Company intelligence / Profile preview

Spero Therapeutics

Cambridge, Massachusetts, United Statessperotherapeutics.com ↗
Ownership
Public · SPRO
Employees
~75
Development stage
Phase 3
01

Overview

Spero’s lead asset, tebipenem HBr, an oral carbapenem antibiotic for cUTI and AP, is in a global Phase 3 trial (“PIVOT-PO”) with enrollment expected to complete in the second half of 2025. If approved, it would be the first oral carbapenem for these indications. SPR720 completed enrollment in a Phase 2a proof-of-concept trial for NTM-PD; topline data are expected Q4 2024 but development has been suspended pending full data review due to disappointing results and safety concerns. The SPR206 program was discontinued after pipeline reprioritization in early 2025.

Therapeutic areas
Infectious Diseases
Modalities
Small molecules (oral antibiotics)
Industry
Biotech
02

Drug pipeline

6 assets

tebipenem

3

5 more assets in the full pipeline.

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03

Partnerships

GlaxoSmithKline (GSK) – exclusive license agreement to commercialize tebipenem HBr outside certain Asian territories; GSK provided $66 million upfront and milestone payments supporting ongoing developmentU.S. government agencies previously supported now-discontinued programs via funding from Department of Defense, NIH/NIAID/HHS
04

Financials

Market cap
$68.9M
Total revenue
$0
Enterprise value
$20.2M

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