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BioWorld - Monday, June 8, 2026
Home » Newsletters » BioWorld

BioWorld

May 20, 2026

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Hands highlighted with joint pain

Immunovant rises on IMVT-1402 data in difficult-to-treat RA

Shares of Immunovant Inc. (NASDAQ:IMVT) gained 35% after the firm disclosed early but “compelling” data from a phase IIb study testing next-generation FcRn inhibitor IMVT-1402 in patients with difficult-to-treat rheumatoid arthritis (D2T RA), including those whose disease has persisted despite treatment with TNF and JAK inhibitors. Read More
Biosensors International Allegra transcatheter heart valve

All Women data show Allegra edge in female TAVR patients

Data from the All Women clinical trial, which looked at the Allegra transcatheter aortic valve replacement (TAVR) system compared to balloon-expandable valves (BEV) in women with aortic stenosis, showed that Allegra delivered lower mean gradients and less prosthesis-patient mismatch than BEVs. The data presented at the EuroPCR conference in Paris was the first randomized head-to-head comparison of different TAVR platforms conducted exclusively in women. Read More
Chinese flag and microscopes

Hengrui, BMS deal watershed moment for China biotech

The recent multibillion-dollar licensing alliance between Bristol Myers Squibb Co. and Jiangsu Hengrui Pharmaceuticals Co. Ltd is not an outlier, but rather the clearest sign yet that China’s biotech industry has entered a new phase of global influence. Read More
Guardant360 Liquid cDx

FDA approval advances personalized cancer diagnostics

The evolution of cancer diagnostics continues with the FDA’s May 20 approval of Guardant Health Inc.’s Guardant360 Liquid cDx. The new blood-based comprehensive genomic test assesses a 100-times wider genomic footprint than the previously approved Guardant360 cDx to deliver comprehensive tumor profiling results, according to the company. It noted that the seven companion diagnostic indications already approved for the older test will transfer to the new one. Read More
WHO response to Ebola outbreak in DRC

Sizing up an epidemic, with diagnostics and bioinformatics

It is not surprising that a large Ebola outbreak would be considered a public health emergency of international concern. But the current PHEIC is notable for the speed with which it was declared, speaking to the urgency of the situation. World Health Organization Director-General Tedros Adhanom Ghebreyesus declared the outbreak a PHEIC on Sunday, May 17, without first convening an emergency committee. That step is unprecedented.

Read More
Boston Scientific Watchman FLX

Subgroup analysis of the Champion-AF trial shows age not a factor

A subgroup analysis of data from Boston Scientific Corp.’s Champion-AF trial, which looked at the outcomes for patients with atrial fibrillation treated with a left atrial appendage closure (LAAC) device compared to direct oral anticoagulants (DOACs), found that the efficacy and safety of LAAC compared to DOAC are not affected by age. The data were presented at the EuroPCR conference in Paris. Read More

US Fed Circuit clarifies standing in the face of licensures

The short story of the U.S. Court of Appeals for the Federal Circuit’s May 19 opinion in Recor Medical Inc. v. Medtronic Ireland is that the lower court got it wrong when it ruled Medtronic lacked the required standing to bring an infringement countersuit against Recor because it had granted an exclusive license for products covered by the two asserted patents. The case was reversed and remanded. Read More

SEC settlements to take on a new look going forward

As of May 21, the U.S. SEC’s “no-deny” settlement policy is dead. For the past 50 years, the agency has required settling defendants to sign an agreement stating that they neither admit nor deny the SEC’s allegations. And beyond that, the standard settlement prohibits, under threat of court action, the defendants from ever denying the allegations publicly. According to an SEC notice to be published in the May 21 Federal Register, the agency has reconsidered the issue and is now rescinding the no-deny rule. Read More
Acid alpha-glucosidase molecular structure isolated on black

‘Detargeted’ targeted gene therapy improves activity in Pompe

A new strategy aims to improve gene therapy for Pompe disease by optimizing both the genetic component that restores the function of a deficient lysosomal enzyme and the vector that delivers it to the target tissue while avoiding the liver. The findings suggest that combining an optimized transgene with a targeted capsid could significantly enhance the effectiveness of gene therapy for Pompe disease. Read More

Appointments and advancements for May 20, 2026

New hires and promotions in the biopharma and med-tech industries, including: Anaveon, Arbor, Artiva, ATB, Atrandi, Azafaros, Cosette, Glutronics, Hephaistos, IDL Diagnostics, Immunic, Ladder, Lifeward, Okyo, Passkey, Ultima, Vistagen. Read More

Financings for May 20, 2026

Biopharma and med-tech companies raising money in public or private financings, including: Accro, Brainstorm, Forlong, Full-Life, Lauxera Capital, Nanoviricides, Sunshine, Tarsier, Violet, Vortex. Read More

In the clinic for May 20, 2026

Clinical updates for biopharma and med tech, including data readouts and publications: Boston Scientific, Elixir, Immunitybio, Mabylon, Nexgel, Oligomerix, Relay, Sanofi, Savara, Sensome, Sustained, Tiziana, United, Upstream, Upstream, Vast, Wave, Zena. Read More

Other news to note for May 20, 2026

Biopharma and med-tech happenings, including deals and partnerships, and other news in brief: Edison, Exelixis, Hansa, Helio, Herantis, Incyte, Indivi, Inmed, Mentari, Merck, Neurocrine, Nexalin, Novo Nordisk, One Biosciences, Ponm, Serb, Syneos, Verici Dx. Read More

Regulatory actions for May 20, 2026

Regulatory snapshots for biopharma and med tech, including global submissions and approvals, and other regulatory decisions and designations: Astrazeneca, Bayer, Belite Bio, Cullinan, Intrabio, Lupin, Galvanize, Portal Access, Sunrise. Read More

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