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Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Too bad for Tookad: FDA adcom votes against Steba’s prostate cancer treatment

Feb. 26, 2020
By Lee Landenberger
Citing what it called poor study design and execution coupled with a lack of follow-up data, the FDA’s Oncologic Drugs Advisory Committee voted 13-2 against recommending approval of Steba Biotech SA’s NDA for Tookad (padeliporfin dipotassium) for injection in men with localized early stage prostate cancer.
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Architectural pillars

Judge orders HHS to fill 10-year data gap on Clinicaltrials.gov

Feb. 26, 2020
By Mari Serebrov
While the staff at the U.S. Department of Health and Human Services (HHS) is currently all hands-on-deck in responding to the COVID-19 outbreak, some of the agencies in the department may have to divert resources to get sponsors of drug and device clinical trials to fill in nearly a decade-long data gap on Clinicaltrials.gov. That’s if a judge’s decision handed down this week stands.
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Regulatory front for Feb. 25, 2020

Feb. 25, 2020

The latest global regulatory news, changes and updates affecting biopharma, including: Actavis, Horizon, Yibin Lihao.


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Brain illustration

Lundbeck’s newly approved Vyepti enters a growth market for migraine prevention

Feb. 24, 2020
By Lee Landenberger
H. Lundbeck A/S’ antibody-based migraine therapy, Vyepti (eptinezumab-jjmr), which just received FDA approval as the first and only intravenous preventive treatment for adults, enters a market forecast to grow to $7 billion by 2027. While some analysts placed Vyepti’s earnings potential at about $800 million annually, the drug itself is positioned to become a possible blockbuster, earning $1 billion annually.
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Regulatory front for Feb. 24, 2020

Feb. 24, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Eastgate, Lilly, Pixarbio, Steba.
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Blood sample, DNA

Biomarin’s BLA for Valrox gene therapy for hemophilia A accepted by FDA

Feb. 24, 2020
By Peter Winter
Valrox (valoctocogene roxaparvovec) from San Rafael Calif-based Biomarin Pharmaceutical Inc. moved one step closer to entering the U.S. market, with the company reporting that that the FDA had accepted for priority review the BLA for its investigational AAV5 gene therapy for adults with hemophilia A.
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Esperion wins FDA approval for new cholesterol-lowering drug

Feb. 21, 2020
By Michael Fitzhugh
Less than a month after landing a positive opinion from the EMA's CHMP, Esperion Therapeutics Inc. has won FDA approval for bempedoic acid as an adjunct to diet and maximally tolerated statin therapy.
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FDA Approved road sign

Angle of ketorolac attack yakked as Baudax hails Anjeso pesos

Feb. 21, 2020
By Randy Osborne
During a conference call with investors, Baudax Bio Inc. CEO Gerri Henwood let out an exuberant “woohoo!” to celebrate the FDA’s approval – after two turndowns and much haggling over data – of Anjeso (meloxicam) for moderate to severe pain. Echoing her sentiment was Piper Sandler analyst David Amsellem. “It’s nice to see the pain division finally get this one right,” he said.
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Regulatory front for Feb. 21, 2020

Feb. 21, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Ferring Pharmaceuticals.
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Biosimilar drugs

FDA prepares for NDA-to-BLA deeming day

Feb. 20, 2020
By Mari Serebrov
With deeming day a little more than a month away, the FDA is taking final steps to ease the transition of simple proteins approved as new drug applications (NDAs) to biologic license applications (BLAs). The March 23 change will open drugs such as insulin and various hormones to new competition, likely bringing in the next wave of biosimilars. And this time, interchangeability could be riding the crest.
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