Clarity Pharmaceuticals (ASX:CU6), an Australia-based clinical-stage radiopharmaceutical company, announced on Tuesday that it has entered into a commercial manufacturing agreement with SpectronRx for Clarity's lead diagnostic product, 64Cu-SAR-bisPSMA.
Under the agreement SpectronRx's facility in Indiana will provide on-demand commercial-scale manufacturing of both copper-64 and 64Cu-SAR-bisPSMA under one roof and enable distribution to all 50 US states. It can produce up to 400,000 patient-ready doses of 64Cu-SAR-bisPSMA annually from the one facility.
Clarity says that together with other supply and manufacturing deals, this agreement substantially bolsters reliable, universal access to 64Cu-SAR-bisPSMA in the United States for a commercial rollout upon successful completion of Phase III registrational trials and subsequent US Food and Drug Administration (FDA) New Drug Application (NDA) approval.
The commercial supply agreement is effective as of 17 June 2025, and is for an initial period of five years. Cancellation and extension provisions are aligned with industry standard rates.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval