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BioWorld - Sunday, July 12, 2026
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Meeting illustration

Tsunami of change to challenge PDUFA VII

July 23, 2020
By Mari Serebrov
Although PDUFA VI still has two years of life left to it, PDUFA VII is already in the birthing process, with the use of real-world data (RWD), AI, and a coming surge of novel cell and gene therapies looking to be prominent features of the next five-year user fee agreement. Politics likely will play a role as well.
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FDA lifts Cymabay’s clinical holds while Genfit struggles

July 23, 2020
By Lee Landenberger
The FDA has lifted all the clinical holds it placed on seladelpar from Cymabay Therapeutics Inc. for INDs in nonalcoholic steatohepatitis (NASH), primary biliary cholangitis (PBC) and primary sclerosing cholangitis, giving the company new hope.
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Regulatory front for July 23, 2020

July 23, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Arbutus, Moderna.
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Regulatory actions for July 23, 2020

July 23, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Adial, Cymabay, Elsalys, Inotrem, Milestone, Neumentum, Vita.
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Cybersecurity data lock

Culture of scientific exchange seen as a risk factor for life science cybersecurity

July 22, 2020
By Mark McCarty
The U.S. government has charged two citizens of China with cybercrime in connection with purported hacking of research into vaccines for the SARS-CoV-2 virus, but more than one speaker on a July 22 webinar said scientists involved in basic life science research at universities fail to appreciate the need for cybersecurity, a problem they may take with them to the private sector.
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Green traffic light

Micro-X gets FDA green light for Rover mobile X-ray for military medical use

July 22, 2020
By Tamra Sami
PERTH, Australia – The U.S. FDA gave the thumbs up to Australia’s Micro-X Ltd. for its Rover mobile X-ray system. The 510(k) application was cleared in just five weeks. The concept for the Rover was originally developed under a contract with the Australian Department of Defense to prove that Micro-X’s technology could fulfill an unmet need for a full performance, digital medical X-ray imager that was light enough to be used in deployed medical facilities.
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Regulatory front for July 22, 2020

July 22, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Cordant, MITA.
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Regulatory actions for July 22, 2020

July 22, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Becton Dickinson, Canon Medical, Cerapedics, Integra, X-Nav Technologies.
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Wake-up call: FDA approves excessive daytime sleepiness treatment from Jazz

July 22, 2020
By Lee Landenberger
The FDA has approved Xywav (calcium, magnesium, potassium and sodium oxybates; JZP-258), an oxybate product for treating both cataplexy and excessive daytime sleepiness in narcolepsy patients ages 7 and older, from Jazz Pharmaceuticals plc.
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Technical difficulties illustration

Virtual meetings bring new challenges to adcoms

July 22, 2020
By Mari Serebrov
Interludes of classical music. Little kids talking in the background. Unmuted mics as panelists multitask. Gurgles of “underwater” sound. Periods of silence as speakers forget to unmute. And then the technical problems – lots of them. Such are the challenges of addressing a virtual FDA advisory committee in the time of COVID-19.  
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