und die ODD-Meldung kommt in Sicht...seeeeehr bald.  

 

http://www.pharmacychoice.com/news/article.cfm?Article_ID=1532012

...
Company on track to transform profile from focus on early-stage to later-stage clinical development during 2016.

Actinium's profile is expected to change significantly in 2016 as the Company transitions to a later stage clinical development enterprise upon the start of the pivotal Phase 3 Iomab-B trial and the Phase 2 Actimab-A trial. S everal milestones are anticipated for the Company in 2016 including:


?Orphan Drug Designation for Iomab-B
?Clinical trial site and IRB contracts executed with top BMT centers
?Initiation of pivotal Phase 3 Iomab-B clinical
?Filing of EU Orphan Medicine Designation applications for Actimab-A
?Progress on EU Orphan Medicine application process for Iomab-B
?Initiation of Phase 2 portion of Actimab-A Phase 1/2 clinical trial
?Interim data from Actimab-A Phase 2 clinical trial
?Enrollment updates from Iomab-B clinical trial via Data Safety Monitoring Board readouts
?KOL days focused on Iomab-B and Actimab-A, respectively
?Pipeline and strategic initiative updates Actinium entered 2016 with a strong balance sheet with approximately $25 million cash and has built a team comprised of highly motivated and experienced professionals led by proven pharmaceutical executives. These strengths along with a dedication to improving the lives of Acute Myeloid Leukemia patients and patients suffering from other difficult to treat cancers with targeted payload immunotherapeutics will drive the Company's efforts in 2016.  

http://www.bionapcfa.com/2016/03/...ors-success-in-aml-means-for.html

...

Beyond the patient subsets by age or disease progression, there is significant cytogenic variation between AML patients that make various subsets respond and not respond to standard induction. I think Actinium has the potential to be the next Celator, and I'm keeping a keen eye on the story in 2016.

 

nun muss nur noch der Kurs ausbrechen - ist überfällig als auch die News zum OD Status.  

im Moment juckt das den Kurs nicht so recht:
http://www.reuters.com/article/...edType=RSS&feedName=companyNews
 

aber wenn Börse immer logisch wäre, wären wir alle längst Millionäre :-)  

 

ODD is ja jetzt gegeben. Nächster Meilenstein die Phase 3 von Iomab-B... kommt vorher noch was großes?  

da stehen interessante Infos drin, hinsichtlich Laufzeit etc.
http://www.marketwired.com/press-release/...nyse-mkt-atnm-2112323.htm
 

abtaucht, muss der Inhalt des webinars zur Phase III nicht unbedingt berauschend gewesen sein. Weiß da jemand mehr?  

aber das Webinar ist unter einem Link auf der Website abrufbar...  

seit gestern Abend wo ich Stücke zu 1,77 Dollar bekam mit dabei ...

von Chart her ein guter Einstioegspunkt wie ich finde ....

 

Ist zwar erst eine Phase-Studie, aber es gibt positive News:
http://www.finanznachrichten.de/...om-phase-1-actimab-a-trial-020.htm
 

 

 

kann die Aktie ihre krasse Unterbewertung abbauen - ist wie eine Flasche Sekt die kräftig geschüttelt wurde - irgend wann knallt der Korken :-)  

Actinium jetzt auch schon eine Zeit!
Könnt ihr mir kurz schildern welche aussichtsreichen Produkte die Firma hat & welche Kursziele ihr bei positivem Ausgang habt :)  

http://ir.actiniumpharma.com/press-releases/...status-by-the-european

Aber leider verpufft jede Unternehmensmeldung . . .  

 

http://sleekmoney.com/...ating-from-analysts-at-roth-capital/1500367/

http://www.actiniumpharma.com/product-pipeline  

http://www.nasdaq.com/press-release/...-clinical-trial-20160921-00289  

...

http://www.newsmaker.com.au/news/115105/...ecast-to-2021#.V-U6GPDuKEc  

Actinium initiates mid-stage clinical trial of Actimab-A in patients with AML over age 60; shares rise 5% premarket


Sep 27 2016, 08:37 ET | About: Actinium Pharmaceuticals, ... (ATNM) | By: Mamta Mayani, SA News Editor    
 




Actinium Pharmaceuticals (ATNM) initiates a Phase 2 clinical trial of Actimab-A in patients newly diagnosed with Acute Myeloid Leukemia (AML) who are over the age of 60. Actimab-A, Actinium's most advanced alpha particle immunotherapy (APIT) program, consists of the CD33-targeting monoclonal antibody, HuM195, and the alpha-emitting radioisotope, Actinium-225.

Actinium-225 gives off high-energy alpha particles as it decays which kills cancer cells.

The open-label study will enroll 53 patients. The primary endpoint is the complete response rate defined as complete remission or complete remission with incomplete platelet recovery. The secondary endpoint is overall survival. Top-line data should be available in H2 2017.

Shares are up 5% premarket on modest volume.




http://seekingalpha.com/news/...ents-aml-age-60-shares-rise-5-percent