Last reviewed · How we verify

Myfortic plus low-dose steroid

The University of Hong Kong · FDA-approved active Small molecule

Myfortic (mycophenolate sodium) combined with low-dose corticosteroids suppresses T and B lymphocyte proliferation to prevent organ rejection, while the steroid provides additional anti-inflammatory effects.

Myfortic (mycophenolate sodium) combined with low-dose corticosteroids suppresses T and B lymphocyte proliferation to prevent organ rejection in transplant recipients. Used for Prevention of organ rejection in renal transplant recipients, Prevention of organ rejection in cardiac transplant recipients, Prevention of organ rejection in hepatic transplant recipients.

At a glance

Generic nameMyfortic plus low-dose steroid
Also known asMycophenolate sodium
SponsorThe University of Hong Kong
Drug classImmunosuppressant (inosine monophosphate dehydrogenase inhibitor)
TargetInosine monophosphate dehydrogenase (IMPDH), type II
ModalitySmall molecule
Therapeutic areaImmunology / Transplantation
PhaseFDA-approved

Mechanism of action

Mycophenolate sodium is a selective inhibitor of inosine monophosphate dehydrogenase (IMPDH), an enzyme critical for guanine nucleotide synthesis in lymphocytes. This preferentially depletes guanine nucleotides in T and B cells, inhibiting their proliferation. The addition of low-dose corticosteroids enhances immunosuppression through glucocorticoid receptor-mediated suppression of cytokine production and immune cell activation.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: