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PIP/TAZ FDC

Merck Sharp & Dohme LLC · Phase 3 active Small molecule

PIP/TAZ is a fixed-dose combination of piperacillin (a broad-spectrum beta-lactam antibiotic) and tazobactam (a beta-lactamase inhibitor) that works together to kill bacteria by inhibiting cell wall synthesis while protecting the antibiotic from enzymatic degradation.

PIP/TAZ is a fixed-dose combination of piperacillin (a broad-spectrum beta-lactam antibiotic) and tazobactam (a beta-lactamase inhibitor) that works together to kill bacteria by inhibiting cell wall synthesis while protecting the antibiotic from enzymatic degradation. Used for Bacterial infections (broad-spectrum coverage for intra-abdominal, gynecological, skin, and respiratory tract infections).

At a glance

Generic namePIP/TAZ FDC
SponsorMerck Sharp & Dohme LLC
Drug classBeta-lactam/beta-lactamase inhibitor combination
TargetBacterial penicillin-binding proteins; beta-lactamases
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Piperacillin is an extended-spectrum penicillin that binds to penicillin-binding proteins and disrupts bacterial cell wall synthesis. Tazobactam is a beta-lactamase inhibitor that irreversibly binds to and inactivates many beta-lactamases, preventing bacterial resistance mechanisms that would otherwise destroy piperacillin. Together, they provide enhanced coverage against beta-lactamase-producing gram-positive and gram-negative bacteria, as well as anaerobes.

Approved indications

Common side effects

Key clinical trials

Primary sources

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