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BioWorld - Wednesday, March 25, 2026
Home » Newsletters » BioWorld

BioWorld

April 15, 2024

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Stock chart, red down arrow

No early stop for status epilepticus phase III; Marinus falls

Investors anxious to see data from Marinus Pharmaceuticals Inc.’s phase III Raise study testing intravenous ganaxolone in refractory status epilepticus (RSE) will have to wait a little longer, as the trial failed to meet the predefined criteria for stopping at the interim analysis, sending shares (NASDAQ:MRNS) down nearly 83%. Read More

Ultragenyx’s Angelman prospect scores in phase I/II

Wall Street may not have responded as positively as Ultragenyx Pharmaceutical Inc. would have liked after the firm unveiled new data from the phase I/II study with GTX-102 for the treatment of Angelman syndrome (AS). Patients in expansion cohorts A & B treated with a set dose and regimen of the intrathecally delivered antisense oligonucleotide (ASO) showed rapid and clinically meaningful improvement across multiple domains. Read More
Coin stacks, dollar signs and up arrow

Biopharma follow-on boom makes 2024 a top year

The $27.9 billion raised through biopharma follow-on offerings in the early months of 2024 has hit industry records never seen before. So far in three-and-a-half months in 2024, the industry has raised more than was raised during 21 of the past 24 full years. Read More

Medicare proposes sizeable bump for sickle cell gene therapies

Some gene therapies could be big winners under the changes the U.S. Centers for Medicare & Medicaid Services (CMS) is proposing to Medicare’s new technology add-on program (NTAP) for its fiscal 2025 inpatient prospective payment system. Read More
pill over molecule structures

Preclinical convulsions in rabbits halt Neumora’s phase I

Preclinical data of rabbits having convulsions has prompted the U.S. FDA to place a clinical hold on Neumora Therapeutics Inc.’s phase I study of NMRA-266 in healthy adults. Neumora said about 30 participants had been dosed so far in the single ascending and multiple ascending dose study, with no evidence of convulsions seen. Read More

Rx trial innovation center opens at US FDA

To take clinical trial innovation to the next level, the U.S. FDA’s Center for Drug Evaluation and Research (CDER) is opening the CDER Center for Clinical Trial Innovation. The center, known as C3TI, “will be a central hub within CDER to support the implementation of innovative approaches to clinical trial design and conduct,” said Kevin Bugin, CDER’s lead for C3TI and deputy director of operations in the Office of New Drugs. Read More

ICYMI: Week in review, April 8-12, 2024

A quick look back at top stories. Read More

Biggest gainers and losers for April 8-12, 2024

The top 10 biopharma stock gainers and losers for the week. Read More

Financings for April 15, 2024

Biopharmas raising money in public or private financings, including: Endo, Longeveron, Oncocyte, Renovrx, VBI Vaccines. Read More

In the clinic for April 15, 2024

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Abbvie, Agenus, Marius, Ocuphire, Sparx, Theracosbio, Transthera. Read More

Other news to note for April 15, 2024

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Hope Therapeutics, Nrx, Nephron, Paxmedica, Portage. Read More

Regulatory actions for April 15, 2024

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Oncolytics Biotech. Read More

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