Zai Lab to Present Final OS Data from Phase 3 NORA Study of ZEJULA
In royalty dispute, UK appeals court sides with GSK over AZ
GSK`s cancer drug combination meets primary goal in late-stage trial
AKEEGA™ (niraparib and abiraterone acetate) Now Available from Onco360
Maintenance therapy with the PARP inhibitor niraparib (Zejula) prolonged progression-free survival (PFS) vs placebo in patients with newly diagnosed advanced ovarian cancer, according to findings from the phase 3 PRIME trial (NCT03709316) published in JAMA Oncology.­1
On August 11, 2023, the Food and Drug Administration approved the fixed dose combination of niraparib and abiraterone acetate (Akeega, Janssen Biotech, Inc.), with prednisone, for adult patients with deleterious or suspected deleterious BRCA-mutated castration-resistant prostate cancer (mCRPC), as determined by an FDA-approved test.
Janssen’s combination therapy of niraparib with abiraterone acetate plus prednisone for the treatment of BCRA-positive metastatic castration-resistant prostate cancer (mCRPC) is moving along.
In a phase 3 trial of Zejula in certain types of breast cancer, GSK’s bid to track tumor cells at the molecular level has helped patients catch metastatic disease before symptoms set in.
April 5 (Reuters) - A UK court on Wednesday ordered GSK's Tesaro to pay rival AstraZeneca (AZN.L) royalties on total sales of ovarian cancer drug Zejula, in a win for the Anglo-Swedish drugmaker.
Janssen Presents Updated Data Demonstrating Improved Outcomes from the Use of Niraparib in Combination with Abiraterone Acetate Plus Prednisone as a First-Line Therapy in Patients with BRCA-Positive Metastatic Castration-Resistant Prostate Cancer