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Document And Entity Information - shares | 9 Months Ended | |
---|---|---|
Sep. 30, 2020 | Oct. 23, 2020 | |
Document Information Line Items | ||
Entity Registrant Name | Actinium Pharmaceuticals, Inc. | |
Document Type | 10-Q | |
Current Fiscal Year End Date | --12-31 | |
Entity Common Stock, Shares Outstanding | 13,586,525 | |
Amendment Flag | false | |
Entity Central Index Key | 0001388320 | |
Entity Current Reporting Status | Yes | |
Entity Filer Category | Non-accelerated Filer | |
Document Period End Date | Sep. 30, 2020 | |
Document Fiscal Year Focus | 2020 | |
Document Fiscal Period Focus | Q3 | |
Entity Small Business | true | |
Entity Emerging Growth Company | false | |
Entity Shell Company | false | |
Entity File Number | 001-36374 | |
Entity Incorporation, State or Country Code | DE | |
Entity Interactive Data Current | Yes |
Please wait while we load the requested 10-Q report or click the link below:
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Compare this 10-Q Quarterly Report to its predecessor by reading our highlights to see what text and tables were removed , added and changed by Actinium Pharmaceuticals, Inc..
Actinium Pharmaceuticals, Inc.'s Definitive Proxy Statement (Form DEF 14A) filed after their 2020 10-K Annual Report includes:
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A continuation or worsening of the levels of market disruption and volatility seen in the recent past could have an adverse effect on our ability to access capital, which could in the future negatively affect our liquidity.
Specifically, the ASU eliminates the need for us to assess whether a contract on the entity's own equity (1) permits settlement in unregistered shares, (2) whether counterparty rights rank higher shareholder's rights, and (3) whether collateral is required.
We believe our ARC approach is the most effective method to target CD45 positive cells, as the radioisotope payload linear energy transfer can readily ablate a targeted cell without requiring payload internalization like an antibody drug conjugate or without relying on biological effector function processes like a naked antibody.
We exercised a single ad hoc interim analysis in the second quarter of 2020 based on the data reported from SIERRA thus far that is consistent with prior findings with Iomab-B and have updated and shared the updated SIERRA trial protocol and statistical analysis plan with the FDA to reflect the single ad hoc interim analysis.
The decrease in expenses was primarily due to manufacturing related to the antibody component of Iomab-B, as in prior periods we have manufactured sufficient antibody supply for the SIERRA trial and other planned trials.
The decrease in expenses was...Read more
In the European Union ("EU"),...Read more
These factors include but are...Read more
General and administrative expenses of...Read more
Net loss of $5.5 million...Read more
Results with MSKCC's 19-28z CD-19...Read more
Research and development expenses decreased...Read more
Research and development expenses decreased...Read more
Currently, the Phase 3 SIERRA...Read more
Radiation is an effective therapeutic...Read more
These non-targeted conditioning regimens are...Read more
These items are monitored and...Read more
Early adoption of the ASU...Read more
The effective life of the...Read more
Such events may result in...Read more
Overall, transplant procedures in the...Read more
The amendments in this ASU...Read more
This ASU is effective January...Read more
Early adoption is permitted upon...Read more
I-131-Apamistamab has clinical proof of...Read more
Furthermore, in vivo studies in...Read more
The updated guidance improves the...Read more
Gross proceeds from this offering...Read more
Gross proceeds from this offering...Read more
The universal engraftment rate and...Read more
We believe our Iomab-ACT program...Read more
Unlike chemotherapy, Iomab-ACT is targeted...Read more
Such government-imposed precautionary measures may...Read more
Further, the continuation and/or resurgence...Read more
The interim analysis is expected...Read more
Financial Statements, Disclosures and Schedules
Inside this 10-Q Quarterly Report
Material Contracts, Statements, Certifications & more
Actinium Pharmaceuticals, Inc. provided additional information to their SEC Filing as exhibits
Ticker: ATNM
CIK: 1388320
Form Type: 10-Q Quarterly Report
Accession Number: 0001213900-20-033053
Submitted to the SEC: Fri Oct 23 2020 5:01:56 PM EST
Accepted by the SEC: Fri Oct 23 2020
Period: Wednesday, September 30, 2020
Industry: Pharmaceutical Preparations