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Spero Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 3·Cambridge, MA, United States·CEO: Ms. Esther P. Rajavelu
OncologyInfectious DiseaseMetabolicRespiratory

SPRO evidence brief

What we can confirm

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What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

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BioSniper AIPage evidence connected

Prepared research question

What matters most for SPRO—catalysts, financial risk and supporting evidence?

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Traceable citations · Unknowns marked

BioSniper AI · SPRO

Spero Therapeutics, Inc. is a biopharmaceutical company focused on developing and commercializing novel treatments for bacterial infections, with its lead product candidate tebipenem HBr targeting complicated urinary tract infections. As of June 30, 2026, the company reported cash and equivalents of $50.8 million and a net loss of $9.6 million for the quarter.

Key risk: Regulatory approval uncertainty

7.3/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$69.9M

Cash Runway

28.6 mo

Lead Asset

spr206 (Phase 2)

Next Catalyst

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 3 clinical trials for Spero Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

Spero Therapeutics, Inc. is a biopharmaceutical company focused on developing and commercializing novel treatments for bacterial infections, with its lead product candidate tebipenem HBr targeting complicated urinary tract infections. As of June 30, 2026, the company reported cash and equivalents of $50.8 million and a net loss of $9.6 million for the quarter.

  • Spero Therapeutics is developing tebipenem HBr, an oral carbapenem antibiotic for complicated urinary tract infections (cUTI) [sec_mda · as of 2026-08-12].
  • As of June 30, 2026, the company had cash and cash equivalents of $50.8 million [sec_mda · as of 2026-08-12].
  • The company reported a net loss of $9.6 million for the quarter ended June 30, 2026 [sec].
  • Spero has completed the PIVOT-PO Phase 3 trial for tebipenem HBr and ceased related clinical expenses [sec_mda · as of 2025-11-13].
  • The company has a royalty financing transaction that closed in 2026, providing additional funding [sec_mda · as of 2026-08-12].

What works

  • Spero has a late-stage asset, tebipenem HBr, which completed a Phase 3 trial (PIVOT-PO) for cUTI, reducing clinical development risk [sec_mda · as of 2025-11-13].
  • The company secured a royalty financing transaction in 2026, providing non-dilutive capital to extend its cash runway [sec_mda · as of 2026-08-12].
  • Spero has a partnership with GSK, including earned and non-contingent development milestone payments, which provided $23.8 million in funding [sec_mda · as of 2025-08-12].

What to weigh

  • Spero has no approved products and has not generated any revenue from product sales, as reflected in total revenue of $0.0 million for the quarter ended June 30, 2026 [sec].
  • The company has a history of operating losses, with a net loss of $9.6 million for the quarter ended June 30, 2026 [sec].
  • Spero's ability to continue as a going concern is dependent on its cash position and future financing, as the company evaluates conditions that raise substantial doubt about its viability [sec_mda · as of 2026-08-12].
  • The company faces regulatory uncertainty regarding FDA approval of tebipenem HBr, including potential requirements for additional clinical data [sec · filed 2024-10-29].

From the filings

Quoted directly from source documents.

  • Cash position as of June 30, 2026

    As of June 30, 2026, we had cash and cash equivalents of $50.8 million.

    SEC MD&A · August 12, 2026

  • Completion of PIVOT-PO Phase 3 trial

    the decrease in clinical expense as a result of the completion of the PIVOT-PO Phase 3 trial for tebipenem HBr and the decision to cease

    SEC MD&A · November 13, 2025

  • Royalty financing transaction closed in 2026

    together with proceeds from the royalty financing transaction that closed in J

    SEC MD&A · August 12, 2026

Risks & what to watch (4)

Key risks

  • Regulatory approval uncertaintyFDA may require additional clinical data or delay approval of tebipenem HBr [sec · filed 2024-10-29].
  • Going concern riskCompany must evaluate conditions that raise substantial doubt about its ability to continue as a going concern [sec_mda · as of 2026-08-12].
  • No product revenueSpero has no approved products and reported $0.0 million in total revenue for Q2 2026 [sec].
  • Dependence on single assetCompany's pipeline is heavily reliant on tebipenem HBr for cUTI [sec_mda · as of 2026-08-12].

What to watch

  • FDA decision on tebipenem HBr for complicated urinary tract infections [sec · filed 2024-10-29].
  • Cash runway and potential need for additional financing given net losses [sec_mda · as of 2026-08-12].
  • Progress of any partnership or licensing deals to expand pipeline [sec_mda · as of 2026-08-12].

Sources: SEC filings · SEC MD&A · Generated August 29, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway7.9

28.6 months

Financial Health9.7

D/E 0.19 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth5.9

3 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal4.3

0 buys · 1 sell (180d)

Runway

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

46

Total value held

$22.2M

Showing top 10 of 46 institutional holders of Spero Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 20, 2026
% of float
1.3%
Days to cover
1.9
Shares short
605,311
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

SPRO short interest

Governance

Frequently asked questions

What is the AI investment thesis for Spero Therapeutics, Inc.?

Spero Therapeutics, Inc. is a biopharmaceutical company focused on developing and commercializing novel treatments for bacterial infections, with its lead product candidate tebipenem HBr targeting complicated urinary tract infections. As of June 30, 2026, the company reported cash and equivalents of $50.8 million and a net loss of $9.6 million for the quarter.

What is Spero Therapeutics, Inc.'s lead drug candidate?

Spero Therapeutics, Inc.'s most advanced tracked candidate is spr206 (Phase 2) for MDR Gram-negative bacterial infections.

Who is the CEO of Spero Therapeutics, Inc.?

Ms. Esther P. Rajavelu is the chief executive officer of Spero Therapeutics, Inc. (SPRO).

Where is Spero Therapeutics, Inc. headquartered?

Spero Therapeutics, Inc. (SPRO) is headquartered in Cambridge, MA, United States.

What therapeutic areas does Spero Therapeutics, Inc. focus on?

Spero Therapeutics, Inc. develops therapies across Oncology, Infectious Disease, Metabolic, Respiratory.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.