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Mycophenolate mofetil, low dose steroid

Kyungpook National University Hospital · Phase 3 active Small molecule

Mycophenolate mofetil selectively inhibits inosine monophosphate dehydrogenase (IMPDH) in T and B lymphocytes, suppressing their proliferation, while low-dose corticosteroids provide additional anti-inflammatory and immunosuppressive effects.

Mycophenolate mofetil selectively inhibits inosine monophosphate dehydrogenase (IMPDH) in T and B lymphocytes, suppressing their proliferation, while low-dose corticosteroids provide additional anti-inflammatory and immunosuppressive effects. Used for Autoimmune diseases (likely lupus nephritis, vasculitis, or other systemic autoimmune conditions based on Phase 3 status).

At a glance

Generic nameMycophenolate mofetil, low dose steroid
Also known asMyconol, MMF
SponsorKyungpook National University Hospital
Drug classImmunosuppressant combination (inosine monophosphate dehydrogenase inhibitor + corticosteroid)
TargetIMPDH type II; glucocorticoid receptor
ModalitySmall molecule
Therapeutic areaImmunology
PhasePhase 3

Mechanism of action

Mycophenolate mofetil (MMF) is a prodrug that is converted to mycophenolic acid, which preferentially inhibits IMPDH type II, an enzyme critical for guanosine nucleotide synthesis in lymphocytes. This leads to selective depletion of T and B cell populations. The addition of low-dose corticosteroids enhances immunosuppression through glucocorticoid receptor-mediated inhibition of pro-inflammatory cytokine production and further lymphocyte suppression.

Approved indications

Common side effects

Key clinical trials

Primary sources

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