Neupharma gains exclusive rights to develop and commercialize corticorelin for peritumoral brain edema
Phase I EPRAD study of DT-9081 demonstrated a favorable safety profile
The trial met its primary endpoint, demonstrating a statistically significant and clinically meaningful improvement in progression-free survival
Long-term OGSIVEO treatment for up to four years associated with further tumor reductions, increased objective response rate, sustained symptom improvement, and consistent safety profile
Takeda will make an upfront payment of $1.2 billion, which includes a $100 million equity investment in Innovent
Global Phase 3 MANEUVER study highlights ongoing benefits and consistent safety profile
The company will present new data from across over 20 cancer types and multiple treatment settings at European Society for Medical Oncology Congress 2025
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