等待開盤 04-02 09:30:00 美东时间
+0.120
+2.20%
Savara Inc. (Nasdaq: SVRA) (the Company), a clinical stage biopharmaceutical company focused on rare respiratory diseases, today announced that the EMA has validated the submission of the MOLBREEVI MAA in autoimmune PAP;
03-30 20:16
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03-24 10:29
Savara press release (SVRA): Q4 GAAP EPS of -$0.13. Research and development expenses for the fourth quarter of 2025 and 2024 were $20.9 million and $23.3 million, respectively. General and administra...
03-14 03:28
Savara Inc. to Relocate Headquarters to Yardley, Pa Savara Inc. said it plans to relocate its headquarters to a new leased office at 19 W. College Avenue, Suite 200, Yardley, Pennsylvania. The company entered into the lease on March 10, 2026, for about 10,795 square feet, with the term set to run fr
03-13 20:33
Savara (NASDAQ:SVRA) reported quarterly losses of $(0.13) per share which met the analyst consensus estimate. This is unchanged from the same period last year.
03-13 20:20
Savara Q4 net loss widens as expenses rise Overview US rare disease drug developer's Q4 net loss widened yr/yr as expenses rose General and administrative expenses increased due to workforce expansion and commercial planning Company achieved key regulatory milestones for MOLBREEVI in US and Europe O
03-13 20:15
BRIEF-Savara Q4 Net Income USD -32.236 Million Mar 13 (Reuters) - Savara Q4 operating expenses USD 33.419 million. Q4 income from operations USD -33.419 million Q4 EPS USD -0.13
03-13 20:05
-- Day 74 Letter Received from the U.S. Food and Drug Administration (FDA) Indicated the Agency Has No Plans to Convene an Advisory Committee ---- Company has Submitted the Marketing Authorization Application (MAA) to
03-07 05:08
The U.S. FDA will review Savara's (SVRA) resubmitted BLA for Molbreevi (molgramostim inhalation solution) to treat the rare lung disease autoimmune pulmonary alveolar proteinosis. The agency granted p...
02-21 05:42
Savara Inc. (Nasdaq: SVRA) (the Company), a clinical-stage biopharmaceutical company focused on rare respiratory diseases, announced the FDA has filed for review the BLA for MOLBREEVI as a therapy to treat patients with
02-21 05:17