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BioWorld - Saturday, January 3, 2026
Home » Topics » Clinical

Clinical
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Henley Ion Virus Defender device

New Orleans device firm reveals high hopes for COVID defense tech

Jan. 14, 2022
By Catherine Longworth
Henley Ion Inc. is encouraged by early testing of a COVID-19 protection device. Henley’s Ion Virus Defender technology uses micronized electrostatic precipitation (mEP) to remove infectious bioaerosols from both inhaled and exhaled air. The company said initial tests of the prototype removed 99.8% of SARS-CoV-2 bioaerosols under Biosafety Level 3 testing conditions.
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Australia gears up for clinical trials with psychedelics to treat mental health disorders

Jan. 14, 2022
By Tamra Sami
PERTH, Australia – Australia has recently established new research and discovery centers to study psychedelic treatments for mental health disorders. Headquartered Melbourne, the Psychae Institute is a global research collaboration supported by a AU$40 million (US$29 million) investment from a North American biotechnology company.
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Surveying VEGF+DLL4 bids: Compass pointed in favorable direction

Jan. 14, 2022
By Randy Osborne
Targeting VEGF and DLL4 at the same time in solid tumors is an approach that continues to entice researchers, with such firms as Abbvie Inc., Compass Therapeutics Inc. and Oncxerna Therapeutics Inc. working to come up with oncology solutions.
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Panel: Aduhelm win benefits AD space despite noise and hurdles

Jan. 11, 2022
By Randy Osborne
“There isn’t a better place to be” now than in Alzheimer’s disease (AD) drug development, said Phyllis Ferrell, global head of external engagement in AD and neurodegeneration at Eli Lilly and Co., during Biotech Showcase’s panel talk titled, “Aduhelm: Stimulating the Next Generation of AD Treatment.”
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Durable goods? Biomarin ‘rox’ in hemophilia A with two-year gene therapy data

Jan. 10, 2022
By Randy Osborne
Having unveiled more data from the ongoing, global phase III Gener8-1 study with Roctavian (valoctocogene roxaparvovec, also known as valrox), Biomarin Pharmaceutical Inc. remains on track to file a regulatory submission with the FDA in the second quarter of this year for the gene therapy to treat adults with severe hemophilia A. The EMA is already reviewing a marketing authorization application.
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Woman sleeping

Scheduling conflict? Harmony’s Wakix, not bound by DEA, targets Xywav share in IH

Jan. 7, 2022
By Randy Osborne
Harmony Biosciences Holdings Inc.’s plan disclosed at the start of last December to launch a phase III study with Wakix (pitolisant) for idiopathic hypersomnia (IH) during the first half of this year brought renewed attention to the sleep space, where a handful of players are jostling for position.
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Lupus, pneumonitis mar Annexon phase II data with C1q blocker in HD

Jan. 5, 2022
By Randy Osborne
Annexon Inc. deemed promising – as did analysts – the interim phase II data with C1q protein complex inhibitor ANX-005 in Huntington’s disease (HD), but the safety profile took Wall Street aback, and shares (NASDAQ:ANNX) sank $3.75, or 34%, to close at $7.26.
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Stentrode device

Synchron brain-computer interface enables first thought-to-tweet

Jan. 4, 2022
By Annette Boyle
Synchron Inc. closed out 2021 by providing an opening for a patient with amyotrophic lateral sclerosis (ALS) to send the first thought transferred to a tweet via an implantable brain computer interface. Philip O’Keefe, who received one of the company’s Stentrode implants in April 2020, took over the Twitter account of Sychron CEO Thomas Oxley to say, “Hello, World. Short tweet. Monumental progress.”
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Avrobio shares sink as Fabry trial results weigh on prospects

Jan. 4, 2022
By Michael Fitzhugh
Avrobio Inc., stung by variable outcomes in a phase II test of its investigational Fabry disease therapy, is quitting further enrollment in the program, one of the first from its gene therapy platform, Plato. The team's attention will shift instead to other clinical-stage lysosomal disorder programs amid "an increasingly challenging market and regulatory environment for Fabry disease," the company said.
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Coronavirus vaccine illustration

J&J’s COVID-19 vaccine flexes its muscle against Omicron

Dec. 30, 2021
By Lee Landenberger
Preliminary data from a phase IIIb study of Johnson & Johnson’s Ad26.COV2.S COVID-19 vaccine showed a homologous booster dose was 85% effective against hospitalization in participants from South Africa.
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