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Savara Inc

5.59
+0.10001.82%
Pre-market: 5.600.0100+0.18%05:37 EDT
Volume:3.04M
Turnover:16.95M
Market Cap:1.14B
PE:-9.67
High:5.64
Open:5.54
Low:5.50
Close:5.49
52wk High:7.01
52wk Low:3.08
Shares:204.66M
Float Shares:198.20M
Volume Ratio:1.85
T/O Rate:1.53%
Dividend:- -
Dividend Rate:- -
EPS(TTM):-0.5782
EPS(LYR):-0.5344
ROE:-105.48%
ROA:-50.15%
PB:7.96
PE(LYR):-10.46

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Savara Inc. to Relocate Headquarters to Yardley, Pa

Reuters
·
Mar 13

Savara Inc. publishes corporate presentation on autoimmune pulmonary alveolar proteinosis and MOLBREEVI Phase 3 data

Reuters
·
Mar 13

Savara Q4 EPS $(0.13), Inline

Benzinga Earnings
·
Mar 13

Earnings Flash (SVRA) Savara Posts Q4 Loss $0.13 a Share, vs. FactSet Est of $0.12 Loss

MT Newswires Live
·
Mar 13

CORRECTED-Savara Q4 net loss widens as expenses rise

Reuters
·
Mar 13

Savara FY 2025 net loss widens 24% to USD 118.84 million as G&A expenses jump 68% to USD 42.06 million

Reuters
·
Mar 13

BRIEF-Savara Q4 Net Income USD -32.236 Million

Reuters
·
Mar 13

Savara Reports Fourth Quarter and Year End 2025 Financial Results and Provides Business Update

THOMSON REUTERS
·
Mar 13

Savara Q4 EPS USD -0.13

THOMSON REUTERS
·
Mar 13

How FDA’s No-Advisory-Committee Path for MOLBREEVI Could Shape Savara (SVRA) Investors’ Outlook

Simply Wall St.
·
Mar 12

LifeSci Capital Keeps Their Buy Rating on Savara (SVRA)

TIPRANKS
·
Mar 10

Analysts Offer Insights on Healthcare Companies: Savara (SVRA), Codexis (CDXS) and Diamedica Therapeutics (DMAC)

TIPRANKS
·
Mar 09

Savara Inc. Publishes Corporate Presentation on Autoimmune PAP and MOLBREEVI Molgramostim Inhalation Solution

Reuters
·
Mar 07

Savara announces receipt of Day 74 Letter from FDA

TIPRANKS
·
Mar 07

BRIEF-Savara Provides Regulatory Update On The MOLBREEVI* Development Program In Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune Pap)

Reuters
·
Mar 07

Savara Inc - on Track to Submit Maa to UK Mhra by End of Q1 2026

THOMSON REUTERS
·
Mar 07

Savara Inc - Pdufa Target Action Date for Molbreevi Set for August 22, 2026

THOMSON REUTERS
·
Mar 07

Savara - Day 74 Letter Received From U.S. Food and Drug Administration Indicated Agency Has No Plans to Convene Advisory Committee

THOMSON REUTERS
·
Mar 07

Savara Provides Regulatory Update on the Molbreevi* Development Program in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune Pap)

THOMSON REUTERS
·
Mar 07

Savara says FDA plans no advisory panel for MOLBREEVI as review continues toward Aug. 22, 2026 PDUFA date

Reuters
·
Mar 07