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BioWorld - Sunday, March 1, 2026
Home » Topics » Clinical

Clinical
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Man scratching arm

Skin-tight race in prurigo nodularis as Wall Street refracts Trevi’s PRISM data

June 29, 2022
By Randy Osborne
Trevi Therapeutics Inc. took its place among several late-stage contenders by scoring a win in prurigo nodularis in the form of positive data from the 360-participant, phase IIb/III Pruritus Relief through Itch-Scratch Modulation, or PRISM, trial with oral Haduvio (nalbuphine extended release).
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Clinical data illustration

Clinical reports slow in June as activity falls 15% behind 2021

June 28, 2022
By Karen Carey
Clinical data readouts in 2022 have fallen by 14.8% in comparison with the same timeframe last year, and more than half of all reports are for drugs and biologics targeting three major therapeutic areas. In the first six months of the year, there have been 1,707 clinical entries, compared with 2,004 last year.
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BIO 2022: Global trials face core challenges from privacy laws

June 28, 2022
By Michael Fitzhugh
As a growing roster of nations moves to protect individual genomic and other health data in the name of privacy under the General Data Protection Regulation in the EU and similar laws elsewhere, chief aggregators of such data, drug developers, are struggling.
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Young boy standing with walker

Italfarmaco’s givinostat hits phase III endpoint in DMD

June 27, 2022
By Cormac Sheridan
Italfarmaco SpA will seek meetings with the U.S. FDA and the European Medicines Agency to discuss filing requirements for givinostat in Duchenne muscular dystrophy (DMD) on the strength of data from a phase III trial in which those on the drug exhibited a slower decline in their ability to climb four stairs than those on placebo.
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BIO 2022: Global trials face core challenges from privacy laws

June 27, 2022
By Michael Fitzhugh
As a growing roster of nations moves to protect individual genomic and other health data in the name of privacy under the General Data Protection Regulation in the EU and similar laws elsewhere, chief aggregators of such data, drug developers, are struggling.
Read More

Sanofi-GSK’s beta-antigen COVID-19 vaccine posts strong numbers against omicron

June 24, 2022
By Lee Landenberger
Sanofi SA and GSK plc said new phase III data show their adjuvanted bivalent D614 and beta (B.1.351) COVID-19 vaccine candidate responded well against omicron despite it being designed to fight the original SARS-CoV-2 virus and the beta variant.
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Uniqure reassures with full-year low-dose data in HD; efficacy ahead with gene therapy?

June 23, 2022
By Randy Osborne
Uniqure NV rolled out stock-pleasing safety and biomarker data from 10 patients enrolled in the low-dose cohort of the ongoing phase I/II trial with AMT-130 for the treatment of Huntington’s disease (HD), but investors must wait for details on MRI scans. “We have communicated that we will discuss the MRI findings in the middle of next year,” CEO Matt Kapusta told investors during a conference call. “That’s all I can say.”
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06-22-workflow.png

New study signals potential of uniting AI and radiologists

June 22, 2022
By Catherine Longworth
A new large-scale study has found combining artificial intelligence (AI) and radiologists to analyze breast cancer screenings can lead to better patient outcomes, when compared with unaided radiologists and the use of AI alone. The study, published in The Lancet Digital Health, evaluated the performance of an AI decision referral system developed by Vara (MX Healthcare GmbH).
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Phase II fizzle in AD hammers Athira shares, unblinding of phase III mulled

June 22, 2022
By Randy Osborne
Shares of Athira Pharma Inc. (NASDAQ:ATHA) plunged almost 66.3%, or $5.60, to close at $2.85 on June 22 after the company disclosed top-line results from its exploratory phase II study with fosgonimeton (ATH-1017, fosgo) in mild-to-moderate Alzheimer’s disease (AD).
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Ionis, Astrazeneca target filing for amyloid-driven disease after phase III readout

June 21, 2022
By Michael Fitzhugh
Ionis Pharmaceuticals Inc. and Astrazeneca plc, partners on the antisense oligonucleotide inhibitor eplontersen, said interim phase III data showed the candidate had a positive impact on disease progression in patients with hereditary transthyretin-mediated amyloid polyneuropathy, giving them confidence to plan for a U.S. FDA NDA filing in the indication before the end of 2022.
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