等待开盘 04-01 09:30:00 美东时间
+0.500
+4.60%
Tilray (TLRY) is expected to report an 8% jump in its revenue during its third-quarter results on March 31, before the market opens. The consensus EPS Estimate is $0.07, while revenue is expected to c...
03-31 22:34
T1 Energy press release (TE): Q4 GAAP EPS of -$0.70 misses by $0.69. Revenue of $358.55M (vs. $2.94M Y/Y) misses by $9.65M. As of December 31, 2025, T1 had cash, cash equivalents, and restricted cash ...
03-31 18:06
Seeking Alpha More on Virgin Galactic Virgin Galactic: Cash Runway Falls Short Of Its Commercialization Timeline Virgin Galactic GAAP EPS of -$0.98 beats by $0.07, revenue of $0.31M misses by $0.1...
03-31 04:19
Terrestrial Energy Inc. press release (IMSR): FY GAAP EPS of -$0.39. As of December 31, 2025, the company held approximately $298 million in cash and short-term investments. 2026 Outlook: The Company ...
03-30 19:08
Nike is due to report fiscal third-quarter results after the close on March 31, with Wall Street analysts expecting revenue of $11.2B and EPS of $0.28, down from last year's mark of $0.54. Key themes ...
03-30 18:30
Growing Clinical Evidence and Physician Adoption Broaden NanoKnife IRE Technology as Treatment Option for Major Solid Tumor TypesAngioDynamics, Inc. (NASDAQ:ANGO), a leading and transformative medical technology company
02-19 21:43
AngioDynamics expands NanoKnife indications in Europe for liver, pancreas, kidney and prostate tumors AngioDynamics Inc. announced expanded European indications for its NanoKnife System to include soft tissue ablation for tumors of the liver, pancreas, kidney, and prostate, including in patients wit
02-19 21:31
EU expands AngioDynamics NanoKnife indications for multi-organ tumor ablation AngioDynamics Inc. said European indications for its NanoKnife System have been expanded to include soft tissue ablation for tumors of the liver, pancreas, kidney and prostate, including use in patients with intermediate-r
02-19 21:31
AngioDynamics Secures FDA IDE Approval and Expanded 510(k) Clearance for AlphaVac System AngioDynamics Inc. announced that it received FDA approval in November 2025 for its Investigational Device Exemption (IDE) application for the APEX-Return pivotal study. This study will evaluate the safety and e
02-03 21:02
FDA genehmigt IDE-Antrag von AngioDynamics für APEX-Return-Studie AngioDynamics Inc. hat im November 2025 die Genehmigung der US-amerikanischen Food and Drug Administration (FDA) für den IDE-Antrag zur APEX-Return-Studie erhalten. In der Studie wird die Sicherheit und Wirksamkeit des AlphaReturn Blo
02-03 21:02