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BioWorld - Tuesday, January 27, 2026
Breaking News: BioWorld 2025 Year in ReviewBreaking News: BioWorld MedTech 2025 Year in ReviewBreaking News: Trump administration impacts continue to roil the life sciences sector
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Cost of using a priority review voucher going up, way up

Sep. 19, 2024
By Mari Serebrov
What comes down must go up seems to be the rule of thumb these days, even for U.S. FDA fees. The cost of using a priority review voucher (PRV) to shave four months off an FDA standard 10-month drug review has dropped drastically over the past several years. But come Oct. 1, biopharma companies will have to pay nearly 89% more than on the previous day to use a PRV.
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Laptop displaying FDA logo

US FDA issues CRL for Vanda’s tradipitant for gastroparesis

Sep. 19, 2024
By Karen Carey
Clearly frustrated by the U.S. FDA’s rejection of tradipitant to treat gastroparesis, Vanda Pharmaceuticals Inc. CEO Mihael Polymeropoulos said the agency is discouraging drug development for the serious gastric emptying condition for which there has been no new treatment in 40 years. The complete response letter (CRL) issued on the Sept. 18 PDUFA date for the neurokinin-1 receptor antagonist, which Vanda licensed from Eli Lilly and Co. in 2012, requested additional studies that the company said are not in line with the advice of experts in the field.
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Liver over digital lens background

Hark, Herald MASH phase II positive but Aligos THRown for a loop

Sep. 19, 2024
By Randy Osborne
After disclosing data from the phase II Herald study, Aligos Therapeutics Inc. may sign a partner to help advance ALG-055009, a thyroid hormone receptor (THR) beta agonist, in subjects with metabolic dysfunction-associated steatohepatitis (MASH, formerly nonalcoholic steatohepatitis, or NASH).
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Edgewise surges on early stage data

Sep. 19, 2024
By Lee Landenberger
Positive data from two studies boosted Edgewise Therapeutics Inc.’s market share and elevated analyst enthusiasm for the company and its treatment of obstructive hypertrophic cardiomyopathy. Top-line data from the phase I and phase II studies of EDG-7500 in treating the genetic disease that results in thickened heart muscles showed the therapy was well-tolerated in healthy volunteers and produced meaningful improvements in those with the disease.
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Financings for Sept. 19, 2024

Sep. 19, 2024
Biopharmas raising money in public or private financings, including: Altamira, Awakn, Brenus, Vaccinex.
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Other news to note for Sept. 19, 2024

Sep. 19, 2024
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Bavarian Nordic, Nanovation, Novo Nordisk, Nexilico, Pharmajet, Revive, Siolta, Scancell.
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Regulatory actions for Sept. 19, 2024

Sep. 19, 2024
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Accord, Applied, Astrazeneca, Azitra, Briacell, Glycomine, Imcheck, Merck, Moderna, Nicox, Novartis, Valneva.
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In the clinic for Sept. 19, 2024

Sep. 19, 2024
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Biomx, Biosyngen, BMS, GSK, Innovent, Insilico, Kyverna, TG Therapeutics.
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Appointments and advancements for Sept. 19, 2024

Sep. 19, 2024
New hires and promotions in the biopharma industry, including: Autolus, Cidara, Disc Medicine, Eyconis, Helsinn, Immix, Sernova.
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Brain waves
Neurology/psychiatric

ECTRIMS 2024: Time for neuroprotection

Sep. 19, 2024
By Coia Dulsat
The Annual Congress of the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) meeting in Copenhagen this week is celebrating its 40th edition. In recognition of this landmark, the plenary session and opening lecture were attended by Queen Margrethe of Denmark. Afterward, the hot topic session on neuroprotective therapies set the stage for the subsequent discussions on the latest trends in the management and treatment of multiple sclerosis (MS).
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