Precision BioSciences Inc
WKN: A400AS / ISIN: US74019P2074Precision Bio aufwärts mit neuer WKN
| eröffnet am: | 14.02.24 20:50 von: | moneywork4me |
| neuester Beitrag: | 29.12.25 11:31 von: | Highländer49 |
| Anzahl Beiträge: | 28 | |
| Leser gesamt: | 11194 | |
| davon Heute: | 6 | |
bewertet mit 1 Stern |
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14.02.24 20:50
#1
moneywork4me
Precision Bio aufwärts mit neuer WKN
Selten genug dass eine Aktie nach Resplit aufwärts geht, hoffe das bleibt so
https://www.nasdaq.com/de/market-activity/stocks/dtil/real-time
https://www.finanznachrichten.de/...ien/precision-biosciences-inc.htm
https://precisionbiosciences.com/
https://www.nasdaq.com/de/market-activity/stocks/dtil/real-time
https://www.finanznachrichten.de/...ien/precision-biosciences-inc.htm
https://precisionbiosciences.com/
2 Postings ausgeblendet.
28.02.24 20:14
#8
Balu4u
Kennt aktuell nur eine Richtung
Die Kurzziele wurden auch umgestellt
https://www.nasdaq.com/market-activity/stocks/dtil/analyst-research
https://www.nasdaq.com/market-activity/stocks/dtil/analyst-research
04.04.24 19:07
#10
Balu4u
Hier mal die Kursziele
https://www.nasdaq.com/articles/...biosciences-dtil%3A-heres-what-you
16.12.24 21:51
#12
Balu4u
Gute Zusammenfassung
https://de.investing.com/news/company-news/...iences-bei-93CH-2762645
17.12.24 13:11
#15
mirko75
Bei
Den anderen bestimmt. Aber der Verfall hier ist schon enorm. Über 50% in 3 Monaten. Auf der anderen Seite, bei den wenigen Stücken am Markt, könnte es eine 300-400% Rakete werden bei positiven Nachrichten. ..aber so'n Boden, dürften wir trotzdem mal bald gerne sehen......
18.12.24 14:27
#18
mirko75
Neuigkeiten
Ob Kursrelevant ?? ..Mal schauen... Precision BioSciences Receives Approval in Hong Kong to Expand PBGENE-HBV Phase 1 ELIMINATE-B Trial for the Treatment of Chronic Hepatitis B
- Approval in Hong Kong marks the first clinical trial application clearance of an in vivo gene editing approach for chronic hepatitis B in Hong Kong and the second CTA approval for PBGENE-HBV in 2024
- ELIMINATE-B is a global, multi-site study now actively recruiting patients; expected to report clinical data as it matures throughout 2025
- U.S. investigational new drug (IND) anticipated in 2025
December 18, 2024 07:01 AM Eastern Standard Time
DURHAM, N.C.--(BUSINESS WIRE)--Precision BioSciences, Inc. (Nasdaq: DTIL), a clinical stage gene editing company utilizing its novel proprietary ARCUS® platform to develop in vivo gene editing therapies for sophisticated gene edits, today announced that it has received Clinical Trial Application (CTA) approval in Hong Kong to study PBGENE-HBV in the ongoing ELIMINATE-B Phase I trial. PBGENE-HBV is Precision’s lead wholly owned in vivo gene editing program designed to cure chronic hepatitis B by eliminating cccDNA, the key source of replicating hepatitis B virus (HBV), and inactivating integrated HBV DNA in hepatocytes. The company is actively recruiting patients for the ELIMINATE-B trial in Moldova and has begun activating a top infectious disease clinical site in Hong Kong as part of its global regulatory and clinical operations strategy.
“We are pleased to receive our second CTA approval for PBGENE-HBV, expanding our ELIMINATE-B trial into a world-class HBV clinical trial site in Hong Kong”
Post this
“We are pleased to receive our second CTA approval for PBGENE-HBV, expanding our ELIMINATE-B trial into a world-class HBV clinical trial site in Hong Kong,” said Dr. Murray Abramson, Senior Vice President, Head of Clinical Development of Precision BioSciences. “PBGENE-HBV has been designed to target a viral site that is prevalent across all HBV genotypes, including in Asia, and we believe that this will enable us to evaluate and provide access to as many patients as possible. In addition to Hong Kong, our clinical trial site in Moldova continues to execute as planned, and we look forward to sharing clinical data as it matures throughout 2025.”
- Approval in Hong Kong marks the first clinical trial application clearance of an in vivo gene editing approach for chronic hepatitis B in Hong Kong and the second CTA approval for PBGENE-HBV in 2024
- ELIMINATE-B is a global, multi-site study now actively recruiting patients; expected to report clinical data as it matures throughout 2025
- U.S. investigational new drug (IND) anticipated in 2025
December 18, 2024 07:01 AM Eastern Standard Time
DURHAM, N.C.--(BUSINESS WIRE)--Precision BioSciences, Inc. (Nasdaq: DTIL), a clinical stage gene editing company utilizing its novel proprietary ARCUS® platform to develop in vivo gene editing therapies for sophisticated gene edits, today announced that it has received Clinical Trial Application (CTA) approval in Hong Kong to study PBGENE-HBV in the ongoing ELIMINATE-B Phase I trial. PBGENE-HBV is Precision’s lead wholly owned in vivo gene editing program designed to cure chronic hepatitis B by eliminating cccDNA, the key source of replicating hepatitis B virus (HBV), and inactivating integrated HBV DNA in hepatocytes. The company is actively recruiting patients for the ELIMINATE-B trial in Moldova and has begun activating a top infectious disease clinical site in Hong Kong as part of its global regulatory and clinical operations strategy.
“We are pleased to receive our second CTA approval for PBGENE-HBV, expanding our ELIMINATE-B trial into a world-class HBV clinical trial site in Hong Kong”
Post this
“We are pleased to receive our second CTA approval for PBGENE-HBV, expanding our ELIMINATE-B trial into a world-class HBV clinical trial site in Hong Kong,” said Dr. Murray Abramson, Senior Vice President, Head of Clinical Development of Precision BioSciences. “PBGENE-HBV has been designed to target a viral site that is prevalent across all HBV genotypes, including in Asia, and we believe that this will enable us to evaluate and provide access to as many patients as possible. In addition to Hong Kong, our clinical trial site in Moldova continues to execute as planned, and we look forward to sharing clinical data as it matures throughout 2025.”
18.12.24 16:10
#19
Balu4u
Geht weiter runter
Bald unter 4 Dollar?
Überlege ein Limit bei 3,50 zu platzieren
https://www.nasdaq.com/market-activity/stocks/dtil
Überlege ein Limit bei 3,50 zu platzieren
https://www.nasdaq.com/market-activity/stocks/dtil
19.12.24 18:31
#21
Balu4u
Eine der wenigen Biotechs
die heute grün ist. Nach dem Absturz ist aber auch eine Erholung überfällig. Hoffe es ist mehr als ein Strohfeuer
https://www.nasdaq.com/market-activity/stocks/dtil
https://www.nasdaq.com/market-activity/stocks/dtil
23.12.24 00:09
#22
moneywork4me
Könnte jetzt endlich wieder hoch gehen
https://de.investing.com/news/company-news/...n-hongkong-93CH-281745232874112
09.01.25 16:03
#23
mirko75
news
..iECURE Reports Complete Clinical Response in First Infant Dosed with its In Vivo Gene Editing Candidate ECUR-506 in an Ongoing Phase 1/2 Clinical Trial in Ornithine Transcarbamylase (OTC) Deficiency
First in vivo gene insertion clinical trial dosing infants reports complete clinical response in the first participant at the lowest dose level (1.3 x 1013 GC/kg) of ECUR-506 from three months post exposure to the end of study (six months post exposure) as demonstrated by the removal of standard of care ammonia scavenging medicines, followed by absence of hyperammonemic crises and normalization of protein intake
The OTC-HOPE Phase 1/2 trial has regulatory authorization in four geographies (US, UK, Spain and Australia) and is currently enrolling with the complete data readout anticipated in 1H 2026
ECUR-506 for neonatal onset OTC deficiency represents a meaningful potential clinical and commercial opportunity, affecting over 1,000 births per year globally
First in vivo gene insertion clinical trial dosing infants reports complete clinical response in the first participant at the lowest dose level (1.3 x 1013 GC/kg) of ECUR-506 from three months post exposure to the end of study (six months post exposure) as demonstrated by the removal of standard of care ammonia scavenging medicines, followed by absence of hyperammonemic crises and normalization of protein intake
The OTC-HOPE Phase 1/2 trial has regulatory authorization in four geographies (US, UK, Spain and Australia) and is currently enrolling with the complete data readout anticipated in 1H 2026
ECUR-506 for neonatal onset OTC deficiency represents a meaningful potential clinical and commercial opportunity, affecting over 1,000 births per year globally
09.01.25 17:41
#25
Balu4u
Hier der Link dazu
https://investor.precisionbiosciences.com/...-clinical-response-first
27.10.25 17:18
#26
moneywork4me
Geht seit einiger Zeit wieder hoch .
https://www.nasdaq.com/market-activity/stocks/dtil32894361
29.12.25 11:31
#28
Highländer49
Precision BioSciences
Die Aktie von Precision BioSciences ist eines der wenigen Biotech-Papiere, die in diesem Jahr keinen Höhenflug erlebten. Im Gegenteil: Die Aktie hat ohne schlechte Unternehmensnews in den letzten Monaten deutlich verloren und notiert aktuell weit unter ihrem Cashwert. Lauert hier ein Super-Schnäppchen?
https://www.finanznachrichten.de/...-jetzt-super-schnaeppchen-486.htm
https://www.finanznachrichten.de/...-jetzt-super-schnaeppchen-486.htm
