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RIFAMPIN

FDA-approved approved Small molecule Verified Quality 80/100

Rifampin inhibits DNA-dependent RNA polymerase activity in susceptible Mycobacterium tuberculosis organisms.

Rifampin is a small molecule antibiotic used primarily for treating tuberculosis and eliminating meningococcal carriage. It inhibits bacterial RNA polymerase, preventing RNA synthesis. Approved by the FDA, it is part of multi-drug regimens for TB, offering a robust mechanism against Mycobacterium tuberculosis. Rifampin's unique mechanism and broad spectrum of activity differentiate it from other antibiotics. Despite its efficacy, it has significant drug interactions and potential hepatotoxicity, limiting its use in certain patient populations. Commercially, rifampin is a generic drug with widespread use in global TB control programs.

At a glance

Generic nameRIFAMPIN
Also known asrifampicin
Drug classRifamycin Antibacterial [EPC]
TargetDNA-dependent RNA polymerase
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved
First approval1971

Mechanism of action

Rifampin works by binding to the β-subunit of bacterial RNA polymerase, preventing the enzyme from synthesizing RNA. This inhibition stops the bacteria from producing essential proteins, leading to cell death. Rifampin is highly selective for bacterial RNA polymerase and does not affect the mammalian enzyme, making it safe for human use.

Approved indications

Pipeline indications

Common side effects

Drug interactions

Key clinical trials

Patents

PatentExpiryType

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

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