Cellectar Biosciences Reports Second Quarter 2025 Financial Results and Provides a Corporate Update
Intend to Pursue an NDA Submission to the U.S. FDA under Accelerated Approval Pathway for Iopofosine I 131 for the Treatment of Waldenstrom Macroglobulinemia (WM) Subject to Sufficient Funding and ...
What are the key risks (clinical, regulatory, financial) that could affect the success of the Iopofosine program?
What is the likely impact on analyst consensus estimates and target price after this corporate update?
How might the outcome of the confirmatory trial affect the company’s long‑term strategic positioning and partnership opportunities?
13 days ago