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Venus Medtech concludes patient enrolment for Venus-PowerX trial

The study aims to assess the safety, efficacy and device performance of the Venus-PowerX in severe aortic stenosis patients.

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Dosing commences in Bio-Thera’s Phase I solid tumour study of BAT8013

The Phase I trial aims to determine maximum tolerated dose, evaluate pharmacokinetics, and gather preliminary efficacy data.

FDA grants fast track designation for Lundbeck’s Lu AH69593

Lu AH69593 is currently being studied in a Phase Ib clinical trial focused on patients with narcolepsy.

Affinia Therapeutics receives FDA orphan drug designation for AFTX-201

AFTX-201 is an investigational gene therapy delivered through a single intravenous infusion.