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Delamanid (DLM)

Wuhan Pulmonary Hospital · Phase 3 active Small molecule

Delamanid inhibits mycobacterial cell wall synthesis by targeting mycolic acid production, thereby killing Mycobacterium tuberculosis.

Delamanid inhibits mycobacterial cell wall synthesis by targeting mycolic acid production, thereby killing Mycobacterium tuberculosis. Used for Drug-resistant tuberculosis (MDR-TB and XDR-TB), Pulmonary tuberculosis in combination with other anti-TB agents.

At a glance

Generic nameDelamanid (DLM)
SponsorWuhan Pulmonary Hospital
Drug classMycobacterial cell wall synthesis inhibitor
TargetDprE1 (decaprenylphosphoryl-β-D-ribose 2'-epimerase)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Delamanid is a prodrug that is activated by mycobacterial enzymes to form reactive intermediates that inhibit the DprE1 enzyme, which is essential for the synthesis of mycolic acids—critical components of the mycobacterial cell wall. By disrupting cell wall integrity, delamanid leads to bacterial death and is particularly effective against drug-resistant tuberculosis strains.

Approved indications

Common side effects

Key clinical trials

Primary sources

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