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SVRA Overview

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$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
5.620
Open
5.620
VWAP
5.49
Vol
102.32K
Mkt Cap
1.14B
Low
5.410
Amount
562.08K
EV/EBITDA(TTM)
--
Total Shares
203.47M
EV
1.05B
EV/OCF(TTM)
--
P/S(TTM)
--
Savara Inc. is a clinical-stage biopharmaceutical company. The Company is focused on rare respiratory diseases. The Company’s lead program, molgramostim inhalation solution (MOLBREEVI or molgramostim), is an inhaled biologic, specifically an inhaled granulocyte-macrophage colony-stimulating factor (GM-CSF) in Phase III development for autoimmune pulmonary alveolar proteinosis (aPAP). MOLBREEVI is an inhaled formulation of recombinant human GM-CSF and is being developed for the treatment of aPAP. MOLBREEVI is administered once daily by inhalation via a high efficiency nebulizer, the eFlow Nebulizer System (PARI Pharma GmbH). Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by the accumulation of surfactant in the alveoli (or air sacs) of the lungs. The Company is engaged in the advancement of the MOLBREEVI aPAP program and the Phase III IMPALA-2 clinical trial and outsourcing capital-intensive operations.
Show More

Events Timeline

(ET)
2026-03-06
16:20:00
Savara Receives Day 74 Letter from FDA, MOLBREEVI Application Under Ongoing Review
select
2026-02-20 (ET)
2026-02-20
16:30:00
Savara Receives FDA Priority Review for Molbreevi
select
2026-02-20
16:20:00
Savara Receives FDA Priority Review for Molbreevi
select
2025-12-22 (ET)
2025-12-22
08:40:00
Savara Resubmits Molbreevi BLA to FDA, Requests Priority Review
select
2025-12-11 (ET)
2025-12-11
08:20:00
Savara Receives Notification from EPO for Molbreevi Patent Application
select
2025-12-02 (ET)
2025-12-02
14:30:00
Savara Shares Drop 2% to $5.73 Amid M&A Rumors
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2025-12-02
08:41:00
Savara and Pari Jointly Obtain Patent for Molbreevi Delivery System
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News

Newsfilter
9.0
03-06Newsfilter
Savara Receives FDA Day 74 Letter, MOLBREEVI Progressing Smoothly
  • FDA Review Progress: Savara has received a Day 74 Letter from the FDA indicating that no Advisory Committee meeting is planned for the MOLBREEVI Biologics License Application (BLA), with ongoing review expected to conclude by the PDUFA target action date of August 22, 2026, laying a solid foundation for market entry.
  • EMA Application Submission: The company has submitted the Marketing Authorization Application (MAA) for MOLBREEVI to the European Medicines Agency (EMA) and is on track to submit to the U.K.'s Medicines and Healthcare Products Regulatory Agency (MHRA) by the end of Q1 2026, further advancing its European market strategy.
  • Therapeutic Potential: MOLBREEVI is positioned as a first-in-class treatment for autoimmune pulmonary alveolar proteinosis (PAP), a rare disease with no approved therapies in the U.S. and Europe, which could fill a significant market gap and meet urgent patient needs if approved.
  • Regulatory Recognition: MOLBREEVI has received Fast Track and Breakthrough Therapy Designations from the FDA, as well as Orphan Drug Designation from both the FDA and EMA, highlighting regulatory confidence in its potential efficacy, which may expedite its market launch and enhance competitive positioning.
moomoo
9.0
03-06moomoo
SAVARA INC AIMS TO FILE MAA WITH UK MHRA BY END OF Q1 2026
  • Project Submission Timeline: Savara Inc. is on track to submit a New Drug Application (NDA) for its treatment, MaA, to the UK Medicines and Healthcare products Regulatory Agency (MHRA) by the end of the first quarter of 2026.

  • Regulatory Focus: The submission is part of Savara's ongoing efforts to gain regulatory approval for MaA, which is aimed at addressing specific health needs in the market.

stocktwits
9.0
02-21stocktwits
Savara Seeks FDA Approval for Molbreevi to Treat Rare Lung Disease
  • FDA Approval Progress: Savara Inc. has submitted an application for its experimental therapy Molbreevi, with the FDA expected to decide by August 22, 2026, indicating the drug's potential in treating autoimmune pulmonary alveolar proteinosis and possibly significantly improving patient quality of life.
  • Fast Track Designation: Molbreevi has received FDA's fast track, breakthrough therapy, and orphan drug designations, which not only expedite the approval process but also enhance investor confidence in the drug's market prospects, leading to a more than 3% rise in Savara's stock in after-hours trading.
  • International Application Plans: Savara plans to submit applications to the European Medicines Agency (EMA) and the UK's Medicines and Healthcare Products Regulatory Agency (MHRA) by the end of Q1 2026, demonstrating the company's strategic intent to promote Molbreevi globally and expand market opportunities.
  • Market Sentiment Shift: Retail sentiment around SVRA on Stocktwits has shifted from 'neutral' to 'bullish' over the past 24 hours, with message volume remaining high, reflecting investor optimism about the drug, as SVRA stock has more than doubled in the past 12 months, indicating strong market performance.
seekingalpha
9.0
02-20seekingalpha
FDA Grants Priority Review for Savara's Molbreevi BLA Resubmission
  • FDA Review Progress: The U.S. FDA will review Savara's resubmitted BLA for Molbreevi (molgramostim inhalation solution) with priority status, expected to make a decision by August 22, which accelerates the drug's market entry for treating rare lung diseases.
  • Drug Background: Molbreevi is a recombinant human granulocyte-macrophage colony-stimulating factor targeting autoimmune pulmonary alveolar proteinosis, and if approved, it will provide a new treatment option for patients, filling a significant market gap.
  • International Application Plans: Savara intends to submit applications to the European Medicines Agency and the UK's Medicines and Healthcare Products Regulatory Agency by the end of Q1, demonstrating its strategic intent for global market expansion and enhancing its competitiveness internationally.
  • Market Reaction: Savara's shares rose approximately 4.5% in after-hours trading on Friday, reflecting investor optimism regarding the FDA's priority review, which may indicate a positive outlook for the drug's future prospects.
Businesswire
9.0
02-20Businesswire
Savara Receives FDA Priority Review for MOLBREEVI BLA Submission
  • FDA Priority Review: Savara announced that the FDA has filed for Priority Review of the BLA for MOLBREEVI, with a PDUFA action date set for August 22, 2026, marking a significant milestone in the treatment of autoimmune pulmonary alveolar proteinosis and potentially offering new options for patients.
  • Clinical Data Support: CEO Matt Pauls stated that the substantial data in the application demonstrates that MOLBREEVI improves pulmonary gas transfer and quality of life, which not only enhances the company's reputation in the biopharmaceutical sector but also may drive growth in its market share.
  • Multiple Drug Designations: In addition to Priority Review, MOLBREEVI has received Orphan Drug Designation from both the FDA and EMA, as well as Innovation Passport and Promising Innovative Medicine designations from the UK's MHRA, indicating the drug's potential in treating rare diseases and further strengthening Savara's competitive position.
  • Strategic Implications: The development of MOLBREEVI is not only Savara's lead program but could also become the first approved therapy for autoimmune PAP in the U.S. and Europe, with successful commercialization significantly enhancing the company's revenue potential and industry standing.
Newsfilter
9.0
02-20Newsfilter
Savara Receives Priority Review for MOLBREEVI, Potential First Therapy for Autoimmune PAP
  • Priority Review Granted: The FDA has granted Priority Review for Savara's MOLBREEVI application, with a PDUFA action date set for August 22, 2026, marking a significant milestone for the company in the autoimmune PAP treatment space, which could greatly enhance patient quality of life if approved.
  • European Application Plans: Savara plans to submit Marketing Authorization Applications (MAAs) for MOLBREEVI to the European Medicines Agency (EMA) and the UK's Medicines and Healthcare Products Regulatory Agency (MHRA) by the end of Q1 2026, further expanding its international market presence and potentially generating new revenue streams.
  • Unique Treatment Potential: MOLBREEVI is poised to become the first approved therapy for autoimmune PAP in both the U.S. and Europe, filling a critical market gap and addressing the urgent need for effective treatments, thereby enhancing Savara's competitive position in the biopharmaceutical industry.
  • Clinical Data Support: Savara asserts that the application includes a substantial body of data demonstrating MOLBREEVI's ability to improve pulmonary gas transfer and clinical symptoms, which not only bolsters FDA confidence but also lays a solid foundation for future market promotion.
Wall Street analysts forecast SVRA stock price to rise
6 Analyst Rating
Wall Street analysts forecast SVRA stock price to rise
6 Buy
0 Hold
0 Sell
Strong Buy
Current: 0.000
sliders
Low
9.00
Averages
10.17
High
11.00
Current: 0.000
sliders
Low
9.00
Averages
10.17
High
11.00
H.C. Wainwright
Andrew Fein
Buy
maintain
$8 -> $10
AI Analysis
2025-12-23
Reason
H.C. Wainwright
Andrew Fein
Price Target
$8 -> $10
AI Analysis
2025-12-23
maintain
Buy
Reason
H.C. Wainwright analyst Andrew Fein raised the firm's price target on Savara to $10 from $8 and keeps a Buy rating on the shares. The company resubmitted the application for Molbreevi with Fujifilm Diosynth as its drug substance manufacturer, the analyst tells investors in a research note. The firm believes Savara is increasingly well positioned ahead of a potential Molbreevi launch.
Oppenheimer
Oppenheimer
Outperform
maintain
$8 -> $9
2025-11-14
Reason
Oppenheimer
Oppenheimer
Price Target
$8 -> $9
2025-11-14
maintain
Outperform
Reason
Oppenheimer raised the firm's price target on Savara to $9 from $8 and keeps an Outperform rating on the shares. Ahead of December 2025 BLA submission for MOLBREEVI, the firm continues to see a more than $1B opportunity for MOLBREEVI in aPAP following recent updated claims data giving line of sight to at least 1,000 patients by launch with 750 already identified.
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Valuation Metrics

The current forward P/E ratio for Savara Inc (SVRA.O) is -13.37, compared to its 5-year average forward P/E of -7.18. For a more detailed relative valuation and DCF analysis to assess Savara Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-7.18
Current PE
-13.37
Overvalued PE
-4.13
Undervalued PE
-10.23

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
-0.38
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
4.20
Undervalued EV/EBITDA
-4.96

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PS
24.96
Current PS
537.26
Overvalued PS
132.03
Undervalued PS
-82.11

Financials

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Whales Holding SVRA

F
Frazier Life Sciences Management, LP
Holding
SVRA
+9.72%
3M Return
V
Vestal Point Capital, LP
Holding
SVRA
+6.94%
3M Return
V
VR Management, LLC
Holding
SVRA
+6.00%
3M Return
T
TCG Crossover Management, LLC
Holding
SVRA
+1.37%
3M Return
D
Deerfield Management Company, L.P.
Holding
SVRA
+0.18%
3M Return
N
New Enterprise Associates, Inc.
Holding
SVRA
-2.25%
3M Return

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Frequently Asked Questions

What is Savara Inc (SVRA) stock price today?

The current price of SVRA is 5.45 USD — it has decreased -2.85

What is Savara Inc (SVRA)'s business?

Savara Inc. is a clinical-stage biopharmaceutical company. The Company is focused on rare respiratory diseases. The Company’s lead program, molgramostim inhalation solution (MOLBREEVI or molgramostim), is an inhaled biologic, specifically an inhaled granulocyte-macrophage colony-stimulating factor (GM-CSF) in Phase III development for autoimmune pulmonary alveolar proteinosis (aPAP). MOLBREEVI is an inhaled formulation of recombinant human GM-CSF and is being developed for the treatment of aPAP. MOLBREEVI is administered once daily by inhalation via a high efficiency nebulizer, the eFlow Nebulizer System (PARI Pharma GmbH). Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by the accumulation of surfactant in the alveoli (or air sacs) of the lungs. The Company is engaged in the advancement of the MOLBREEVI aPAP program and the Phase III IMPALA-2 clinical trial and outsourcing capital-intensive operations.

What is the price predicton of SVRA Stock?

Wall Street analysts forecast SVRA stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for SVRA is10.17 USD with a low forecast of 9.00 USD and a high forecast of 11.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Savara Inc (SVRA)'s revenue for the last quarter?

Savara Inc revenue for the last quarter amounts to 0.00 USD, decreased

What is Savara Inc (SVRA)'s earnings per share (EPS) for the last quarter?

Savara Inc. EPS for the last quarter amounts to -0.14 USD, increased 27.27

How many employees does Savara Inc (SVRA). have?

Savara Inc (SVRA) has 59 emplpoyees as of March 11 2026.

What is Savara Inc (SVRA) market cap?

Today SVRA has the market capitalization of 1.14B USD.