First study niraparib
WebMar 21, 2024 · The PRIMA study previously conducted by Zai Lab’s partner GlaxoSmithKline plc (GSK) demonstrated that niraparib conferred a PFS benefit to … WebJul 2, 2024 · Study Description Go to Brief Summary: This study will evaluate the efficacy and safety of niraparib and novel treatment combinations of niraparib as described …
First study niraparib
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Web• Conduct clinical data review on Medidata Rave ® for the FIRST study (dostarlimab and niraparib as First-line Treatment of Stage III or IV … WebOct 29, 2024 · European Commission approves Zejula (niraparib) as first-line monotherapy maintenance treatment in advanced ovarian cancer . For media and investors only. ...
WebTime to First Subsequent Therapy (TFST) and Progression-Free Survival 2 (PFS2) From the Phase 3 Randomized, Double-Blind PRIMA/ENGOT-V26/GOG-3012 Study in Patients With Newly Diagnosed Ovarian Cancer ... • Niraparib significantly improved PFS in patients with HRd tumors and in the overall population 1L, first-line; CI, confidence interval; CT ... WebNiraparib is marketed in the United States and Europe under the trade name Zejula ®. About PRIMA. PRIMA is a double-blind, randomised Phase 3 study designed to evaluate niraparib versus placebo in first-line Stage III or IV ovarian cancer patients.
Web1 day ago · Niraparib, or the MAGNITUDE trial, looked at patients with metastatic CRPC for first-line therapy randomized to either ARPI or abiraterone versus abiraterone plus niraparib. Now, what's different of the MAGNITUDE study compared to the other two that have been recently reported now is that it had a prospective selection of the patients ... WebThe study was conducted in accordance with the eth-ical standards of the Declaration of Helsinki, and the ... ZEJULAR (Niraparib) for First-Line Maintenance Treat-mentofOvarianCancerinChina[Internet].GlobeNewswire News Room. 2024 [cited 2024 May 17]. Available from:
WebApr 11, 2024 · Of the total 142 patients, 93 received niraparib as first-line maintenance therapy, 31 as maintenance therapy for platinum-sensitive recurrent ovarian cancer, and 18 as salvage treatment. ... The study was conducted in accordance with the ethical standards of the Declaration of Helsinki, and the ethics committee of the main study center Fudan ...
WebFeb 16, 2024 · Chi et al. Phase 3 MAGNITUDE study: First results of niraparib (NIRA) with abiraterone acetate and prednisone (AAP) as first-line therapy in patients (pts) with metastatic castration-resistant prostate cancer (mCRPC) with and without homologous recombination repair (HRR) gene alterations. ASCO GU 2024. csharp tftp serverWebSep 3, 2024 · The primary strength of this study is that it represents one of the first investigations of a PARP inhibitor with a PD-1 inhibitor for the first-line treatment of NSCLC. Niraparib in combination with pembrolizumab … csharp textwriterWebPRIMA is a double-blind, randomised Phase 3 study designed to evaluate niraparib versus placebo in first-line Stage III or IV ovarian cancer patients. The study assessed the … ea form hilangWebSep 6, 2024 · The study had a single arm: All participants were prescribed niraparib 300 mg per day, which was given as oral capsules. In order to assess the effectiveness of … csharp thisWebJan 1, 2024 · This study f … The JASPER clinical trial studied a new combination treatment for advanced or metastatic non-small cell lung cancer (NSCLC). ... ≥50% (cohort 1) or 1%-49% (cohort 2) received first-line niraparib (200 mg once daily) plus pembrolizumab (200 mg every 3 weeks). The primary end point was investigator-assessed objective response ... ea form lhdn 2022WebNov 30, 2024 · A study of niraparib combined with MGD013 in patients with advanced or metastatic solid tumor who failed prior treatment. clinicaltrials.gov. Updated April 1, 2024. Accessed November 30, 2024 ... csharp this parameterWebOct 29, 2024 · European Commission approves Zejula (niraparib) as first-line monotherapy maintenance treatment in advanced ovarian cancer . For media and investors only. ... The study was later amended to incorporate an individualised starting dose of either 200 mg or 300 mg of Zejula once-daily based on the patient’s baseline … c sharp this