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BioNxt Solutions advances its sublingual cladribine program for MS, targeting a 2026 human trial after key manufacturing steps and a 2025 pig study.
BioNxt Solutions Inc. has advanced its sublingual cladribine program (BNT23001) for multiple sclerosis, completing key manufacturing and analytical method transfers to its European CDMO.
The active pharmaceutical ingredient has been ordered and is en route for pilot batch production of clinical-grade thin-film products.
The company is optimizing processes ahead of a pig bioavailability study beginning in October 2025, a critical preclinical step to validate absorption and dosing.
A first-in-human pilot study is planned for early 2026, following successful completion of this study.
The reformulation aims to improve bioavailability and patient adherence over traditional oral forms.
The company continues to pursue accelerated U.S. patent review and global intellectual property protection.
BioNxt Solutions avanza en su programa de cladribina sublingual para la EM, dirigido a un ensayo en humanos en 2026 después de pasos clave de fabricación y un estudio en cerdos en 2025.