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rifapentine + isoniazid

The Aurum Institute NPC · Phase 3 active Small molecule

Rifapentine inhibits the synthesis of mycolic acid in Mycobacterium tuberculosis, while isoniazid inhibits the synthesis of mycolic acid and the metabolism of fatty acids.

Rifapentine inhibits the synthesis of mycolic acid in Mycobacterium tuberculosis, while isoniazid inhibits the synthesis of mycolic acid and the metabolism of fatty acids. Used for Treatment of tuberculosis, Prevention of tuberculosis in HIV-infected individuals.

At a glance

Generic namerifapentine + isoniazid
Also known asPriftin (rifapentine)
SponsorThe Aurum Institute NPC
Drug classAntitubercular
ModalitySmall molecule
Therapeutic areaInfectious Diseases
PhasePhase 3

Mechanism of action

Rifapentine and isoniazid work synergistically to inhibit the growth of Mycobacterium tuberculosis by disrupting its cell wall synthesis and fatty acid metabolism. This leads to the death of the bacteria and ultimately, the resolution of tuberculosis infection.

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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