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BioWorld - Friday, January 16, 2026
Breaking News: BioWorld 2025 Year in ReviewBreaking News: BioWorld MedTech 2025 Year in ReviewBreaking News: Trump administration impacts continue to roil the life sciences sector
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Takeda moves mezagitamab to phase III in thrombocytopenia

June 24, 2024
By Tamra Sami
Takeda Pharmaceutical Co. Ltd. is progressing mezagitamab to phase III trials after the CD38 monoclonal antibody showed rapid and sustained increases in platelet counts in patients with persistent or chronic primary immune thrombocytopenia (ITP) in a phase IIb trial.
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Genentech’s Piasky cleared for paroxysmal nocturnal hemoglobinuria

June 24, 2024
By Karen Carey
Roche Holding AG’s Genentech Inc. unit received U.S. FDA approval on June 20 of Piasky (crovalimab) to treat adults and children 13 and older with paroxysmal nocturnal hemoglobinuria and a body weight of at least 40 kg (88 pounds).
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Breast cancer illustration

G1’s phase III misses in triple-negative breast cancer

June 24, 2024
By Lee Landenberger
Top-line phase III data from G1 Therapeutics Inc.’s pivotal Preserve 2 study of Cosela (trilaciclib) in treating metastatic triple-negative breast cancer missed its primary endpoint of overall survival, submerging the stock on June 24.
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‘Big win’ as Alnylam’s vutrisiran succeeds in rare heart disease

June 24, 2024
By Jennifer Boggs
Any skepticism that might have been lingering in the wake of Alnylam Pharmaceuticals Inc.’s February decision to tweak the analysis plan for the Helios-B trial testing vutrisiran in transthyretin amyloidosis with cardiomyopathy appeared to dissipate as the company reported top-line data showing the study met the primary and all secondary endpoints.
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Device patents still listed, FTC embraces chance to expand review

June 24, 2024
By Mari Serebrov
Even though the U.S. FTC recently claimed a court victory in its campaign to shut down the listing of device patents for drugs in the FDA’s Orange Book, 80% of the listings targeted in the commission’s first round of warning letters remain in place more than seven months later.
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Vyvgart Hytrulo

FDA approves Argenx's Vyvgart for rare autoimmune disease CIDP

June 24, 2024
By Randy Osborne
Argenx SE gained U.S. FDA approval of subcutaneously given Vyvgart Hytrulo (efgartigimod alfa and hyaluronidase-qvfc) for adult patients with chronic inflammatory demyelinating polyneuropathy (CIDP). The company’s stock (NASDAQ:ARGX) was up 11.7% to $440.59 at the close of trading June 24. About 24,000 people in the U.S. are being treated for CIDP, and patients are generally diagnosed between 40 and 60 years of age.
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Regulatory actions for June 24, 2024

June 24, 2024
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: BMS, Emergex, Janssen, Lexicon, Sarepta.
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Other news to note for June 24, 2024

June 24, 2024
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alivexis, Johnson & Johnson, Melodia, Proteologix.
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In the clinic for June 24, 2024

June 24, 2024
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Hightide, Ocugen, Sarton, Zealand.
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Financings for June 24, 2024

June 24, 2024
Biopharmas raising money in public or private financings, including: Ascentage, Avrobio, Palatin, Rakovina, Takeda, Tectonic.
Read More
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