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Intravenous iclaprim

Arpida AG · Phase 3 active Small molecule

Iclaprim is a dihydrofolate reductase (DHFR) inhibitor that disrupts bacterial folate metabolism, preventing DNA synthesis and bacterial growth.

Iclaprim is a dihydrofolate reductase (DHFR) inhibitor that disrupts bacterial folate metabolism, preventing DNA synthesis and bacterial growth. Used for Complicated skin and soft tissue infections (cSSTI), Hospital-acquired bacterial pneumonia (HABP) / Ventilator-associated bacterial pneumonia (VABP).

At a glance

Generic nameIntravenous iclaprim
SponsorArpida AG
Drug classDihydrofolate reductase inhibitor
TargetDihydrofolate reductase (DHFR)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Iclaprim binds to bacterial dihydrofolate reductase with high affinity, blocking the conversion of dihydrofolate to tetrahydrofolate, which is essential for one-carbon transfer reactions and nucleotide synthesis. This mechanism is bacteriostatic and selective for bacterial DHFR over human DHFR, making it suitable for treating bacterial infections. The drug has activity against a broad spectrum of gram-positive and some gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA).

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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