Actinium Pharmaceuticals, Inc.

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CUSIP

00507W206
SEDOL

N/A
CIK

0001388320

www.actiniumpharma.com
LEI:
FIGI: BBG000RQZ245
ATNM

Actinium Pharmaceuticals, Inc.
GICS: - · Sector: Healthcare · Sub-Sector: Biotechnology
NAME
Actinium Pharmaceuticals, Inc.
ISIN
US00507W2061
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ATNM
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BLOOMBERG
ATNM US
EN 728x90
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The X-News Explorer is the ultimate source of information for investors with an affinity for the stock market who want to get a quick and convenient overview of the current news situation of a listed company. Various newswire services are available here. If a news alert is displayed, you will find company news that may be of interest to you. This service is provided by PR-Newswire.

Mon, 04.11.2024       Actinium Pharmaceuticals
US00507W2061

-       Dr. Almenoff brings more than 25 years of drug development and leadership experience to the Actinium Board of Directors  

-       Dr. Almenoff to join Actinium's Nominating and Corporate Governance Committee

NEW YORK, Nov. 4, 2024 /PRNewswire/ -- Actinium Pharmaceuticals, Inc. (NYSE AMERICAN: ATNM) (Actinium or the Company), a leader in the development of Antibody Radiation Conjugates (ARCs) and other targeted radiotherapies, today announced the appointment of June Almenoff, M.D., Ph.D. to its Board of Directors. Dr. Almenoff is an accomplished biopharma executive with over 25 years of senior leadership and drug development experience. She currently serves as a Board Director and advisor to numerous biopharma companies. 

Actinium Pharmaceuticals
Wed, 25.09.2024       Actinium Pharmaceuticals
US00507W2061

NEW YORK, Sept. 25, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Actinium Pharmaceuticals, Inc. ("Actinium" or the "Company") (NYSE: ATNM). Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.

The investigation concerns whether Actinium and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. 

Actinium Pharmaceuticals
Fri, 20.09.2024       Actinium Pharmaceuticals
US00507W2061

Iomab-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 approachesSIERRA achieved durable Complete Remission primary endpoint and Event-Free Survival secondary endpoint with high statistical significanceIomab-B was well tolerated in the older, heavily pretreated relapsed/refractory AML patients with active disease enrolled in the SIERRA trialActinium to seek strategic partner for Iomab-B for further development in the U.S. following completion of interactions with FDA for additional head-to-head clinical trial to demonstrate overall survival benefit
Actinium Pharmaceuticals
Wed, 18.09.2024       Actinium Pharmaceuticals
US00507W2061

NEW YORK, Sept. 17, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Actinium Pharmaceuticals, Inc. ("Actinium" or the "Company") (NYSE: ATNM). Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.

The investigation concerns whether Actinium and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. 

Actinium Pharmaceuticals
Tue, 10.09.2024       Actinium Pharmaceuticals
US00507W2061

NEW YORK, Sept. 9, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Actinium Pharmaceuticals, Inc. ("Actinium" or the "Company") (NYSE: ATNM). Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.

The investigation concerns whether Actinium and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. 

Actinium Pharmaceuticals
Wed, 04.09.2024       Actinium Pharmaceuticals
US00507W2061

NEW YORK, Sept. 3, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Actinium Pharmaceuticals, Inc. ("Actinium" or the "Company") (NYSE: ATNM).  Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.

The investigation concerns whether Actinium and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. 

Actinium Pharmaceuticals
Tue, 27.08.2024       Actinium Pharmaceuticals
US00507W2061

NEW YORK, Aug. 26, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Actinium Pharmaceuticals, Inc. ("Actinium" or the "Company") (NYSE: ATNM). Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.

The investigation concerns whether Actinium and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. 

Actinium Pharmaceuticals
Sun, 18.08.2024       Actinium Pharmaceuticals
US00507W2061

NEW YORK, Aug. 17, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Actinium Pharmaceuticals, Inc. ("Actinium" or the "Company") (NYSE: ATNM). Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.

The investigation concerns whether Actinium and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. 

Actinium Pharmaceuticals
Fri, 09.08.2024       Actinium Pharmaceuticals
US00507W2061

NEW YORK, Aug. 9, 2024 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Actinium Pharmaceuticals, Inc. ("Actinium" or the "Company") (NYSE: ATNM). Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.

The investigation concerns whether Actinium and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. 

Actinium Pharmaceuticals
Mon, 05.08.2024       Actinium Pharmaceuticals
US00507W2061

FDA determined that the Phase 3 SIERRA trial is not adequate to support a BLA filing for Iomab-B despite its statistically significant primary endpointAdditional head-to-head randomized clinical trial demonstrating overall survival benefit with Iomab-B is required by FDA to support a BLA filingActinium to request a meeting with the FDA to further discuss specifics of additional trialActinium will seek strategic partner for Iomab-B in the U.S. following completion of FDA interactions and focus development efforts on Actimab-A, Iomab-ACT and preclinical programs
Actinium Pharmaceuticals
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