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BioWorld - Monday, March 2, 2026
Home » Newsletters » BioWorld

BioWorld

Sep. 19, 2024

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

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). Read More

Edgewise surges on early stage data

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. Read More
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US FDA issues CRL for Vanda’s tradipitant for gastroparesis

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. Read More

Cost of using a priority review voucher going up, way up

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. Read More
brain neurological

ECTRIMS 2024: Time for neuroprotection

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). Read More

Astellas patent survives ‘natural law’ decision

The U.S. Court of Appeals for the Federal Circuit reined in a district court that invalidated three claims in an Astellas Pharma Inc. patent protecting bladder drug Myrbetriq (mirabegron) based on a issue that was never argued. Read More

Appointments and advancements for Sept. 19, 2024

New hires and promotions in the biopharma industry, including: Autolus, Cidara, Disc Medicine, Eyconis, Helsinn, Immix, Sernova. Read More

Financings for Sept. 19, 2024

Biopharmas raising money in public or private financings, including: Altamira, Awakn, Brenus, Vaccinex. Read More

In the clinic for Sept. 19, 2024

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Biomx, Biosyngen, BMS, GSK, Innovent, Insilico, Kyverna, TG Therapeutics. Read More

Other news to note for Sept. 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. Read More

Regulatory actions for Sept. 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. Read More

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