Category Press Releases

ImmunoPrecise Antibodies (IPA) Announces Q1 Fiscal 2025 Financial Results and Key Business Highlights

ImmunoPrecise Antibodies Ltd. (NASDAQ: IPA), an AI-driven biotherapeutics research and technology company, has announced its financial results for the first quarter of fiscal 2025, ending on July 31, 2024. All figures are reported in Canadian dollars (CAD) unless stated otherwise.…

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Japan Approves CSL and Arcturus’ Updated mRNA COVID-19 Vaccine for JN.1 Strain

Global biotechnology leader CSL (ASX:CSL; USOTC:CSLLY) and sa-mRNA pioneer Arcturus Therapeutics have announced that Japan’s Ministry of Health, Labor and Welfare (MHLW) has approved their updated self-amplifying mRNA (sa-mRNA) COVID-19 vaccine, KOSTAIVE®. This vaccine is designed to protect adults 18…

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Sanofi, RadioMedix, and Orano Med Sign Licensing Deal for Radioligand Cancer Therapy

Sanofi has entered into an exclusive licensing agreement with RadioMedix, Inc., a U.S.-based biotechnology company developing radiopharmaceuticals for PET imaging and targeted alpha therapy (TAT), and Orano Med, a French subsidiary of the Orano Group focused on lead-212 (212Pb) radioligand…

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Allergan Aesthetics Launches BOTOX Cosmetic for Masseter Muscle Prominence in Adults in China

Allergan Aesthetics, a subsidiary of AbbVie (NYSE: ABBV), has announced that BOTOX® Cosmetic (onabotulinumtoxinA) is now available in China for the treatment of masseter muscle prominence (MMP). The masseter muscle, located in the lower face, is involved in chewing, and…

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Ncardia Introduces Ready-to-Use Assay Panel for Efficient Therapeutic Candidate Screening and Selection

Ncardia, a leading human iPSC company, has announced the launch of a new panel of ready-to-use assays aimed at streamlining the screening and selection of therapeutic candidates, with a particular focus on neurodegenerative diseases. This innovative panel offers standardized, robust,…

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Neurocrine Biosciences Announces Positive Phase 2 Results for NBI-1117568 in Adults with Schizophrenia

The NBI-‘568-SCZ2028 dose-finding study successfully met its primary endpoint with the once-daily 20 mg dose. This dose showed a significant and clinically meaningful reduction in the Positive and Negative Syndrome Scale (PANSS) total score at Week 6, achieving a placebo-adjusted…

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