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WKN: A0MKPR | ISIN: FR0010425595 | Ticker-Symbol: ZVA
Tradegate
20.09.24
18:05 Uhr
1,918 Euro
-0,107
-5,28 %
Branche
Biotechnologie
Aktienmarkt
Sonstige
1-Jahres-Chart
CELLECTIS SA Chart 1 Jahr
5-Tage-Chart
CELLECTIS SA 5-Tage-Chart
RealtimeGeldBriefZeit
1,9442,02022:59
1,9021,93822:00

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04.09.Cellectis Inc.: Monthly information on share capital and company voting rights2
03.09.Cellectis Presents Pre-Clinical Evidence of MUC1 CAR T-cells Reducing Triple-Negative Breast Cancer While Preserving Safety52 NEW YORK, Sept. 03, 2024 (GLOBE NEWSWIRE) -- Cellectis (the "Company") (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to...
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03.09.Cellectis S.A. - 6-K, Report of foreign issuer1
26.08.Cellectis Publishes a Molecular Therapy Article on a SMART DUAL CAR T-cell Approach for Treating Recalcitrant Solid Tumors3
26.08.Cellectis S.A. - 6-K, Report of foreign issuer1
09.08.Cellectis Non-GAAP EPS of -$0.22 beats by $0.09, revenue of $9.5M misses by $0.2M3
07.08.Cellectis names Adrian Kilcoyne as chief medical officer1
07.08.Cellectis Appoints Dr. Adrian Kilcoyne as Chief Medical Officer135NEW YORK, Aug. 07, 2024 (GLOBE NEWSWIRE) -- Cellectis (the "Company") (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to...
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06.08.Cellectis Provides Financial Results for the Second Quarter 2024170ODD and RPDD granted by the FDA and ODD granted by the European Commission to UCART22 for the treatment of ALLODD granted by the FDA to CLLS52 (alemtuzumab) for ALL treatmentCash position of $273...
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05.08.Cellectis Inc.: Monthly information on share capital and company voting rights1
02.08.Cellectis starts alemtuzumab revival with FDA orphan drug win in leukaemia3
01.08.Cellectis Inc.: FDA Grants Orphan Drug Designation to Cellectis' CLLS52 (alemtuzumab) For ALL Treatment110NEW YORK, Aug. 01, 2024 (GLOBE NEWSWIRE) -- Cellectis (the "Company") (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to...
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01.08.Cellectis S.A. - 6-K, Report of foreign issuer1
26.07.Cellectis' UCART22 Granted ODD and RPDD Status by FDA3
25.07.Cellectis Inc.: FDA Grants Orphan Drug and Rare Pediatric Disease Designation Status to Cellectis' UCART22 product candidate for Acute Lymphoblastic Leukemia (ALL) Treatment81ALL represents 10% of all leukemia cases in the United States, progresses rapidly, and is typically fatal within weeks or months if left untreated1There is an urgent need to develop new therapies...
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25.07.Cellectis S.A. - 6-K, Report of foreign issuer4
05.07.Cellectis Inc.: Monthly information on share capital and company voting rights2
28.06.Cellectis S.A. - 6-K, Report of foreign issuer3
20.06.Cellectis Publishes a Scientific Article Unveiling Three Key Factors for Efficient TALE Base Editing4
20.06.Cellectis S.A. - 6-K, Report of foreign issuer2
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