrectinibfor the treatment of ROS1-positive metastatic NSCLC in adults
Social media platforms provide the opportunity for virtual dialogue between patients and caregivers
Building evidence for genomic sequencing
It is the first systemic therapy approved for patients with this tumour
An in-depth re-analysis of recommendations beyond the FDA-approved indications
EU regulatory initiative aims to make a clearer distinction between liposomal and non-liposomal formulations of the same active substance
Approval is based on evidence from the ARAMIS study
FDA also approved a new use for the PD-L1 IHC 22C3 pharmDx kit as a companion diagnostic
T cell clones that may have just recently entered the tumour may be a cause for T cell response to immune checkpoint inhibitors
The change concerned an extension of indications to previously untreated patients with severe aplastic anaemia from 2 years of age
New indication concerns a combination with axitinib for the first-line treatment of advanced renal cell carcinoma
New indication concerns a combination with pomalidomide and dexamethasone for the treatment of adult patients with relapsed and refractory multiple myeloma
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