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Spero Therapeutics

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uuid0002lvs

Namestring
Spero Therapeutics
Legal namestring
Spero Therapeutics, Inc.
Company typeenum
Public
Founded yearint
2013
Descriptiontext

Spero Therapeutics, Inc. is a Cambridge, Massachusetts-based clinical-stage biopharmaceutical company founded in 2013 and listed on NASDAQ (ticker SPRO) since November 2017, focused on developing therapeutics for multidrug-resistant (MDR) bacterial infections and rare infectious diseases. The company's lead asset, Utebzi (tebipenem pivoxil hydrobromide, formerly SPR994), is an oral carbapenem antibiotic that received FDA approval on June 17, 2026 for the treatment of complicated urinary tract infections (cUTIs) including pyelonephritis in adults, becoming the first and only oral carbapenem available in the U.S. The Phase 3 PIVOT-PO trial showed 58.5% clinical success versus 60.2% for IV imipenem-cilastatin. The pipeline additionally includes SPR206, an IV polymyxin derivative for MDR infections that is licensed to Pfizer for development outside the U.S. and Asian territories, and SPR720, an oral candidate for non-tuberculous mycobacterial pulmonary disease with Phase 1 data published.

Spero generates revenue primarily through licensing and collaboration economics rather than direct product sales. In September 2022, GSK acquired near-global rights to tebipenem HBr in exchange for a $66 million upfront payment, up to $750 million in potential milestones, tiered royalties on net sales, and a $9 million equity investment in Spero. Pfizer's 2021 deal for SPR206 provided $40 million in equity and licensing economics for ex-U.S./Asian territories. HealthCare Royalty Partners provided $125 million in revenue-interest financing in 2021, and BARDA's pediatric development contract has a potential value of up to $59.7 million in non-dilutive government funding. FY2025 revenue totaled $66.8 million, driven largely by collaboration milestone and grant recognition including a $25 million milestone from GSK triggered by NDA resubmission in December 2025.

The company operates through a small team of 11-50 employees and runs a partner-driven commercialization model: GSK leads global Utebzi commercialization via established hospital formularies, retail pharmacy networks, and specialty distributors, while Pfizer owns ex-U.S. development rights for SPR206. Headquartered at 675 Massachusetts Avenue in Cambridge, MA, Spero has been recognized multiple times as one of Boston's Best Places to Work by the Boston Business Journal (2020, 2021, 2024) and maintains $56.1 million in cash and equivalents as of Q1 2026 with an operating runway extending into 2028.

Short descriptiontext

Spero Therapeutics is a Cambridge, MA-based biopharmaceutical company developing oral carbapenem antibiotics and other therapeutics for multidrug-resistant bacterial infections, with its lead product Utebzi (tebipenem pivoxil) FDA-approved in June 2026 for complicated urinary tract infections.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersCambridge, United States
HQ citystring
Cambridge
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
antibiotic drug development, multidrug-resistant infection therapies, oral carbapenem antibiotics, complicated urinary tract infection treatment, rare disease pharmaceuticals
Industry3 codes
PRIMARYHLAIAAAG
Infectious Disease & Antimicrobials Pharmaceuticals
Healthcare & Life Sciences/Pharmaceuticals/Branded (Innovator) Pharmaceuticals
SECONDARYHLAIACAF
Pulmonology & Allergy Specialty Pharmaceuticals
SECONDARYHLAIACAH
Nephrology & Urology Specialty Pharmaceuticals
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Infectious Disease Pharmaceuticals
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model4 records
1Licensing Royalties from GSK
TypeLicensing Royalties
Description

GSK pays Spero royalties on net sales of Utebzi (tebipenem pivoxil). Royalty structure rewards meaningful cash flow above $750M in annual net sales. Potential royalties of approximately $50 million annually with upside exceeding $100 million if blockbuster status achieved.

biospace.com
2Licensing Revenue from Pfizer
TypeLicensing Royalties
Description

Pfizer licensed SPR206 for development outside U.S. and Asian territories, with Spero receiving upfront payment and potential milestone payments.

pfizer.com
3BARDA Grant Funding
TypeProfessional Services
Description

Biomedical Advanced Research and Development Authority provides funding support for tebipenem pediatric development, totaling up to $59.7 million potential contract value.

globenewswire.com
4Revenue Interest Financing
TypeLicensing Royalties
Description

HealthCare Royalty Partners agreement providing upfront funding with potential milestones and royalties based on future revenue from medical products.

biospace.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Infrastructure
Pricing details1 tier
1Prescription pharmaceutical product for complicated urinary tract infections
ModelOtherBilling cadencePay-as-you-go
Notes

Pricing not yet publicly disclosed as of FDA approval date June 2026. Market opportunity addresses over 3 million annual cUTI cases representing $6 billion in healthcare costs.

m.au.investing.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Spero Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of antibacterial and anti-infective medicines. Its lead commercial product is Utebzi (tebipenem pivoxil hydrobromide), the first and only oral carbapenem antibiotic approved in the U.S. for complicated urinary tract infections (cUTIs) including pyelonephritis in adults. The pipeline includes SPR206 (a polymyxin derivative for multi-drug resistant bacterial infections, licensed to Pfizer) and SPR720 (an oral agent for non-tuberculous mycobacterial pulmonary disease).

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 58.5% overall success rate vs 60.2% for IV imipenem-cilastatin in PIVOT-PO Phase 3 trial
+3 more records
Product overview1 text field

Spero Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of investigational medicines targeting rare diseases and multidrug-resistant (MDR) bacterial infections. The company's lead product is Utebzi (tebipenem pivoxil hydrobromide), an FDA-approved oral carbapenem antibiotic for complicated urinary tract infections - the first and only oral carbapenem available in the US. The pipeline includes SPR206 (licensed to Pfizer for MDR bacterial infections) and SPR720 (in development for non-tuberculous mycobacterial pulmonary disease). The company operates through partnerships with major pharmaceutical companies including GSK (for tebipenem HBr) and Pfizer (for SPR206), with funding support from government agencies like BARDA.

Product and service3 records
1Utebzi (tebipenem pivoxil hydrobromide)
CategoryApproved Drug Product
Description

FDA-approved oral carbapenem antibiotic for treating complicated urinary tract infections (cUTIs) including pyelonephritis in adults. The first and only oral carbapenem approved in the U.S., developed to help patients avoid hospitalizations or transition home after IV therapy. Commercialized globally (outside Japan and certain Asian territories) by GSK under exclusive license.

2SPR206
CategoryLicensed Drug Candidate
Description

Investigational intravenous polymyxin derivative drug candidate for the treatment of multi-drug resistant bacterial infections. Licensed to Pfizer for development and commercialization outside of U.S. and Asian territories under a 2021 agreement that included a $40 million equity investment.

3SPR720
CategoryClinical Stage Asset
Description

Investigational oral drug candidate for the treatment of non-tuberculous mycobacterial (NTM) pulmonary disease. Phase 1 clinical trial results have been published. Remains in clinical-stage development.

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierFlagshipTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2022-09-22
Description

Exclusive global licensing agreement for tebipenem HBr (Utebzi). GSK received rights to commercialize outside Japan and certain Asian territories. Spero received $66 million upfront, potential milestones up to $750 million, tiered royalties, and GSK purchased $9 million in Spero shares. FDA approved Utebzi on June 17, 2026 for cUTI in adults. GSK assumes NDA sponsorship and commercialization responsibilities.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2021-06-30
Description

$40 million equity investment and licensing agreement for SPR206, a drug candidate for multi-drug resistant bacterial infections. Pfizer purchased shares and obtained rights to develop and commercialize SPR206 outside U.S. and Asian territories. Spero uses funds to support clinical pipeline.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Strategic partner with logo displayed on Spero Therapeutics partnerships page; specific collaboration details not detailed in available sources.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Strategic partner with logo displayed on Spero Therapeutics partnerships page; specific collaboration details not detailed in available sources.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Melinta Therapeutics is a specialty antibiotics company commercializing drugs for serious bacterial infections, directly comparable as a focused anti-infective pharma with both marketed and development-stage carbapenem/quinolone assets.

TypeBroad incumbent
Description

GSK is Spero's primary commercialization partner (Utebzi global licensee) and a broad incumbent with extensive infectious disease and antibiotics heritage, comparable as the counterparty controlling Utebzi's commercial destiny.

TypeDirect peer
Description

Tetraphase developed eravacycline (Xerava), an IV antibiotic approved for complicated intra-abdominal infections, and was acquired by La Jolla Pharmaceutical — a relevant precedent for a small-cap anti-infective with a single approved asset.

TypeBroad incumbent
Description

Pfizer is both an Spero partner (SPR206 licensee, $40M equity investor) and a broad incumbent in the anti-infective space with established carbapenem franchises (meropenem) and large infectious disease R&D infrastructure that could compete in MDR infections.

TypeDirect peer
Description

Paratek Pharmaceuticals developed and commercialized omadacycline and tetracycline-class antibiotics, a comparable specialty anti-infective company that navigated similar FDA approval and partnership dynamics.

TypeDirect peer
Description

Iterum Therapeutics is developing oral antibiotics (sulopenem) for complicated urinary tract infections, directly competing with Spero's Utebzi in the same cUTI oral step-down market with similar patient population and prescriber base.

TypeDirect peer
Description

Nabriva Therapeutics develops antibiotics for community-acquired pneumonia and complicated UTIs, making it a direct peer in the specialty anti-infective space with similar regulatory and commercialization challenges.

TypeDirect peer
Description

Cidara Therapeutics develops anti-infectives including antivirals and antibacterial conjugates, comparable to Spero as a small clinical-stage biopharma focused on novel anti-infective modalities.

TypeEmerging player
Description

BioMarin is a rare-disease focused biopharma with a similar small-cap commercial-stage model — relevant as a comp for how a specialty pharma of Spero's size monetizes a single high-need therapy through partnership-driven commercialization.

TypeDirect peer
Description

Innoviva acquired Entasis Therapeutics and VenatoRx, both of which developed novel antibiotics for multi-drug resistant bacterial infections — directly comparable to Spero's SPR206 program targeting the same MDR Gram-negative market.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles11 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds16 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors21 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Spero Therapeutics

Infectious Disease Pharmaceuticalssperotherapeutics.com

Spero Therapeutics is a Cambridge, MA-based biopharmaceutical company developing oral carbapenem antibiotics and other therapeutics for multidrug-resistant bacterial infections, with its lead product Utebzi (tebipenem pivoxil) FDA-approved in June 2026 for complicated urinary tract infections.

What Spero Therapeutics does

Spero Therapeutics, Inc. is a Cambridge, Massachusetts-based clinical-stage biopharmaceutical company founded in 2013 and listed on NASDAQ (ticker SPRO) since November 2017, focused on developing therapeutics for multidrug-resistant (MDR) bacterial infections and rare infectious diseases. The company's lead asset, Utebzi (tebipenem pivoxil hydrobromide, formerly SPR994), is an oral carbapenem antibiotic that received FDA approval on June 17, 2026 for the treatment of complicated urinary tract infections (cUTIs) including pyelonephritis in adults, becoming the first and only oral carbapenem available in the U.S. The Phase 3 PIVOT-PO trial showed 58.5% clinical success versus 60.2% for IV imipenem-cilastatin. The pipeline additionally includes SPR206, an IV polymyxin derivative for MDR infections that is licensed to Pfizer for development outside the U.S. and Asian territories, and SPR720, an oral candidate for non-tuberculous mycobacterial pulmonary disease with Phase 1 data published.

Spero generates revenue primarily through licensing and collaboration economics rather than direct product sales. In September 2022, GSK acquired near-global rights to tebipenem HBr in exchange for a $66 million upfront payment, up to $750 million in potential milestones, tiered royalties on net sales, and a $9 million equity investment in Spero. Pfizer's 2021 deal for SPR206 provided $40 million in equity and licensing economics for ex-U.S./Asian territories. HealthCare Royalty Partners provided $125 million in revenue-interest financing in 2021, and BARDA's pediatric development contract has a potential value of up to $59.7 million in non-dilutive government funding. FY2025 revenue totaled $66.8 million, driven largely by collaboration milestone and grant recognition including a $25 million milestone from GSK triggered by NDA resubmission in December 2025.

The company operates through a small team of 11-50 employees and runs a partner-driven commercialization model: GSK leads global Utebzi commercialization via established hospital formularies, retail pharmacy networks, and specialty distributors, while Pfizer owns ex-U.S. development rights for SPR206. Headquartered at 675 Massachusetts Avenue in Cambridge, MA, Spero has been recognized multiple times as one of Boston's Best Places to Work by the Boston Business Journal (2020, 2021, 2024) and maintains $56.1 million in cash and equivalents as of Q1 2026 with an operating runway extending into 2028.

Spero Therapeutics firmographics

Firmographics
Name
Spero Therapeutics
Legal name
Spero Therapeutics, Inc.
Website
https://sperotherapeutics.com
Company type
Public
Founded year
2013
Operating status
Operating
Headcount range
11–50 employees
Short description
Spero Therapeutics is a Cambridge, MA-based biopharmaceutical company developing oral carbapenem antibiotics and other therapeutics for multidrug-resistant bacterial infections, with its lead product Utebzi (tebipenem pivoxil) FDA-approved in June 2026 for complicated urinary tract infections.
Ownership category
akta.pro rank

Spero Therapeutics industry classification

Industry
Product category
Infectious Disease Pharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Pharmaceutical Preparations (2834)
akta.pro industry
PRIMARYHLAIAAAG
Infectious Disease & Antimicrobials Pharmaceuticals
Healthcare & Life Sciences/Pharmaceuticals/Branded (Innovator) Pharmaceuticals
SECONDARYHLAIACAF
Pulmonology & Allergy Specialty Pharmaceuticals
SECONDARYHLAIACAH
Nephrology & Urology Specialty Pharmaceuticals

Keywords

  • Antibiotic drug development
  • Multidrug-resistant infection therapies
  • Oral carbapenem antibiotics
  • Complicated urinary tract infection treatment
  • Rare disease pharmaceuticals

Where Spero Therapeutics is headquartered

Location

Headquarters

HQ city
Cambridge
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Spero Therapeutics business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Infrastructure

Revenue model

  1. Licensing Royalties from GSK: GSK pays Spero royalties on net sales of Utebzi (tebipenem pivoxil). Royalty structure rewards meaningful cash flow above $750M in annual net sales. Potential royalties of approximately $50 million annually with upside exceeding $100 million if blockbuster status achieved.
  2. Licensing Revenue from Pfizer: Pfizer licensed SPR206 for development outside U.S. and Asian territories, with Spero receiving upfront payment and potential milestone payments.
  3. BARDA Grant Funding: Biomedical Advanced Research and Development Authority provides funding support for tebipenem pediatric development, totaling up to $59.7 million potential contract value.
  4. Revenue Interest Financing: HealthCare Royalty Partners agreement providing upfront funding with potential milestones and royalties based on future revenue from medical products.

Pricing tiers

ModelBillingPrice
OtherPay-as-you-goPrescription pharmaceutical product for complicated urinary tract infections

Go-to-market motion1 record

Distribution channels2 records

Marketing channels4 records

Spero Therapeutics product offering

Product offering

Core offering

Spero Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of antibacterial and anti-infective medicines. Its lead commercial product is Utebzi (tebipenem pivoxil hydrobromide), the first and only oral carbapenem antibiotic approved in the U.S. for complicated urinary tract infections (cUTIs) including pyelonephritis in adults. The pipeline includes SPR206 (a polymyxin derivative for multi-drug resistant bacterial infections, licensed to Pfizer) and SPR720 (an oral agent for non-tuberculous mycobacterial pulmonary disease).

Product overview

Spero Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of investigational medicines targeting rare diseases and multidrug-resistant (MDR) bacterial infections. The company's lead product is Utebzi (tebipenem pivoxil hydrobromide), an FDA-approved oral carbapenem antibiotic for complicated urinary tract infections - the first and only oral carbapenem available in the US. The pipeline includes SPR206 (licensed to Pfizer for MDR bacterial infections) and SPR720 (in development for non-tuberculous mycobacterial pulmonary disease). The company operates through partnerships with major pharmaceutical companies including GSK (for tebipenem HBr) and Pfizer (for SPR206), with funding support from government agencies like BARDA.

Differentiator

Problem solved

Functional benefit

Products and services

  • Utebzi (tebipenem pivoxil hydrobromide) FDA-approved oral carbapenem antibiotic for treating complicated urinary tract infections (cUTIs) including pyelonephritis in adults. The first and only oral carbapenem approved in the U.S., developed to help patients avoid hospitalizations or transition home after IV therapy. Commercialized globally (outside Japan and certain Asian territories) by GSK under exclusive license.
  • SPR206 Investigational intravenous polymyxin derivative drug candidate for the treatment of multi-drug resistant bacterial infections. Licensed to Pfizer for development and commercialization outside of U.S. and Asian territories under a 2021 agreement that included a $40 million equity investment.
  • SPR720 Investigational oral drug candidate for the treatment of non-tuberculous mycobacterial (NTM) pulmonary disease. Phase 1 clinical trial results have been published. Remains in clinical-stage development.

Quantifiable outcome

  • 58.5% overall success rate vs 60.2% for IV imipenem-cilastatin in PIVOT-PO Phase 3 trial
  • +3 more outcomes

Companies that use Spero Therapeutics

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles2 records

Spero Therapeutics technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Spero Therapeutics partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered flagship, core and minor.

  • GSK (GlaxoSmithKline)flagshipOEM/ Whitelabel/ Licensing Partner · 22 September 2022Exclusive global licensing agreement for tebipenem HBr (Utebzi). GSK received rights to commercialize outside Japan and certain Asian territories. Spero received $66 million upfront, potential milestones up to $750 million, tiered royalties, and GSK purchased $9 million in Spero shares. FDA approved Utebzi on June 17, 2026 for cUTI in adults. GSK assumes NDA sponsorship and commercialization responsibilities.
  • Pfizer Inc.coreOEM/ Whitelabel/ Licensing Partner · 30 June 2021$40 million equity investment and licensing agreement for SPR206, a drug candidate for multi-drug resistant bacterial infections. Pfizer purchased shares and obtained rights to develop and commercialize SPR206 outside U.S. and Asian territories. Spero uses funds to support clinical pipeline.
  • Meiji Seika PharmaminorStrategic or Co-development PartnerStrategic partner with logo displayed on Spero Therapeutics partnerships page; specific collaboration details not detailed in available sources.
  • Vertex PharmaceuticalsminorStrategic or Co-development PartnerStrategic partner with logo displayed on Spero Therapeutics partnerships page; specific collaboration details not detailed in available sources.

Scale indicators11 records

Recent moves7 records

Expansion highlights5 records

Spero Therapeutics competitors and assessment

Company assessment

Direct peers

  • Melinta Therapeutics: Melinta Therapeutics is a specialty antibiotics company commercializing drugs for serious bacterial infections, directly comparable as a focused anti-infective pharma with both marketed and development-stage carbapenem/quinolone assets.
  • Tetraphase Biosciences: Tetraphase developed eravacycline (Xerava), an IV antibiotic approved for complicated intra-abdominal infections, and was acquired by La Jolla Pharmaceutical — a relevant precedent for a small-cap anti-infective with a single approved asset.
  • Paratek Pharmaceuticals: Paratek Pharmaceuticals developed and commercialized omadacycline and tetracycline-class antibiotics, a comparable specialty anti-infective company that navigated similar FDA approval and partnership dynamics.
  • Iterum Therapeutics: Iterum Therapeutics is developing oral antibiotics (sulopenem) for complicated urinary tract infections, directly competing with Spero's Utebzi in the same cUTI oral step-down market with similar patient population and prescriber base.
  • Nabriva Therapeutics: Nabriva Therapeutics develops antibiotics for community-acquired pneumonia and complicated UTIs, making it a direct peer in the specialty anti-infective space with similar regulatory and commercialization challenges.
  • Cidara Therapeutics: Cidara Therapeutics develops anti-infectives including antivirals and antibacterial conjugates, comparable to Spero as a small clinical-stage biopharma focused on novel anti-infective modalities.
  • Innoviva Specialty Therapeutics (formerly Entasis/VenatoRx): Innoviva acquired Entasis Therapeutics and VenatoRx, both of which developed novel antibiotics for multi-drug resistant bacterial infections — directly comparable to Spero's SPR206 program targeting the same MDR Gram-negative market.

Broad incumbents

  • GSK (GlaxoSmithKline): GSK is Spero's primary commercialization partner (Utebzi global licensee) and a broad incumbent with extensive infectious disease and antibiotics heritage, comparable as the counterparty controlling Utebzi's commercial destiny.
  • Pfizer Inc. Pfizer is both an Spero partner (SPR206 licensee, $40M equity investor) and a broad incumbent in the anti-infective space with established carbapenem franchises (meropenem) and large infectious disease R&D infrastructure that could compete in MDR infections.

Emerging players

  • BioMarin Pharmaceutical: BioMarin is a rare-disease focused biopharma with a similar small-cap commercial-stage model — relevant as a comp for how a specialty pharma of Spero's size monetizes a single high-need therapy through partnership-driven commercialization.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Spero Therapeutics social profiles

Digital presence

Spero Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Spero Therapeutics leadership team

Management profile

Number of profiles

Profiles11 records

Spero Therapeutics funding detail

Funding detail

Funding overview

Funding rounds16 records

Investors21 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Spero Therapeutics M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Spero Therapeutics

What does Spero Therapeutics do?

Spero Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of antibacterial and anti-infective medicines. Its lead commercial product is Utebzi (tebipenem pivoxil hydrobromide), the first and only oral carbapenem antibiotic approved in the U.S. for complicated urinary tract infections (cUTIs) including pyelonephritis in adults. The pipeline includes SPR206 (a polymyxin derivative for multi-drug resistant bacterial infections, licensed to Pfizer) and SPR720 (an oral agent for non-tuberculous mycobacterial pulmonary disease).

Is Spero Therapeutics a public or private company?

Spero Therapeutics is a public company. It is classified as public and is currently operating.

When was Spero Therapeutics founded?

Spero Therapeutics was founded in 2013. It employs 11 to 50 people.

Where is Spero Therapeutics based?

Spero Therapeutics is headquartered in Cambridge, United States, in the North America region.

How does Spero Therapeutics make money?

Four revenue lines are on record. Licensing Royalties from GSK is the primary driver. The others are licensing Revenue from Pfizer, BARDA Grant Funding and revenue Interest Financing.

Who are Spero Therapeutics's main competitors?

Direct peers on record are Melinta Therapeutics, Tetraphase Biosciences, Paratek Pharmaceuticals, Iterum Therapeutics, Nabriva Therapeutics, Cidara Therapeutics and Innoviva Specialty Therapeutics (formerly Entasis/VenatoRx). Broad incumbents are GSK (GlaxoSmithKline) and Pfizer Inc.. BioMarin Pharmaceutical is listed as an emerging player.

Does Spero Therapeutics have an API?

No public API is recorded for Spero Therapeutics.

What industry is Spero Therapeutics in?

Spero Therapeutics's product category is Infectious Disease Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAG, Infectious Disease & Antimicrobials Pharmaceuticals, with a secondary code of HLAIACAF, Pulmonology & Allergy Specialty Pharmaceuticals. Its NAICS code is 541714 and its SIC code is 2834.

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Stock TitanSpero Therapeutics to Join Chardan Healthcare ConferenceSpero Therapeutics announced that CEO Esther Rajavelu will participate in a fireside chat at the Chardan 10th Annual Healthcare Conference on October 20, 2026, in New York City. The company's leadership team will also be available for one-on-one meetings, and a webcast replay will be available for about 90 days.GlobeNewswireComplicated Urinary Tract Infections Market Set for Expansion by 2036, Supported by Recent Drug Approvals Including GSK/Spero Therapeutics’ UTEBZI and Wockhardt’s ZAYNICH and Emerging Therapies | DelveInsightThe complicated urinary tract infections market is projected to grow through 2036, driven by antimicrobial resistance and rising cases. The US led the market in 2025, with 3.5 million incident cUTI cases in 2024. Emerging therapies like UTEBZI and ZAYNICH are expected to reshape the landscape.Markets DailyContrasting Jaguar Animal Health (NASDAQ:JAGX) & Spero Therapeutics (NASDAQ:SPRO)Spero Therapeutics outperforms Jaguar Animal Health on all 14 compared factors, including revenue, earnings, and analyst ratings. Spero has higher revenue ($66.80M vs $11.51M) and a positive net margin, while Jaguar is unprofitable. Analysts favor Spero with a consensus target price of $6.00.Ticker ReportHead to Head Review: Jaguar Animal Health (NASDAQ:JAGX) & Spero Therapeutics (NASDAQ:SPRO)Spero Therapeutics and Jaguar Animal Health are compared on 14 factors, with Spero winning on all. Spero has higher revenue and earnings, a stronger analyst consensus, and a higher upside target. Jaguar Animal Health is more affordable but less profitable.AInvestSPRO Explodes 18%: Micro-Cap Biotech Ignites with Relentless Volume SurgeSpero Therapeutics (SPRO) surged 17.98% intraday, closing near $1.345, with trading volume 17 times average. The micro-cap biotech's market cap expanded to $78.33 million on a liquidity-driven breakout, not a product or regulatory catalyst. Key resistance at $1.44 remains to be tested.Ticker ReportHead-To-Head Survey: ImmuCell (NASDAQ:ICCC) vs. Spero Therapeutics (NASDAQ:SPRO)Spero Therapeutics and ImmuCell are compared on revenue, earnings, valuation, and analyst ratings. Spero reports $66.80 million revenue and a 24.9% net margin, while ImmuCell reports $30.68 million revenue and a 2.57% net margin. Spero beats ImmuCell on 8 of 11 factors, including lower P/E and higher institutional ownership.AInvestInnovent announces 2026 interim results and business updatesInnovent Biologics reported first-half 2026 results with total revenue up 44.8% to RMB8.62 billion and product revenue up 56.7% to RMB8.20 billion, driven by its dual-engine strategy. Gross profit rose 43.0% to RMB7.32 billion, with IFRS net profit up 50.2% to RMB1.25 billion. The company will hold an interim results call on August 25, 2026, and recently signed an exclusive license with Spero Therapeutics for SP001.Ticker ReportCASI Pharmaceuticals (NASDAQ:CASI) and Spero Therapeutics (NASDAQ:SPRO) Financial SurveyA MarketBeat comparison evaluated CASI Pharmaceuticals and Spero Therapeutics across profitability, institutional ownership, valuation, earnings, analyst ratings and risk. Spero showed higher revenue ($66.80 million vs $26.85 million), net income ($8.57 million vs -$39.26 million) and margins, while CASI had a lower beta (0.91 vs 1.55) and a consensus price target of $4.00.PR NewswireInnovent Announces 2026 Interim Results and Business UpdatesInnovent Biologics reported H1 2026 revenue of RMB 8.6 billion, up 45% year-over-year, and net profit of RMB 1.3 billion. The company set 2030 targets of RMB 35-40 billion revenue and global Phase 3 launches. It also announced strategic collaborations with Takeda, Eli Lilly, and Pfizer.AInvestSpero Therapeutics: The Market Treated a Lifeline Like a Death Rattle (Accumulate)Spero Therapeutics secured FDA approval for its oral antibiotic Utebzi and raised $105 million through a non-recourse royalty financing deal with HealthCare Royalty, a fund under KKR. The company's pro-forma cash position of approximately $155 million significantly exceeds its current market capitalization of roughly $70 million, providing substantial liquidity despite the stock's recent decline. GSK is responsible for launching Utebzi in the US and Europe starting in 2026, while Spero retains 35% of royalty proceeds above debt obligations and continues development on its SP001 pipeline.