Company intelligence / Profile preview

UTILITY therapeutics

Altrincham, England, United Kingdomutilitytherapeutics.com ↗
Ownership
Private
Development stage
NDA
01

Overview

FDA approved PIVYA (pivmecillinam) for treatment of female adults with uncomplicated UTIs on April 25, 2024. Clinical trials showed 62% of 137 subjects achieved composite response compared to 10% with placebo. In another trial, 72% of 127 subjects achieved composite response compared to 76% with a comparator drug. In a third trial, 66% of 105 subjects achieved composite response compared to 22% with ibuprofen[5].

Therapeutic areas
Infectious Diseases
Modalities
Small moleculesAntibiotics
Industry
Biotech
02

Drug pipeline

2 assets

pivmecillinam

Approved

1 more asset in the full pipeline.

03

Partnerships

LEO Pharma A/S (license agreement for US rights to mecillinam and pivmecillinam)[6]

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