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WKN: A3CPAK | ISIN: US04317A1079 | Ticker-Symbol:
NASDAQ
30.01.26 | 22:00
3,890 US-Dollar
-6,27 % -0,260
Branche
Biotechnologie
Aktienmarkt
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ARTIVA BIOTHERAPEUTICS INC Chart 1 Jahr
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ARTIVA BIOTHERAPEUTICS INC 5-Tage-Chart

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21.01.Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Announces Upcoming Presentations at the 2026 Transplantation & Cellular Therapy Meetings of ASTCT and CIBMTR (Tandem Meetings) Highlighting Cost-Effectiveness of AlloNK in a Community Rheumatology ...1
12.12.25Artiva Biotherapeutics, Inc. - 8-K, Current Report2
12.11.25Artiva BioTherapeutics GAAP EPS of -$0.883
12.11.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Announces Positive Initial Safety and Translational Data Supporting Deep B-Cell Depletion with AlloNK in Autoimmune Disease21432 patients with autoimmune disease treated with AlloNK plus anti-CD20 monoclonal antibody (mAb) as of October 1, 2025, data cutoff All patients received AlloNK as outpatients, and the majority were...
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12.11.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Reports Third Quarter 2025 Financial Results and Recent Business Highlights151Over 100 patients treated with AlloNK across autoimmune and oncology indications Refractory rheumatoid arthritis (RA) prioritized as lead indication following FDA Fast Track Designation for AlloNK®...
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12.11.25Artiva Biotherapeutics, Inc. - 10-Q, Quarterly Report-
12.11.25Artiva Biotherapeutics, Inc. - 8-K, Current Report-
17.10.25Cantor Fitzgerald reiterates Overweight rating on Artiva Biotherapeutics stock19
ARTIVA BIOTHERAPEUTICS Aktie jetzt für 0€ handeln
16.10.25Rheumatoide Arthritis: Artiva erhält FDA Fast-Track-Status für Zelltherapie AlloNK5
16.10.25Artiva Biotherapeutics stock soars after FDA Fast Track designation2
16.10.25Artiva's AlloNK receives FDA Fast Track status for rheumatoid arthritis3
16.10.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Announces Refractory Rheumatoid Arthritis as Lead Indication, Upcoming Data Releases, and Corporate Update370Prioritization of refractory rheumatoid arthritis (RA) as lead indication for AlloNK® development FDA Fast Track Designation received for AlloNK in refractory RA, representing the first drug candidate...
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07.08.25Artiva Biotherapeutics GAAP EPS of -$0.87 misses by $0.062
06.08.25Artiva Biotherapeutics, Inc. - S-8, Securities to be offered to employees in employee benefit plans1
06.08.25Artiva Biotherapeutics, Inc. - 10-Q, Quarterly Report1
06.08.25Artiva Biotherapeutics, Inc. - 8-K, Current Report1
13.05.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Announces Longer-term Phase 1/2 Data Demonstrating Prolonged Durability for AlloNK in Combination with Rituximab in Patients with B-cell-Non-Hodgkin Lymphoma at the ASGCT ...18964% (9/14) complete response rate with AlloNK + rituximab in heavily pretreated patients that were naïve to prior CAR-T cell therapy, in line with approved auto-CAR-T therapies in aggressive B-NHL...
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08.05.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Reports First Quarter 2025 Financial Results, Recent Business Highlights356IND clearance and initiation of global basket trial exploring AlloNK® + rituximab in refractory rheumatoid arthritis, Sjögren's disease, idiopathic inflammatory myopathies and systemic sclerosis ...
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08.04.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Appoints Subhashis Banerjee, M.D., as Chief Medical Officer841SAN DIEGO, April 08, 2025 (GLOBE NEWSWIRE) -- Artiva Biotherapeutics, Inc. (Nasdaq: ARTV), a clinical-stage biotechnology company whose mission is to develop effective, safe, and accessible cell therapies...
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24.03.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Reports Full Year 2024 Financial Results and Recent Business Highlights252Initial data for AlloNK® from autoimmune program expected H1 2025 Updated clinical data from Phase 1/2 trial exploring AlloNK + rituximab in NHL showing continued durability of response to be presented...
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