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SPRO Overview

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Intellectia

Loading chart...

High
2.280
Open
2.230
VWAP
2.21
Vol
629.52K
Mkt Cap
127.38M
Low
2.150
Amount
1.39M
EV/EBITDA(TTM)
5.03
Total Shares
57.90M
EV
71.25M
EV/OCF(TTM)
9.84
P/S(TTM)
2.14
Spero Therapeutics, Inc. is a clinical-stage biopharmaceutical company. The Company is focused on identifying and developing novel treatments for rare diseases and diseases caused by multi-drug resistant (MDR) bacterial infections with unmet need. Its product candidate SPR720 is an investigational, chemically stable phosphate ester prodrug that is converted in vivo to SPR719 for the treatment of nontuberculous mycobacterial (NTM) pulmonary disease. Its clinical stage product candidate, tebipenem HBr is an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTIs) including acute pyelonephritis (AP) to help patients potentially reduce duration of in-patient therapy.
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Events Timeline

(ET)
2026-06-17
11:30:00
GSK and Spero Therapeutics Get FDA Approval for Utebzi Antibiotic
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2025-12-19 (ET)
2025-12-19
08:20:00
Spero Therapeutics Receives $25 Million Milestone Payment Triggered by GSK's NDA Submission
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2025-11-28 (ET)
2025-11-28
08:08:43
Spero Therapeutics Reveals Inducement Grant in Accordance with Nasdaq Listing Regulations
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2025-10-21 (ET)
2025-10-21
05:46:08
Spero Therapeutics and GSK Reveal Efficacy and Safety Outcomes of PIVOT-PO Trial
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2025-05-28 (ET)
2025-05-28
07:17:32
GSK reports PIVOT-PO study for tebipenem HBr stopped early for efficacy
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2025-05-28
07:05:59
Spero Therapeutics, GSK announce Phase 3 PIVOT-PO trial met primary endpoint
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2025-04-28 (ET)
2025-04-28
16:08:20
Spero Therapeutics appoints Esther Rajavelu will serve as CEO
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2025-03-27 (ET)
2025-03-27
16:15:34
Spero Therapeutics reports Q4 EPS (38c), consensus (31c)
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News

Globenewswire
5.0
06-29Globenewswire
Kailera Appoints New Chief Corporate Affairs Officer
  • Executive Appointment: Kailera Therapeutics has appointed Kathleen Tregoning as Chief Corporate Affairs Officer to advance its obesity clinical trials and navigate the rapidly evolving treatment landscape, thereby enhancing the company's leadership position in obesity care.
  • Extensive Experience: Tregoning brings over 20 years of global corporate affairs experience, having held executive roles in biopharmaceutical companies, particularly her successful tenures at Cerevel Therapeutics and Sanofi, which will provide Kailera with strategic insights to navigate complex policy and regulatory environments.
  • Pipeline Development: Kailera is focused on developing multiple GLP-1-based therapeutic options and is advancing four clinical-stage candidates, including the global Phase 3 trial of KAI-9531, which is expected to offer significant weight loss benefits for obesity patients.
  • Market Outlook: As obesity becomes an increasingly pressing issue, Kailera's innovative product portfolio aims to meet the needs of patients and healthcare systems, and Tregoning's addition is expected to enhance the company's competitiveness in this dynamic market, driving its long-term growth strategy.
NASDAQ.COM
8.5
06-19NASDAQ.COM
Biotech Sector Sees FDA Approvals and Layoffs
  • FDA Drug Approval: Spero Therapeutics and GSK announced FDA approval for Utebzi, the first oral carbapenem for complicated urinary tract infections, marking a significant advancement in treatment options for adults with limited choices, which is expected to enhance market share.
  • Expanded Injectable Indication: AbbVie's SKINVIVE received FDA approval to improve neck lines in adults over 21, with pivotal studies showing nearly 75% of patients achieving significant improvement at one month, further solidifying AbbVie's leadership in the aesthetics market.
  • Strategic Acquisition: Biogen agreed to acquire RayThera for up to $1 billion to expand its immunology portfolio, with the transaction expected to close in Q3 2026, enhancing Biogen's competitive position in the immunotherapy space.
  • Layoff Plans: Neumora Therapeutics announced a 35% workforce reduction to save $10 million annually, reflecting strategic adjustments following the failure to meet primary endpoints in clinical trials, aimed at extending cash runway.
NASDAQ.COM
9.0
06-18NASDAQ.COM
GSK and Spero Gain FDA Approval for New Antibiotic
  • FDA Approval: GSK and Spero Therapeutics announced that the FDA has approved Utebzi as the first oral carbapenem antibiotic for adults with complicated urinary tract infections, marking a significant breakthrough in treatment options.
  • Successful Clinical Trials: Utebzi demonstrated non-inferiority to intravenous therapy in the PIVOT-PO Phase 3 trial, meeting the primary efficacy endpoint, which is expected to significantly enhance patient treatment experiences and reduce reliance on hospital care.
  • High Market Demand: With over 3 million cases of complicated urinary tract infections annually in the U.S. and a treatment failure rate of up to 34%, the introduction of Utebzi is anticipated to decrease dependence on intravenous carbapenems, thereby lowering healthcare costs and improving patient quality of life.
  • Strategic Implications: GSK's CSO Tony Wood emphasized that the approval of Utebzi is particularly crucial amid rising antibiotic resistance, as it supports innovative infection treatment and enhances patient treatment options.
Newsfilter
8.5
06-17Newsfilter
First Oral Carbapenem Antibiotic Approved in the US
  • FDA Approval: The US FDA has approved Utebzi, the first oral carbapenem antibiotic for treating complicated urinary tract infections (cUTIs), marking a new treatment option that is expected to improve patient quality of life and reduce reliance on intravenous therapy.
  • Clinical Trial Success: The PIVOT-PO trial demonstrated that Utebzi's efficacy is comparable to intravenous imipenem-cilastatin, with success rates of 58.5% and 60.2% respectively, providing patients with an effective oral alternative that may decrease hospital resource utilization.
  • Significant Market Demand: With over 3 million cUTI cases annually in the US and up to 34% of patients facing resistant infections, the introduction of Utebzi is poised to alleviate this healthcare burden and reduce the over $6 billion in associated healthcare costs each year.
  • Strategic Partnership Outcome: This approval is a result of the collaboration between GSK and Spero Therapeutics, which will facilitate the market launch of Utebzi, anticipated to be available to US patients by the end of 2026, further enhancing GSK's competitive position in the anti-infectives sector.
Newsfilter
8.5
06-17Newsfilter
First Oral Carbapenem Antibiotic Approved in the US
  • FDA Approval: The US FDA has approved Utebzi, the first oral carbapenem antibiotic developed by Spero Therapeutics and GSK for treating complicated urinary tract infections, marking a significant advancement in antibiotic treatment options and expected to enhance patient care.
  • Clinical Trial Results: The PIVOT-PO trial demonstrated non-inferiority of oral Tebipenem pivoxil compared to intravenous Imipenem-cilastatin in treating complicated UTIs, with success rates of 58.5% and 60.2% respectively, providing a new therapeutic alternative for patients.
  • Significant Market Demand: With over 3 million cases of complicated UTIs annually in the US and approximately 34% of patients facing treatment failure, the introduction of Utebzi is anticipated to significantly reduce hospital resource utilization and alleviate healthcare costs, potentially saving over $6 billion per year.
  • Strategic Collaboration Outcome: This approval reflects the successful partnership between GSK and Spero Therapeutics, which not only advanced the development of this new drug but also addresses the urgent need for new treatment options in the face of rising antibiotic resistance globally.
seekingalpha
9.0
06-17seekingalpha
GSK and Spero's Utebzi Approved by FDA for UTIs
  • Drug Approval: The US FDA has approved Utebzi (tebipenem pivoxil), developed by GSK and Spero Therapeutics, marking it as the first oral carbapenem therapy for complicated urinary tract infections, representing a significant breakthrough in treatment options.
  • Clinical Trial Results: A double-blind, randomized non-inferiority trial involving approximately 1,700 hospitalized patients demonstrated that the oral administration of Utebzi 600 mg every six hours is as effective as the intravenous imipenem-cilastatin 500 mg every six hours, further validating its clinical application potential.
  • Exclusive License: GSK has secured an exclusive license for Utebzi in all markets except Japan and certain parts of Asia, which strategically positions GSK to expand its market share in the global anti-infective drug sector.
  • Market Outlook: With the launch of Utebzi, GSK's competitiveness in the treatment of complicated urinary tract infections is expected to significantly enhance, likely driving future revenue growth and strengthening its leadership position in the anti-infective drug market.
Wall Street analysts forecast SPRO stock price to rise
2 Analyst Rating
Wall Street analysts forecast SPRO stock price to rise
0 Buy
2 Hold
0 Sell
Hold
Current: 0.000
sliders
Low
4.00
Averages
4.00
High
4.00
Current: 0.000
sliders
Low
4.00
Averages
4.00
High
4.00
No data

No data

Valuation Metrics

The current forward P/E ratio for Spero Therapeutics Inc (SPRO.O) is 0.00, compared to its 5-year average forward P/E of -1.92. For a more detailed relative valuation and DCF analysis to assess Spero Therapeutics 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
-1.92
Current PE
0.00
Overvalued PE
0.18
Undervalued PE
-4.01

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
-0.83
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
0.95
Undervalued EV/EBITDA
-2.60

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
10.63
Current PS
0.00
Overvalued PS
25.56
Undervalued PS
-4.29

Financials

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Frequently Asked Questions

What is Spero Therapeutics Inc (SPRO) stock price today?

The current price of SPRO is 2.2 USD — it has decreased -0.9

What is Spero Therapeutics Inc (SPRO)'s business?

Spero Therapeutics, Inc. is a clinical-stage biopharmaceutical company. The Company is focused on identifying and developing novel treatments for rare diseases and diseases caused by multi-drug resistant (MDR) bacterial infections with unmet need. Its product candidate SPR720 is an investigational, chemically stable phosphate ester prodrug that is converted in vivo to SPR719 for the treatment of nontuberculous mycobacterial (NTM) pulmonary disease. Its clinical stage product candidate, tebipenem HBr is an investigational oral carbapenem antibiotic being developed for the treatment of complicated urinary tract infections (cUTIs) including acute pyelonephritis (AP) to help patients potentially reduce duration of in-patient therapy.

What is the price predicton of SPRO Stock?

Wall Street analysts forecast SPRO stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for SPRO is4.00 USD with a low forecast of 4.00 USD and a high forecast of 4.00 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 Spero Therapeutics Inc (SPRO)'s revenue for the last quarter?

Spero Therapeutics Inc revenue for the last quarter amounts to 258.00K USD, decreased -95.61

What is Spero Therapeutics Inc (SPRO)'s earnings per share (EPS) for the last quarter?

Spero Therapeutics Inc. EPS for the last quarter amounts to -0.13 USD, decreased -48.00

How many employees does Spero Therapeutics Inc (SPRO). have?

Spero Therapeutics Inc (SPRO) has 25 emplpoyees as of July 05 2026.

What is Spero Therapeutics Inc (SPRO) market cap?

Today SPRO has the market capitalization of 127.38M USD.