Bluebird Bio Inc ( BLUE )
Seite 2 von 19 Neuester Beitrag: 13.12.24 23:38 | ||||
Eröffnet am: | 09.12.14 01:51 | von: NikGol | Anzahl Beiträge: | 463 |
Neuester Beitrag: | 13.12.24 23:38 | von: RichyBerlin | Leser gesamt: | 171.345 |
Forum: | Hot-Stocks | Leser heute: | 29 | |
Bewertet mit: | ||||
Seite: < 1 | | 3 | 4 | 5 | 6 | 7 | 8 | 9 | ... 19 > |
Das ist keine Empfehlung meinerseits, sondern soll lediglich ein freundschaftlicher Rat sein.
https://apnews.com/0ca64ab1a5f84af985934618cbe342d5
Ist in den USA nicht unüblich nach starken Kursrückgängen
Meine Meinung
Bluebird Bio meldet Zahlen für 2018
- Umsätze 54 Mio. $
- Verlust 556 Mio. $
- Cash 1,89 Mrd. $
http://investor.bluebirdbio.com/news-releases/...-year-2018-financial
Zynteglo bekommt Zulassung in Europa
https://www.fiercepharma.com/pharma/...humbs-up-thalassemia-treatment
"In Rekordzeit hat die Europäische Arzneimittelagentur EMA die Gentherapie Zynteglo der US-Biotech-Firma Bluebird Bio zugelassen. Hergestellt wird das Zelltherapeutikum in München – von der Apceth Biopharma GmbH."
...
https://transkript.de/news/...glo-im-schnellverfahren-zugelassen.html
Zynteglo Preis für Europa festgelegt
https://www.fiercepharma.com/pharma/...europe-to-be-paid-over-5-years
positive Gentherapie-Daten
http://www.pharmatimes.com/news/...positive_gene_therapy_data_1302258
Chief strategy Officer geht
http://investor.bluebirdbio.com/news-releases/...tegy-officer-jeffrey
February 22, 2020
ORLANDO — LentiGlobin gene therapy led to substantial reductions of sickle hemoglobin and considerable improvement in key markers of hemolysis, according to updated results from the phase 1/phase 2 HGB-206 study presented at TCT | Transplantation & Cellular Therapy Meetings.
https://www.healio.com/hematology-oncology/...ere-sickle-cell-disease
https://www.fool.com/investing/2020/03/04/...aire-making-biotech.aspx
"..bluebird: The company’s EU-approved beta-thalassemia gene-therapy Zynteglo is set to suffer another delay in the United States. Last month, Cambridge, Massachusetts-based bluebird said it expected to complete its US application to market the beta-thalassemia treatment in the United States only by the second half of this year, versus its previous estimate of the first half of 2020, due to the FDA asking for additional “information regarding various release assays.”
Now, in the context of the ongoing pandemic, the company on Thursday said it “does not anticipate completing the rolling BLA submission for LentiGlobin for β-thalassemia until mid-2021..”
https://endpts.com/...pandemic-regeneron-relaxes-eylea-payment-terms/
-
Chart;
Zahlen für Q1/20
- Revised Operating Plan achieves cash savings of over $500 million through 2022
- Company extends cash runway into 2022
http://investor.bluebirdbio.com/news-releases/...-business-update-and
BMS und bluebird erhalten ein Ablehnungsschreiben von der FDA
https://www.fool.com/investing/2020/05/13/...-refuse-to-file-let.aspx
5 Nutzer wurden vom Verfasser von der Diskussion ausgeschlossen: nahkauf, w.k.walter, Bishop of Diebach, Robin, Tommy2015