
Articles
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1 day ago |
fiercebiotech.com | James Waldron
Invivyd has touted its follow-up to the FDA-authorized monoclonal antibody Pemgarda as potentially offering better protection against COVID-19 than available vaccines. Pemgarda received emergency use authorization from the FDA last year for pre-exposure prophylaxis of COVID-19 in certain adults and adolescents with moderate-to-severe immune compromise.
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2 days ago |
fiercebiotech.com | James Waldron
Altimmune’s GLP-1/glucagon dual receptor agonist achieved a hit and a miss when it came to the dual goals of a phase 2 metabolic dysfunction-associated steatohepatitis (MASH) study, while still showcasing the asset’s weight loss potential. Investors appeared disheartened by the results, sending Altimmune’s stock down 59% to $3.18 in pre-market trading Thursday from a Wednesday closing price of $7.71.
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2 days ago |
fiercebiotech.com | James Waldron
Hummingbird Biosciences could one day feather its nest with up to $290 million if its decision to license a phase 2-ready cancer drug to Percheron Therapeutics pays off. In return for up to $290 million in upfront and potential milestone payments—Hummingbird didn’t offer a breakdown of the financial details—Percheron has received the license to HMBD-002, an anti-VISTA monoclonal antibody designed to inhibit tumor growth.
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3 days ago |
fiercebiotech.com | James Waldron
Arbutus Biopharma had made no secret of its plans to step up its work on imdusiran. Now, the company has regained the China rights to the potential functional cure for hepatitis B. China-based Qilu Pharmaceutical secured the regional rights to imdusiran, then known as AB-729, back in 2021 for a $40 million upfront fee. If Arbutus had stuck with the deal, it could have been in line for up to $245 million in development, regulatory and sales milestones payments.
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3 days ago |
fiercebiotech.com | James Waldron
Biogen has pointed to an early readout from a small phase 1 trial as evidence that its antisense oligonucleotide salanersen could help children with spinal muscular atrophy (SMA) who are still struggling to sit independently despite having received Novartis’ Zolgensma.
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Interesting to hear GSK CEO Emma Walmsley say that Big Pharma should "run towards" conversations about vaccine efficacy as the new U.S. admin approaches. My initial writeup of the #JPM2025 session is here... https://t.co/ir4daAfdFx

For this week's @FierceBiotech podcast, I caught up with @novonordisk's Marcus Schindler to talk about the future of GLP-1s and the lessons he's learned as Chief Scientific Officer https://t.co/82yunwgPuE

My dispatch from Day 1 of Jefferies 2024 - where everyone is now making the comparison with JPM (including the bad weather)

Jefferies London Healthcare Conference, which until last year had been a relatively cozy affair, has seemingly become a victim of its own success. Is the meeting the next JPM? https://t.co/Z1FVDYQX4e