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LCP-tacrolimus QD + MMF QD then MMF QD

University Hospital, Limoges · FDA-approved active Small molecule

LCP-tacrolimus is a prolonged-release formulation of tacrolimus that suppresses T-cell activation and proliferation, combined with mycophenolate mofetil (MMF) which inhibits inosine monophosphate dehydrogenase to reduce lymphocyte proliferation, together providing dual immunosuppression.

LCP-tacrolimus is a prolonged-release formulation of tacrolimus that suppresses T-cell activation and proliferation, combined with mycophenolate mofetil (MMF) which inhibits inosine monophosphate dehydrogenase to reduce lymphocyte proliferation, together providing dual immunosuppression. Used for Organ transplant rejection prevention (renal, cardiac, hepatic transplantation).

At a glance

Generic nameLCP-tacrolimus QD + MMF QD then MMF QD
SponsorUniversity Hospital, Limoges
Drug classCalcineurin inhibitor + antimetabolite immunosuppressant combination
TargetCalcineurin (tacrolimus); inosine monophosphate dehydrogenase type II (MMF)
ModalitySmall molecule
Therapeutic areaImmunology / Transplantation
PhaseFDA-approved

Mechanism of action

Tacrolimus is a calcineurin inhibitor that blocks IL-2 production and T-cell activation by inhibiting the phosphatase calcineurin. MMF selectively inhibits type II inosine monophosphate dehydrogenase, preferentially affecting T and B lymphocyte proliferation. The combination provides synergistic immunosuppression for transplant rejection prevention, with LCP-tacrolimus offering once-daily dosing convenience compared to immediate-release formulations.

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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