XBiotech's Vilamakitug Enters Phase II Trial for Axial SpA
The IND application completed its 30-day FDA review without a clinical hold, opening U.S. patient enrollment for the an…
The IND application completed its 30-day FDA review without a clinical hold, opening U.S. patient enrollment for the an…
The 30-day FDA review with no clinical hold signals a clear regulatory path forward for the IL-1α–targeting monoclonal …
The findings reinforce cortisol modulation as a credible clinical target — and raise formulation questions for the adap…
The characterization study aims to quantify how long the biopolymer barrier persists in the nasal cavity — a critical c…
The dual-targeting CD19/CD20 mechanism marks a potential first-in-class approach, though the asset sits outside convent…
Gut-inflammation targeting moves further into clinical validation — with implications for next-gen functional ingredien…
The appearance marks a cross-sector moment as biotech pipelines intersect with functional and nutraceutical research in…
The open-label study design and 6-month topline readout signal an accelerated path toward regulatory submission for the…
Interim RECIST v1.1 data from Context Therapeutics positions CTIM-76 as a clinical-stage candidate in a heavily pre-tre…
The allowances cover both composition-of-matter and method-of-use claims, strengthening IP position in the emerging inn…
The Saudi hospital's presentation signals growing crossover between precision diagnostics and functional health monitor…
The MHRA approval expands emergency allergy management options for a pediatric population where needle-based delivery h…