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United States · United StatesFDA clears expanded use of AKEEGA as the first PARP-based precision combo for BRCA2-mutated mCSPC, cutting progression or death 54 percent and delaying symptoms 59 percent in Phase 3.See the Story
Johnson & Johnson (NYSE: JNJ) Gets FDA OK; AKEEGA Delays BRCA2 mCSPC Progress 59 Percent
61% Center coverage: 36 sources

Dublin, Ireland · DublinDUBLIN, Dec. 9, 2025 /PRNewswire/ -- ProVerum Limited, a medical device company focused on innovative, safe and effective solutions for treating benign prostatic hyperplasia (BPH), today announced it has received FDA approval for its ProVee® System for BPH.See the Story
FDA Approves the ProVee System - the First of a New Generation of Prostatic Urethral Stents for Treatment of BPH
58% Center coverage: 12 sources
