Clinical TrialsThe safety profile of iopofosine I-131 was positive and consistent with previous data, demonstrating high rates of response across challenging patient populations.
Financial PerformanceThe company has $34M in cash (above the market cap of ~$10M) and with reduced opex, should have runway into late 2025 and paths forward with earlier-stage assets on what is viewed as a de-risked PDC platform.
Regulatory ApprovalCellectar recently held a meeting with the FDA, which confirmed a clear path to accelerated approval for Iopofosine-131 in Waldenstrom’s macroglobulinemia.