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  • GSK buys a Winrevair rival for $950M & BreezeBio raises $60M for its gene-delivery technology

GSK buys a Winrevair rival for $950M & BreezeBio raises $60M for its gene-delivery technology

 

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Good morning! Remember when China was the discount rack for Western biotech pipelines? Not anymore. According to data from Evaluate, upfront payments in cross-border licensing deals have surged 230% since 2022, from $52M to $172M on average in 2026 so far. Deal count is up 120% and total upfront dollars up roughly 400% to $5.6B last year.

Why it matters: Chinese biotechs aren’t pricing like challengers anymore. With dominance in hot modalities – nearly half of clinical bispecifics, ADCs and CAR-T assets are from China – they have leverage and they’re using it to get upfront payments on par with what’s seen in the West. 

Bottom line: If you want to go shopping for cutting-edge assets in China, the bill just went up.

— Joachim E.

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SNAPSHOT

GSK breathes life into its pulmonary hypertension pipeline with a $950M bet on Winrevair rival

Walkarounds in Amsterdam.

GSK is acquiring Canadian biotech 35Pharma for $950 million in cash, gaining HS235, a phase 1-stage drug targeting the activin receptor pathway for pulmonary arterial hypertension (PAH) and related conditions.

Why it matters: PAH remains a serious, high-unmet-need disease, and Merck’s Winrevair generated $1.4 billion last year. If HS235 can match or outperform it, especially with fewer side effects, GSK could secure a major new growth driver.

Backstory: The deal marks GSK’s second biotech acquisition in two months under new CEO Luke Miels, who has prioritized “smart business development” to accelerate R&D. In January, GSK bought Rapt Therapeutics for $2.2 billion and its anti-IgE antibody. This week, it also agreed to pay $40 million for oligonucleotides from Frontier Biotechnologies.

Big picture: GSK is targeting assets that compete with existing blockbusters, but with differentiation. HS235 mirrors Merck’s Winrevair strategy, while Rapt’s antibody targets the same epitope as Novartis and Roche’s Xolair. The approach: improve on proven mechanisms to capture market share.

Zoom in: HS235 has completed a phase 1 trial in healthy volunteers and is preparing for patient studies in PAH and pulmonary hypertension linked to heart failure. Like Winrevair, it targets the activin receptor signaling pathway. It is engineered for enhanced selectivity to reduce binding to BMP9 and BMP10 ligands associated with bleeding and vascular side effects. Early data showed dose-dependent reductions in visceral fat, preservation or gains in lean mass, and sustained target engagement. GSK hopes the drug may also reduce bleeding risk, improve insulin sensitivity, and support weight management.

What’s next: HS235 will move into patient trials as GSK integrates the asset into its respiratory, immunology and inflammation portfolio. GSK´s CEO Luke Miels is implying even more pipeline expansion by signaling more deals ahead with an emphasis on accelerating R&D.

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SNIPPETS

What’s happening in biotech today?

💰 Series B: BreezeBio, formerly known as GenEdit, has raised $60 million in a Series B round to advance its shift from a gene-delivery technology platform to developing its own genetic medicines, focusing on autoimmune diseases and cancer. The South San Francisco-based company has spent a decade refining its “NanoGalaxy” polymer nanoparticle system, designed to precisely deliver genetic material to specific tissues and allow repeat dosing, attracting partnerships with companies such as Sarepta, Editas, and Genentech. Its lead program, BRZ-101, aims to induce immune tolerance in Type 1 diabetes and is entering final preclinical studies, while the new funding will also support expansion into in vivo cell therapies.

 💊 Oral biologics: Novo Nordisk has entered a collaboration with Boston-based startup Vivtex that could be worth up to $2.1 billion in milestone payments and royalties, giving Novo access to technologies aimed at improving the delivery of oral biologic drugs for obesity and other metabolic diseases. While financial details of the upfront payment were not disclosed, the deal supports Novo’s strategy of combining internal and external innovation to expand its cardiometabolic portfolio. Vivtex, founded in 2018, uses a “gut-on-a-chip” platform to test drug formulations for improved gastrointestinal absorption, positioning it as a key partner in advancing more convenient oral biologic therapies.

🤝 CTLA-4 deal: Harbour BioMed has entered a deal to out-license its clinical-stage anti-CTLA-4 antibody HBM4003 to newly formed Solstice Oncology in an agreement worth up to $1.1 billion in potential milestone payments and royalties outside Greater China. Harbour will receive $105 million upfront, including $50 million in cash, $5 million in near-term payments and over $50 million in equity in Solstice, which it co-founded and in which it will remain a shareholder. While the specific indication was not disclosed, the asset’s mechanism and Solstice’s name suggest a focus on oncology. Harbour, which specializes in immunology and oncology using its Harbour Mice platform, continues to pursue additional partnerships, including a recent deal with Bristol Myers Squibb.

 🛑 Trial hold: The FDA has imposed a partial clinical hold on MacroGenics’ phase 2 trial of lorigerlimab after serious adverse events, including thrombocytopenia, myocarditis and neutropenia, resulted in one patient’s death from septic shock. The company had already paused enrollment in the study, which is testing the PD-1/CTLA-4 bispecific antibody in platinum-resistant ovarian and clear cell gynecologic cancers, with 41 of approximately 60 planned patients enrolled. Those currently participating will continue treatment. MacroGenics intends to submit additional safety data and proposed protocol modifications to the FDA and aims to resolve the hold within the agency’s 30-day review window, marking another setback for the program following earlier safety challenges and discontinuations.

✂️ Gene editing: Pfizer has exercised its option to obtain global rights to an unnamed liver-targeted gene editing candidate from Beam Therapeutics, marking a renewed commitment to genetic medicines after exiting the gene therapy field last year. The decision stems from a four-year collaboration launched in 2021 that included a $300 million upfront payment and up to $1.05 billion in potential milestones. Pfizer will assume responsibility for development, manufacturing and commercialization, while Beam retains the option to co-develop and co-commercialize the asset after phase 1/2 trials. Separately, Beam secured a $500 million loan from Sixth Street to support the planned launch of its sickle cell therapy risto-cel and advance its in vivo pipeline.

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