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Two men die of exposure in Washington forest during trip to look for SasquatchTodd Greenberg, the current chief executive officer of the Australian Cricketers' Association, is set to succeed Nick Hockley as the new CEO of Cricket Australia (CA) this coming March, reports cricket.com.au. Greenberg's appointment follows Hockley, who served since 2020 after a turbulent era under Kevin Roberts. Greenberg is poised to become the 15th leader of Australian cricket's top governing body, which originated in 1892 as the Australasian Cricket Council. His cricketing background includes playing ten seasons for Randwick CC in Sydney as a top-order batter. He also gained considerable experience in sports administration, including managing the Mike Whitney School of Cricket. In a statement on cricket.com.au, Greenberg expressed his excitement, saying, "This is an exciting time for cricket with opportunities and challenges ahead. I'm keen to ensure the game continues to thrive nationwide." Greenberg's background includes a tenure as the National Rugby League's chief executive and a significant role in the ACA since January 2021, where he negotiated a Memorandum of Understanding for cricket. CA chair Mike Baird endorsed Greenberg, acknowledging his commercial acumen and innovative approach. "The recruitment panel and CA Board were impressed by Todd's passion for cricket and his vision for future growth," said Baird. He also extended gratitude to Hockley for leaving the game in a position of strength. (With inputs from agencies.)

Cabometyx is under clinical development by and currently in Phase II for Ureter Cancer. According to GlobalData, Phase II drugs for Ureter Cancer does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval. Cabometyx overview Cabozantinib s-malate (Cabometyx, Aptimetyx) is a s-malate salt form of cabozantinib, acts as an anti-neoplastic agent. It is formulated as film-coated tablets for oral route of administration. Cabometyx is indicated for the treatment of adult and pediatric patients 12 years of age and older with locally advanced or metastatic differentiated thyroid cancer (DTC) that has progressed following prior VEGFR-targeted therapy and who are radioactive iodine-refractory or ineligible. Cabometyx is indicated as monotherapy for the treatment of adult patients with locally advanced or metastatic differentiated thyroid carcinoma (DTC), refractory or not eligible to radioactive iodine (RAI) who have progressed during or after prior systemic therapy. Cabometxy is indicated for the treatment of advanced renal cell carcinoma (RCC) in treatment-naïve adults with intermediate or poor risk and in adult patients who have received prior therapy. Exelixis overview is a biopharmaceutical company that focuses on the development and commercialization of small molecule therapies for the treatment of cancer. The company’s marketed products include, Cometriq (cabozantinib), an inhibitor of multiple receptor tyrosine kinases; Cabometyx (cabozantinib) developed for the treatment of patients with advanced renal cell carcinoma (RCC), and hepatocellular carcinoma (HCC). The company’s major pipeline product candidates include zanzalintinib, XB002 and XL102 for the treatment of advanced or metastatic solid tumors, and CBX-12 for advanced metastatic refractory solid tumors. The company has collaborative partnerships with biopharmaceutical companies to advance the development of potential therapies for cancer and other serious diseases. is headquartered in Alameda, California, the US. For a complete picture of Cabometyx’s drug-specific PTSR and LoA scores, This content was updated on 12 April 2024 From Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors. , the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article. GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s .Israeli hospital says Netanyahu has undergone successful prostate surgery