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Mycophénolate Mofétil

University Hospital, Limoges · FDA-approved active Small molecule

Mycophénolate Mofétil is a Inosine monophosphate dehydrogenase (IMPDH) inhibitor Small molecule drug developed by University Hospital, Limoges. It is currently FDA-approved for Prevention of organ transplant rejection (renal, cardiac, hepatic), Active lupus nephritis, Autoimmune conditions requiring immunosuppression.

Mycophenolate mofetil inhibits inosine monophosphate dehydrogenase (IMPDH), selectively suppressing T and B lymphocyte proliferation to prevent immune rejection.

Mycophenolate mofetil inhibits inosine monophosphate dehydrogenase (IMPDH), selectively suppressing T and B lymphocyte proliferation to prevent immune rejection. Used for Prevention of acute organ rejection in patients receiving allogeneic renal, cardiac, or hepatic transplants, Treatment of active lupus nephritis, Treatment of autoimmune conditions including rheumatoid arthritis and other systemic autoimmune diseases.

At a glance

Generic nameMycophénolate Mofétil
SponsorUniversity Hospital, Limoges
Drug classInosine monophosphate dehydrogenase (IMPDH) inhibitor
TargetIMPDH type II
ModalitySmall molecule
Therapeutic areaImmunology
PhaseFDA-approved

Mechanism of action

MMF is a prodrug that is rapidly hydrolyzed to mycophenolic acid (MPA), which preferentially inhibits IMPDH type II, the predominant isoform in activated lymphocytes. This blocks guanosine nucleotide synthesis required for lymphocyte DNA replication, thereby reducing T and B cell proliferation without affecting other cell types as severely. It is used as an immunosuppressant to prevent organ transplant rejection and treat autoimmune conditions.

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

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Frequently asked questions about Mycophénolate Mofétil

What is Mycophénolate Mofétil?

Mycophénolate Mofétil is a Inosine monophosphate dehydrogenase (IMPDH) inhibitor drug developed by University Hospital, Limoges, indicated for Prevention of organ transplant rejection (renal, cardiac, hepatic), Active lupus nephritis, Autoimmune conditions requiring immunosuppression.

How does Mycophénolate Mofétil work?

Mycophenolate mofetil inhibits inosine monophosphate dehydrogenase (IMPDH), selectively suppressing T and B lymphocyte proliferation to prevent immune rejection.

What is Mycophénolate Mofétil used for?

Mycophénolate Mofétil is indicated for Prevention of organ transplant rejection (renal, cardiac, hepatic), Active lupus nephritis, Autoimmune conditions requiring immunosuppression.

Who makes Mycophénolate Mofétil?

Mycophénolate Mofétil is developed and marketed by University Hospital, Limoges (see full University Hospital, Limoges pipeline at /company/university-hospital-limoges).

What drug class is Mycophénolate Mofétil in?

Mycophénolate Mofétil belongs to the Inosine monophosphate dehydrogenase (IMPDH) inhibitor class. See all Inosine monophosphate dehydrogenase (IMPDH) inhibitor drugs at /class/inosine-monophosphate-dehydrogenase-impdh-inhibitor.

What development phase is Mycophénolate Mofétil in?

Mycophénolate Mofétil is FDA-approved (marketed).

What are the side effects of Mycophénolate Mofétil?

Common side effects of Mycophénolate Mofétil include Gastrointestinal disturbances (diarrhea, nausea, vomiting, abdominal pain), Leukopenia, Anemia, Infection, Headache, Tremor.

What does Mycophénolate Mofétil target?

Mycophénolate Mofétil targets IMPDH type II and is a Inosine monophosphate dehydrogenase (IMPDH) inhibitor.

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