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BioWorld - Friday, April 10, 2026
Home » Topics » Drugs » Protein

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Woman taking Amsler grid eye exam

Innovent’s IBI-302 meets phase III endpoints in neovascular AMD

March 31, 2026
By Tamra Sami
No Comments
Innovent Biologics Inc.’s efdamrofusp alfa (IBI-302) met the primary endpoint in the phase III Star trial in neovascular age-related macular degeneration (nAMD), and the Suzhou, China-based company will submit an NDA to China’s National Medical Products Administration.
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Anktiva

Unapproved Anktiva claims earn Immunitybio FDA warning

March 25, 2026
By Mari Serebrov
No Comments
Repeated promotional claims Patrick Soon-Shiong made about Immunitybio Inc.’s Anktiva – such as “We have now discovered and developed this drug … approved for bladder cancer, but it actually can treat all cancers” – landed the Culver City, Calif., company a strongly worded warning letter from the U.S. FDA.
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Woman taking Amsler grid eye exam

Innovent’s IBI-302 meets phase III endpoints in neovascular AMD

March 25, 2026
By Tamra Sami
No Comments
Innovent Biologics Inc.’s efdamrofusp alfa (IBI-302) met the primary endpoint in the phase III Star trial in neovascular age-related macular degeneration (nAMD), and the Suzhou, China-based company will submit an NDA to China’s National Medical Products Administration.
Read More
Stock market crash illustration

Immutep stock plummets 90% on efti phase III failure in NSCLC

March 17, 2026
By Tamra Sami
No Comments
Immutep Ltd.’s stock on Australia’s Securities Exchange plummeted nearly 90% on March 13 on the news that its phase III TACTI-004 trial evaluating eftilagimod alfa (IMP-321, efti) in first-line non-small-cell lung cancer was discontinued due to futility.
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Stock market crash illustration

Immutep stock plummets 90% on efti phase III failure in NSCLC

March 13, 2026
By Tamra Sami
No Comments
Immutep Ltd.’s stock on Australia’s Securities Exchange plummeted nearly 90% on March 13 on the news that its phase III TACTI-004 trial evaluating eftilagimod alfa (IMP-321, efti) in first-line non-small-cell lung cancer was discontinued due to futility.
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Kidneys

Vertex filing BLA for ‘best-in-class’ IgAN drug on Rainier win

March 10, 2026
By Karen Carey
No Comments
Vertex Pharmaceuticals Inc. is on track to complete a BLA by the end of March seeking potential U.S. accelerated approval for povetacicept, its dual inhibitor of the BAFF and APRIL cytokines, to treat immunoglobulin A nephropathy (IgAN), following a successful phase III Rainier trial.
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Lungs, heart anatomy

Returning to pulmonary hypertension, GSK buys 35Pharma

March 3, 2026
By Marian (YoonJee) Chu
No Comments
GSK plc is paying $950 million cash to acquire 100% of 35Pharma Inc.’s equity and pipeline, including phase II-ready candidate HS-235 for pulmonary hypertension. The acquisition agreement comes a day after GSK added two small interfering RNA assets from Nanjing, China-based Frontier Biotechnologies Inc. through a license deal reaching up to $1 billion.
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Ninth Circuit agrees with Lilly in royalty dispute

Feb. 26, 2026
By Mari Serebrov
No Comments
Eli Lilly and Co. got a breather when the U.S. Ninth Circuit Court of Appeals agreed that the company doesn’t owe Research Corporation Technologies Inc. (RCT) royalties on its diabetes drugs under a licensing agreement Lilly had made with Phillips Petroleum Co. in 1990 and that Phillips later sold to RCT.
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GI-ORIS-pic-Vivtex-2-25.jpg

Vivtex’s oral drug delivery approach draws Novo in $2.1B deal

Feb. 25, 2026
By Jennifer Boggs
No Comments
Coming off a U.S. FDA approval of the first GLP-1 in pill format, Novo Nordisk A/S leaned further into oral drug delivery efforts, partnering with Vivtex Corp. to develop next-generation oral formulations of peptide and protein therapeutics in a potential $2.1 billion deal that marks the highest-profile news for Vivtex since the firm spun out of MIT in 2018.
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Lungs, heart anatomy

Returning to pulmonary hypertension, GSK buys 35Pharma

Feb. 25, 2026
By Marian (YoonJee) Chu
No Comments
GSK plc is paying $950 million cash to acquire 100% of 35Pharma Inc.’s equity and pipeline, including phase II-ready candidate HS-235 for pulmonary hypertension. The acquisition agreement comes a day after GSK added two small interfering RNA assets from Nanjing, China-based Frontier Biotechnologies Inc. through a license deal reaching up to $1 billion.
Read More
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