Laboratory services provider Labcorp (NYSE:LH) announced on Thursday a collaboration with the US Food and Drug Administration (FDA) and pharmaceutical research services provider Charles River Laboratories International Inc (NYSE:CRL) to advance the science used to evaluate a medicine's abuse potential, or the likelihood that it could be abused.
This research aims to support safer drug development and more informed regulatory decisions.
The collaboration brings together complementary expertise from industry and government. Labcorp will contribute its experience conducting regulatory abuse potential studies, while FDA scientists will conduct data analysis and contribute regulatory science expertise. Together, the organisations aim to advance the science used to evaluate the risk that a medicine could be abused using harmonised behavioural economics methodology to quantify and rank abuse potential.
Understanding how medicines and emerging substances may be used outside controlled settings is critical to protecting public health and informing regulatory decision-making, Labcorp said. The collaboration aims to advance the science used to assess abuse-related risks and generate evidence that may help improve the prediction of real-world use patterns.
Viatris' RYZUMVI receives US FDA Approval to treat presbyopia
Omeros receives negative EU opinion on narsoplimab after re-examination
Ionis' TRYNGOLZA recommended for EU approval in severe hypertriglyceridemia
FDA approves Genentech's Enspryng as first at-home subcutaneous treatment for thyroid eye disease
EMA issues positive CHMP opinion for Revolution Medicines' RASONQUE in metastatic pancreatic cancer
Edesa Biotech receives FDA clearance to expand EB06 vitiligo study into the US
LTR Pharma launches Roxus nasal spray for ED in the US
Genezen agrees manufacturing collaboration with Galibra Neuroscience
FDA grants Breakthrough Therapy Designation to Legacy Healthcare's CINAINU (LH-8)
FDA approves Vantis Vascular's 6F CrossFAST model
Blue Lake Biotechnology reports interim data from Phase 1/2a paediatric clinical trial of BLB201
ArkBio reports FDA clearance of IND application for AK0406
Agilent to acquire Proscia for up to USD270m to expand digital pathology capabilities