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WKN: A3CPAK | ISIN: US04317A1079 | Ticker-Symbol:
NASDAQ
17.04.26 | 21:59
12,490 US-Dollar
+3,14 % +0,380
Branche
Biotechnologie
Aktienmarkt
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1-Jahres-Chart
ARTIVA BIOTHERAPEUTICS INC Chart 1 Jahr
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ARTIVA BIOTHERAPEUTICS INC 5-Tage-Chart

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11.03.Cantor Fitzgerald reiterates Artiva Biotherapeutics stock rating1
11.03.Artiva Biotherapeutics: Cantor Fitzgerald bekräftigt "Overweight"-Rating4
10.03.Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Reports Full Year 2025 Financial Results and Recent Business Highlights646Initial clinical response data for AlloNK in refractory rheumatoid arthritis (RA) expected in first half of 2026 U.S. Food and Drug Administration (FDA) interaction to discuss potential pivotal trial...
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10.03.Artiva Biotherapeutics, Inc. - 10-K, Annual Report1
10.03.Artiva Biotherapeutics, Inc. - 8-K, Current Report3
24.02.Artiva Biotherapeutics Names Thad Huston CFO3
24.02.Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Announces Appointment of Thad Huston as Chief Financial Officer and Award of Inducement Grant348SAN DIEGO, Feb. 24, 2026 (GLOBE NEWSWIRE) -- Artiva Biotherapeutics, Inc. (Nasdaq: ARTV) (Artiva), a clinical-stage biotechnology company whose mission is to develop effective, safe and accessible...
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ARTIVA BIOTHERAPEUTICS Aktie jetzt für 0€ handeln
19.02.Artiva Biotherapeutics, Inc. - 8-K, Current Report1
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 Disease28032 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 Highlights233Over 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-
16.10.25Artiva Biotherapeutics, Inc.: Artiva Biotherapeutics Announces Refractory Rheumatoid Arthritis as Lead Indication, Upcoming Data Releases, and Corporate Update455Prioritization 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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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 ...24164% (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 Highlights419IND 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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