iopofosine i 131

·Code: CLR 131

iopofosine i 131: developed by 1 company · 1 FDA decision. Updated within the last hour.

Development Pipeline (1)

FDA Decisions

FDA_MeetingEMA SAWP advised that filing for a Conditional Marketing Authorization for iopofosine I 131 in post-BTKi refractory Waldenstrom macroglobulinemia could be acceptable and met eligibility requirements.(CLRB)

Frequently asked questions

Who is developing iopofosine i 131?

iopofosine i 131 is being developed by Cellectar Biosciences, Inc..

What is iopofosine i 131's latest FDA decision?

The most recent tracked FDA decision for iopofosine i 131 is FDA_Meeting for EMA SAWP advised that filing for a Conditional Marketing Authorization for iopofosine I 131 in post-BTKi refractory Waldenstrom macroglobulinemia could be acceptable and met eligibility requirements..

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    iopofosine i 131 — Drug Pipeline, Trials & FDA Status | BioSniper