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BRACAnalysis CDx® is an in vitro diagnostic device intended for the qualitative detection and classification of variants in the protein-coding regions and intron/exon boundaries of the BRCA1 and BRCA2 genes using genomic DNA obtained from whole blood specimens collected in EDTA. Single nucleotide variants and small insertions and deletions (indels) are identified by polymerase chain reaction (PCR) and Sanger sequencing. Large deletions and duplications in BRCA1 and BRCA2 are detected using multiplex PCR. Results of the test are used as an aid in identifying ovarian cancer patients with deleterious or suspected deleterious germline BRCA variants eligible for treatment with Lynparza™ (olaparib). Patients who have undergone a previous allogeneic bone marrow transplant should not be tested with the BRACAnalysis CDx™ test.
Cancer:
Breast Cancer, Ovarian Cancer, Pancreatic Cancer, Prostate Cancer
Gene:
BRCA1 (Breast cancer 1, early onset), BRCA2 (Breast cancer 2, early onset)
Drug:
Lynparza (olaparib), Rubraca (rucaparib), Talzenna (talazoparib)
Method:
Multiplex-PCR
Approvals
Date
Cancer
Gene
Drug
By
12/19/14
FDA
01/12/18
FDA
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Confirmatory trial(s)