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WKN: A2QA48 | ISIN: US00507W2061 | Ticker-Symbol: 7AY1
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21.11.24
13:25 Uhr
1,304 Euro
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MoActinium Pharma Q3 Loss Narrows191WASHINGTON (dpa-AFX) - Actinium Pharmaceuticals Inc. (ATNM) Monday announced a narrower loss for the third quarter. The September quarter loss was $11.6 million, compared to $13.3 million a...
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MoActinium Pharmaceuticals reports Q3 results3
05.11.Actinium Pharmaceuticals, Inc. - 8-K, Current Report2
20.09.Actinium Pharmaceuticals, Inc.: Actinium Pharmaceuticals Announces Publication of Results from the Phase 3 SIERRA Trial of Iomab-B in the Journal of Clinical Oncology163Iomab-B is the first CD45 targeted radiotherapy for conditioning in development to enable potentially curative bone marrow transplant and represents an alternative to chemotherapy-based approaches SIERRA...
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06.08.Actinium's radioligand filing plans scuppered by FDA34
05.08.Actinium Pharmaceuticals, Inc. - 10-Q, Quarterly Report8
05.08.S&P 500 Down Over 100 Points; Actinium Pharmaceuticals Shares Plunge6
05.08.Actinium Pharmaceuticals Receives FDA Request For Additional Studies On Leukemia Treatment15
05.08.FDA sinks Actinium's radiotherapy blood cancer filing plans, prompting pivot to partnering19
05.08.Why Is Actinium Pharmaceuticals Stock Falling In Pre-market?373WASHINGTON (dpa-AFX) - Actinium Pharmaceuticals (ATNM) issued a regulatory update on the planned Biologics License Application filing for Iomab-B in patients with active relapsed or refractory...
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05.08.Actinium Pharmaceuticals, Inc. - 8-K, Current Report6
05.08.Actinium Pharmaceuticals, Inc.: Actinium Provides Regulatory Update on Planned BLA Filing and Future Plans for Iomab-B in the U.S.284FDA determined that the Phase 3 SIERRA trial is not adequate to support a BLA filing for Iomab-B despite its statistically significant primary endpoint Additional head-to-head randomized clinical...
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25.07.Actinium Pharmaceuticals, Inc.: Actinium Announces FDA Clearance of Iomab-ACT Targeted Conditioning IND Application for Sickle Cell Disease Patients Undergoing Bone Marrow Transplant in Collaboration with Columbia University133- Sickle cell disease affects approximately 100,000 patients in the U.S. annually and is a debilitating and life-threatening condition with high unmet need - Current conditioning with non-targeted...
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22.07.NorthStar, BWXT Sign Master Services Agreement Supporting Actinium-225 Production7
17.06.Actinium Pharma Reports Promising Initial Data Using Actimab-A With Menin Inhibitors357WASHINGTON (dpa-AFX) - Actinium Pharmaceuticals presented the first ever preclinical data from the combination of menin inhibitors with ARC Actimab-A in acute myeloid leukemia models. Menin...
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17.06.Actinium Pharmaceuticals, Inc.: Actinium Presents First Ever Data Demonstrating Actimab-A in Combination with Leading Menin Inhibitors Leads to Anti-Tumor Control and Potent Leukemic Cell Killing in Preclinical Acute Myeloid Leukemia Models at the 2024 EH129- Actimab-A enhances dose-dependent acute myeloid leukemia cell death in KMT2A sensitive acute myeloid leukemia blasts in combination with leading menin inhibitors- Combination with leading menin inhibitor...
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10.06.Actinium Pharmaceuticals, Inc.: Actinium Highlights Mutation Data from the Phase 3 SIERRA Trial of Iomab-B and Novel Linker Technology to Support Solid Tumor Antibody Radiation Conjugate Development at the 2024 Society of Nuclear Medicine & Molecular Imag159Iomab-B led bone marrow transplant improved survival in patients with high-risk relapsed or refractory acute myeloid leukemia including those with a TP53 mutation Iomab-B safely delivered radiation...
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07.05.Actinium Pharmaceuticals, Inc.: Actinium Announces KOL Webinar to Highlight Recently Announced Iomab-ACT Trial with Leading FDA Approved Commercial CAR T-Cell Therapy Being Led by the University of Texas Southwestern177Dr. Farrukh Awan, Professor of Medicine, Division of Hematology Oncology at University of Texas Southwestern and Principal Investigator for the trial to join Actinium management for webinar Expansion...
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01.04.Actinium Pharmaceuticals, Inc.: Actinium Announces Iomab-B Phase 3 SIERRA Trial Results Demonstrating Survival Benefit in High-Risk Relapsed or Refractory Acute Myeloid Leukemia Patients with TP53 Mutations Accepted for Oral Presentation at the 50th Europ228- The SIERRA results demonstrate Iomab-B's ability to overcome the negative impact of a TP53 mutation in patients who otherwise would have limited treatment options and dismal prognosis - Represents...
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26.03.Actinium Pharmaceuticals, Inc.: Actinium Announces Clinical Trial to Study Iomab-ACT Targeted Radiotherapy Conditioning with Leading FDA Approved Commercial CAR T-Cell Therapy140Potential blockbuster opportunity for next-generation targeted radiotherapy conditioning with CAR T-cell therapy a multi-billion market with six FDA approved therapies totaling sales over $3.5 billion...
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