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Vyvgart Hytrulo gains first APAC approval in China, redefining CIDP care: GlobalData

Express Pharma

Additionally, it is approved in the EU for gMG and in Japan for gMG and primary immune thrombocytopenia (ITP) under brand names Vyvgart and Vyvdura. per cent from 56,009 in 2023 to 56,163 in 2027.

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Astellas licenses companion drug for Pompe gene therapy

pharmaphorum

Other IgG proteases are being developed to tackle the issue of pre-existing immunity against AAV, but according to Selecta chief executive Carsten Brun these tend to be derived from common human pathogens – which means they themselves can be the target of existing antibodies.

Immunity 119
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Treatment options for Crohn’s disease expand after Rinvoq approval

Pharmaceutical Technology

The US Food and Drug Administration (FDA) has approved AbbVie’s Rinvoq (upadacitinib) for patients with Crohn’s disease who do not respond to TNF blockers, a common immune suppressant treatment for the condition.

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Transforming oncology with antibody therapeutics

European Pharmaceutical Review

According to Research and Markets 8 , the market for bispecific antibodies for cancer is forecasted to grow by $400 million during 2022-2027, due to the increasing prevalence of cancer worldwide. Overall, the mechanisms of action for amivantamab include ligand blocking, receptor degradation, and immune cell-mediated activity.

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Cambridge Cognition buys vocal biomarker firm Winterlight

pharmaphorum

Its vocal biomarkers are already being used to gauge the effect of drug treatments for dementia, including in the phase 2 TAURIEL trial of Roche/AC Immune’s’s tau protein-targeted antibody semorinemab. million) to its top-line in 2023 with “considerable growth” next year.

Immunity 105
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HepaStem seems most promising pipeline agent for decompensated cirrhosis due to NASH: GlobalData

Express Pharma

tumor formation, immune reactions, and therapy failure). HepaStem is projected to hit the US market in Q1 2027, while BioVie’s BIV201 is anticipated to be marketed in Q4 2028. Albutein appears to be on track to be the first therapeutic approved for DC, with a projected US launch date in Q1 2026.

Diabetes 111
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Moving towards oral delivery of biologics

European Pharmaceutical Review

1 Used to treat a range of chronic diseases (eg, diabetes, rheumatoid arthritis, psoriasis, Crohn’s disease, haemophilia, etc), it is projected that the sales of biologics will rise from $380 billion in 2022 to $416 billion in 2023, and to almost $600 billion in 2027.