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Cellectar BioSciences Presents Phase 3 Confirmatory Trial Plans for Iopofosine in Waldenström's Macroglobulinemia

PUBT·10/20/2026 22:24:01
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Cellectar BioSciences Presents Phase 3 Confirmatory Trial Plans for Iopofosine in Waldenström's Macroglobulinemia
  • Cellectar BioSciences plans to submit a US accelerated approval application for iopofosine I 131 in Waldenström macroglobulinemia in the first half of 2027.
  • Potential US accelerated approval is targeted for the second half of 2027.
  • The 200-patient Phase 3 confirmatory trial projects first enrollment in the first quarter of 2027, with an estimated total cost of $42 million.
  • Phase 2b data showed an 83.6% overall response rate and a 61.8% major response rate in 55 evaluable patients.
  • Median response duration reached 17.8 months; median progression-free survival was 13.5 months.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Cellectar BioSciences Inc. published the original content used to generate this news brief on October 20, 2026, and is solely responsible for the information contained therein.