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BioWorld - Sunday, July 19, 2026
Home » Topics » Respiratory, BioWorld

Respiratory, BioWorld
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Henlius lands European approval of PD-1 lung cancer drug

Feb. 6, 2025
By Marian (YoonJee) Chu
The European Commission on Feb. 5 cleared Shanghai Henlius Biotech Inc.’s serplulimab (HLX-02) under the brand name of Hetronifly as a first-line combination therapy with carboplatin and etoposide to treat extensive-stage small-cell lung cancer.
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Photo of bird, H5N1 virus
Infection

Antibody prevents severe bird flu in macaques

Feb. 3, 2025
By Mar de Miguel
Scientists at the University of Pittsburgh have tested a broadly neutralizing antibody that binds the stem of a protein against H5N1 avian influenza, which prevented severe disease in nonhuman primates and was effective for at least 8 weeks. The scientists remark on the potential of the design developed by Astrazeneca plc against a possible outbreak of the influenza A virus.
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Windward Bio launches with an in-licensed asset for asthma and COPD

Jan. 10, 2025
By Brian Orelli
Windward Bio AG was established with plans to both license a drug and establish wet labs to create an internal pipeline of drug candidates. SR One, Omega Funds, RTW Investments, Qiming Venture Partners, Quan Capital and Pivotal Bioventure Partners funded the Basel, Switzerland-based company’s $200 million series A financing round.
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Yuhan, Oscotec stock gains as J&J hits ‘gold standard’ in NSCLC

Jan. 8, 2025
By Marian (YoonJee) Chu
Yuhan Corp., Oscotec Inc. and Genosco Inc. were three companies with Asian ties to reap benefit from Johnson & Johnson’s stellar top-line Mariposa study results, wherein J&J’s Rybrevant (amivantamab-vmjw) and Lazcluze (lazertinib) combo regimen beat out Astrazeneca plc’s standard of care in non-small-cell lung cancer (NSCLC).
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Photo of Jaeyong Ahn and Jean-Francois Toussant in signing ceremony

Sanofi expands SK Bio deal, starts phase III of GBP-410

Dec. 23, 2024
By Marian (YoonJee) Chu
SK Bioscience Co. Ltd. won €50 million (₩75.5 billion, US$52.03 million) up front from Sanofi SA to expand an earlier agreement to develop and commercialize novel pneumococcal conjugate vaccines (PCVs). The first deal resulted in GBP-410 (SP-0202), its pediatric 21-valent PCV candidate that moved into phase III study last week.
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Alyftrek specs check out in cystic fibrosis as Vertex wins FDA nod

Dec. 23, 2024
By Randy Osborne
Vertex Pharmaceuticals Inc.’s chief operating officer Stuart Arbuckle said during the Stifel Healthcare Conference in November that his firm’s launch last year of Casgevy (exagamglogene autotemcel) for sickle cell disease and transfusion-dependent beta-thalassemia “was the beginning of diversifying on top of our cystic fibrosis [CF] base” – a base that itself continues to grow.
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Kyorin in-licenses Bayer’s phase II sleep apnea drug for €85M+

Dec. 17, 2024
By Tamra Sami
Kyorin Pharmaceutical Co. Ltd. has acquired Bayer AG’s phase II obstructive sleep apnea candidate, BAY-2925976, in a deal worth €85M (US$89.3 million) plus sales-based royalties and commercial milestones.
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Puretech’s modified pirfenidone impresses in phase IIb IPF trial

Dec. 16, 2024
By Nuala Moran
Puretech Health plc has announced phase IIb data showing its reformulation of pirfenidone has improved the tolerability and increased the efficacy of the marketed antifibrotic in the treatment of idiopathic pulmonary fibrosis. The tweak on the original molecule involved substituting three hydrogen atoms with three of the heavier counterpart, deuterium, improving stability, whilst retaining the antifibrotic effect.
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GC Biopharma to buy Abo Holdings for ₩138B, grow US plasma biz

Dec. 13, 2024
By Marian (YoonJee) Chu
GC Biopharma Corp. will buy plasma collector Abo Holdings Inc. in a ₩138 billion (US$96.28 million) cash acquisition as the vaccine and plasma-derived medicinal products developer works to accelerate entry of Alyglo (IVIG-SN 10%) in the U.S., where it was approved last year.
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Lungs

Trial’d on for size, Trevi’s Haduvio fits nice in IPF cough

Dec. 12, 2024
By Randy Osborne
News that Trevi Therapeutics Inc. got the size just right of the phase IIb Coral trial with Haduvio (oral nalbuphine extended release) led the company’s shares (NASDAQ:TRVI) to close Dec. 12 at $3.60, up $1.11, or 45%, after trading as high as $4.60.
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