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Home » Newsletters » BioWorld

BioWorld

Oct. 23, 2024

View Archived Issues
Handshake with DNA, molecules

Modifi acquired by Merck in $1.3B deal

Modifi Biosciences Inc. has come a long way very quickly. Spun out of Yale University in 2021, it published data on DNA in Science in July 2022, and now it’s being acquired by Merck & Co. Inc. for $30 million up front. Ultimately, Modifi shareholders could receive milestones of up to $1.3 billion. Read More

Alto’s ALTO-100 misses endpoints in phase IIb depression study

Despite positive findings from an earlier trial, Alto Neuroscience Inc.’s BDNF-targeting candidate, ALTO-100, failed to best placebo in a phase IIb study in major depressive disorder, sending shares of the company to their lowest price since going public in a February 2024 IPO, as investors worried about readthrough to Alto’s biomarker-based approach for treating psychiatric disorders. Read More
Green checkmark and red X

UK nod for Alzheimer’s drug Kisunla, but NICE says no coverage

The U.K. Medicines and Healthcare products Agency has become the third to approve Eli Lilly and Co.’s Kisunla (donanemab), but the drug’s spending watchdog has simultaneously ruled the Alzheimer’s disease treatment is not cost effective.

Read More

DBV making sure peanut-allergy patch plan sticks with FDA

DBV Technologies SA CEO Daniel Tasse said his firm will meet “very shortly” with the U.S. FDA for talks that will formalize an accelerated approval process for the Viaskin Peanut allergy patch. “Did this take longer than expected? Yes, it did,” Tasse said during a conference call update. “But this was a choice we made, and it was a necessary choice” in order to nail down precise requirements for the product. Read More
South-Korean-won1.png

Cellbion the latest radiopharma contender with Kosdaq IPO

Cellbion Co. Ltd. debuted on the tech-heavy Kosdaq board of the Korea Exchange Oct. 16, with share prices closing upward at ₩20,650 (US$14.94) – outdoing its initial price of ₩15,000 per share for 1.9 million shares. Read More

UK's MHRA eyes new regs for point-of-care drug manufacturing

The U.K.'s Medicines and Health Care Products Regulatory Agency (MHRA) has posted a series of draft new regulations that will increase the requirements for device makers doing business in the U.K. However, the agency has also floated a regulation for the production of pharmaceuticals at the point of care, a proposal MHRA said is the first of its kind. Read More

BioWorld Insider podcast: A quantum leap into the future of drug development

In the newest BioWorld Insider podcast, Victoria Lipinska, the America's lead for Quantum Innovation Centers at IBM Quantum, talks about the future of drug development using quantum computing. “The new technology is a completely different branch of computing as opposed to what we know right now, and it's meant to complement what we know, not to really replace it,” she said. Read More

Appointments and advancements for Oct. 23, 2024

New hires and promotions in the biopharma industry, including: Alphina, Apnimed, Arialys, Artiva, Disc Medicine, Flagship Pioneering, Kenai, Klotho, Ligachem. Read More

Financings for Oct. 23, 2024

Biopharmas raising money in public or private financings, including: Avencell, Biovie, Coya, GRI, Passkey, Scholar Rock, Septerna, Trellis. Read More

In the clinic for Oct. 23, 2024

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Annexon, Briacell, Clearside, Everest, Immunic, Minghui, Monopar, Oncternal, Otsuka, Quell. Read More

Other news to note for Oct. 23, 2024

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Bioversys, Editas, Genentech, Genevant, Grifols, Johnson & Johnson, Moderna, Nucleome, Rectify, Rhine Pharma, Telix, UCB, Zylem. Read More

Regulatory actions for Oct. 23, 2024

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alvotech, Camurus, Nido, Remedy, Sangamo, Teva. Read More

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