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BioWorld - Thursday, March 5, 2026
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U.S. FDA headquarters

Industry cites need for audit of user fee financials in next user fee agreement

July 15, 2021
By Mark McCarty
Negotiations between the FDA and industry over the next device user fee are going on behind closed doors, but the agency’s summaries of these meetings suggest there are sharp disagreements. While the FDA continues to press industry on additional fees for the total product life cycle advisory program, industry’s dissatisfaction with the FDA’s fiscal management of the user fee program has prompted a demand for a one-off audit of the agency’s use of those user fees.
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Regulatory actions for July 15, 2021

July 15, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Istar Medical, Palliare.
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Dueling CMOs, Aduhelm takes it on the nose in CTAF session

July 15, 2021
By Randy Osborne
Members of the California Technology Assessment Forum (CTAF), an independent appraisal committee of the Institute for Clinical and Economic Review (ICER), discussed – and voted on – the safety vs. efficacy and other aspects of Biogen Inc.’s embattled Aduhelm (aducanumab), the amyloid beta-targeting therapy recently approved for Alzheimer’s disease. It didn’t go well for Biogen.
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Red pills spilling out of white bottle

Adcom says ‘not yet,’ but opens small window for roxadustat

July 15, 2021
By Mari Serebrov
Despite assembling the largest body of data the FDA said it may ever see for a drug intended to treat anemia due to chronic kidney disease, Fibrogen Inc. will have to get even more trial data to push roxadustat over the finish line in the U.S. – if the FDA follows the advice of its Cardiovascular and Renal Drugs Advisory Committee.
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Lepu’s NDA for anti-PD-1 antibody accepted ahead of Hong Kong IPO

July 15, 2021
By Doris Yu
The China NMPA’s Center for Drug Evaluation accepted Lepu Biopharma Co. Ltd.’s new drug application (NDA) for anti-PD-1 antibody candidate HX-008 (pucotenlimab). That comes after the company filed for an IPO in Hong Kong.
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FDA clamps down on ad claims impacting biosimilars

July 15, 2021
By Mari Serebrov
The FDA took Amgen Inc. to task for promotions claiming Neulasta (pegfilgrastim) Onpro on-body injector is more effective than pegfilgrastim delivered via a prefilled syringe.
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Regulatory actions for July 15, 2021

July 15, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alkeus, Antengene, Immunitybio, Kintor, Qualigen, Ryvu, Sesen.
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Regulatory actions for July 14, 2021

July 14, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Coaptech, Tidal Medical.
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Teva tests CREATES path in Amicus suit

July 14, 2021
By Mari Serebrov
Putting the 2019 CREATES Act to the test, Teva Pharmaceutical Industries Ltd. filed suit July 13 against Philadelphia-based Amicus Therapeutics Inc.
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Reichstag, German parliament building in Berlin

U.S. lawmakers pressure Germany on WTO IP waiver

July 14, 2021
By Mari Serebrov
Hoping to get Germany to drop its opposition to a proposed World Trade Organization (WTO) waiver of intellectual property (IP) rights, several U.S. lawmakers have asked to meet with German Chancellor Angela Merkel when she’s in Washington for a July 15 summit with President Joe Biden.
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