CytoSite Bio, a developer of novel radiopharmaceuticals to help quantify and modulate immune activation to improve cancer immunotherapy, announced on Wednesday that has entered into a collaboration agreement with Lantheus Holdings Inc, the parent company of Lantheus Medical Imaging Inc.
The collaboration covers the clinical development and potential commercialisation of CytoSite's investigational Phase 1 ready granzyme B-targeted Positron Emission Tomography (PET) imaging tracer.
Additionally, Lantheus is granted an exclusive option to license global rights to CytoSite's novel imaging technology.
The two companies are collaborating on clinical development, with Lantheus having the option to acquire exclusive global rights for further development and commercialisation of the product. Under the agreement, CytoSite is eligible to receive payments for development, regulatory and commercial milestones, and royalties on future product sales.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA