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BioWorld - Saturday, June 21, 2025
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FDA Approved stamp

FDA grants accelerated approval for Padcev to treat urothelial cancer

Dec. 19, 2019
By Lee Landenberger
A mere 26 months after the first patient was enrolled in its pivotal phase II study and about three months ahead of its PDUFA date, the FDA granted accelerated approval for Padcev (enfortumab vedotin-ejfv) to treat adults with locally advanced or metastatic urothelial cancer who have previously received a PD-1/L1 inhibitor and a platinum-containing chemotherapy before (neoadjuvant) or after (adjuvant) surgery or in a locally advanced or metastatic setting.
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Regulatory front for Dec. 19, 2019

Dec. 19, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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Cancer cell

Taz-mania: Devil in details as Epizyme adcom votes ES yes 11-0 but wants more data

Dec. 18, 2019
By Randy Osborne
Though they made known their reservations about the patient sample size and queried front-line vs. second-line use of tazemetostat, members of the FDA’s Oncologic Drugs Advisory Committee (ODAC) voted 11-0 to recommend approval of the oral, first-in-class EZH2 inhibitor from Cambridge, Mass.-based Epizyme Inc.
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Regulatory front for Dec. 18, 2019

Dec. 18, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory front for Dec. 17, 2019

Dec. 17, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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Mirum, FDA meetings more than double the company’s stock value

Dec. 16, 2019
By Lee Landenberger
With two FDA meetings in its hip pocket to discuss maralixibat for treating pruritus associated with Alagille syndrome, Mirum Pharmaceuticals Inc. got a resounding boost from the market Monday as its stock (NASDAQ:MIRM) closed up 111%, at $17.28.
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FDA approves Amarin's Vascepa to reduce CV disease risk

Dec. 16, 2019
By Michael Fitzhugh
Little more than a month after the FDA's Endocrinologic and Metabolic Drugs Advisory Committee unanimously supported approval of Amarin Corp. plc's fish oil-based Vascepa (icosapent ethyl) for reducing the risk of cardiovascular (CV) events in adults with elevated triglyceride levels, the agency has greenlighted a label expansion for the already-approved medicine, allowing for its adjunctive use in that indication.
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Approved stamp

Qilu scores first Avastin biosimilar approval in China, set to drive down prices

Dec. 16, 2019
By Elise Mak
BEIJING – Jinan, China-based Qilu Pharmaceutical Co. Ltd. has won the first approval for a China-developed biosimilar to Avastin (bevacizumab, Roche Holding AG). Its biosimilar QL-1101, to be sold under the trade name Ankada, has been approved to treat advanced, metastatic or recurrent non-small-cell lung cancer and metastatic colorectal cancer.
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Regulatory front for Dec. 16, 2019

Dec. 16, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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FDA’s change of heart

Sarepta’s Vyondys 53 wins a surprise accelerated approval

Dec. 13, 2019
By Lee Landenberger
In August the FDA was skeptical about Sarepta Therapeutics Inc.’s injectable Vyondys 53 (golodirsen), but that changed swiftly Friday with the agency’s accelerated approval for the Duchenne muscular dystrophy (DMD) follow-on therapy, the first treatment specifically for this subtype.
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