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Actinium Reports Long-Term Safety Data for Actimab-A Plus CLAG-M in Relapsed or Refractory AML
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Actinium Reports Long-Term Safety Data for Actimab-A Plus CLAG-M in Relapsed or Refractory AML
  • Actinium Pharmaceuticals released a Phase 1 abstract evaluating long-term safety of Actimab-A with CLAG-M chemotherapy in relapsed or refractory acute myeloid leukemia.
  • Results will be presented at the American Society of Hematology annual meeting on December 13, 2026.
  • Safety findings support further evaluation of Actimab-A as a potential treatment backbone across mutations, with follow-up assessing blood-count recovery and delayed organ toxicity.
  • Efficacy results presented at ASH 2022 showed clinical activity in patients previously treated with venetoclax or whose leukemia carried TP53 mutations.


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. Actinium Pharmaceuticals Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: 202611040905PR_NEWS_USPR_____NY88514) on November 04, 2026, and is solely responsible for the information contained therein.

Disclaimer:This article represents the opinion of the author only. It does not represent the opinion of Webull, nor should it be viewed as an indication that Webull either agrees with or confirms the truthfulness or accuracy of the information. It should not be considered as investment advice from Webull or anyone else, nor should it be used as the basis of any investment decision.
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