已收盘 05-22 16:00:00 美东时间
-0.210
-5.30%
今日重点评级关注:HC Wainwright & Co.:维持Autolus Therapeutics"买入"评级,目标价从9美元升至10美元;Maxim Group:维持Rezolute"买入"评级,目标价从4美元升至10美元
05-15 10:49
Maxim Group analyst Anthony Vendetti maintains SeaStar Medical Holding (NASDAQ:ICU) with a Buy and raises the price target from $6 to $8.
05-15 04:45
On Wednesday, SeaStar Medical Holding (NASDAQ:ICU) discussed first-quarter fina...
05-14 05:20
SeaStar Medical Holding (NASDAQ:ICU) reported quarterly losses of $(0.90) per share which missed the analyst consensus estimate of $(0.82) by 9.76 percent. This is a 79.45 percent increase over losses of $(4.38) per
05-14 04:09
Companies Reporting Before The Bell • Similarweb (NYSE:SMWB) is estimated to re...
05-13 19:11
SeaStar Medical announced new data from the SAVE Registry, showing no device-related adverse events and strong survival rates in pediatric patients with AKI and sepsis treated with its SCD therapy. In vitro research highlights the device's immunomodulatory effects, shifting monocytes to an anti-inflammatory state. The company also hosted a symposium on pediatric AKI innovation, underscoring its leadership in this field.
03-30 12:20
SeaStar Medical Holding (NASDAQ:ICU) reported quarterly losses of $(0.80) per share which beat the analyst consensus estimate of $(1.01) by 21.18 percent. This is a 91.11 percent increase over losses of $(9.00) per share
03-26 04:07
Companies Reporting Before The Bell • Chewy (NYSE:CHWY) is expected to report q...
03-25 19:11
SeaStar Medical Holding Corporation will report its Q4 and year-end 2025 financial results on March 25, 2026, and host a webcast and conference call at 4:30 p.m. ET to discuss its financial performance and business progress. The webcast and call registration details are available online. The company, focused on treating critically ill patients with organ failure, markets QUELIMMUNE (SCD-PED) for life-threatening AKI in pediatric patients and is c...
03-18 20:05
SeaStar Medical announced the completion of patient enrollment in the FDA-required SAVE Registry, a post-approval study to confirm the safety of QUELIMMUNE therapy for children with AKI due to sepsis. With 50 patients enrolled, the company will report 28-day safety data to the FDA later this year. QUELIMMUNE, approved in 2024, has shown promising results in clinical trials, including a 77% survival rate in treated patients, and is being used in l...
03-05 13:20