Stock Research for ATNM


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ATNM Stock Chart & Research Data

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ATNM Due diligence Resources & Stock Charts

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The Four Most Popular Resources

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Stock Analysis

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MarketWatch View the Analyst Estimates for ATNM - MarketWatch CNBC View the Earnings History for ATNM - CNBC
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Social Media Mentions

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Financial & Transaction Holdings

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Stock Charts

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Latest Financial News for ATNM

Actinium Forms Nuclear Medicine Focused Advisory Board to Facilitate Pipeline Clinical Development and Iomab-B Commercial Planning
Posted on Tuesday July 17, 2018

NEW YORK, July 17, 2018-- Actinium Pharmaceuticals, Inc., today announced that it has appointed the members of its Nuclear Medicine Clinical Advisory Board. The following nuclear medicine physicians and ...

Actinium to Host Webcast on July 10, 2018 to Discuss Actimab-A MRD clinical trial for Minimal Residual Disease in Postremission AML Patients
Posted on Monday July 09, 2018

Actinium Pharmaceuticals, Inc. (NYSE AMERICAN:ATNM) ("Actinium" or "the Company"), provided a reminder that it will host a webcast on July 10, 2018 at 8:00 AM ET. The webcast will discuss the Company’s previously announced Actimab-A MRD clinical trial for patients with AML who are in remission but have detectable minimal residual disease (MRD).

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Posted on Monday July 02, 2018

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Actinium Announces New Clinical Trial to Study Effect of Actimab-A on Minimal Residual Disease in Postremission AML Patients
Posted on Thursday June 28, 2018

Actinium Pharmaceuticals, Inc. (NYSE AMERICAN:ATNM) ("Actinium" or "the Company"), today announced that Dr. Joseph Jurcic, Director of the Hematologic Malignancies Section and Professor of Medicine at Columbia University Medical Center, has initiated Actimab-A MRD, a new clinical trial for patients with AML who are in remission but have detectable minimal residual disease (MRD).  The trial will study the safety/tolerability of Actimab-A in the postremission consolidation setting and include dose finding analyses.  The trial will also study the impact of Actimab-A on minimal residual disease (MRD) as well as progression-free (PFS) and overall survival (OS) rates. The investigational new drug (IND) application for this trial has been cleared by the FDA.

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