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Mycophenolate to sirolimus switch

London Health Sciences Centre · FDA-approved active Small molecule

Mycophenolate to sirolimus switch is a Immunosuppressant combination therapy Small molecule drug developed by London Health Sciences Centre. It is currently FDA-approved for Organ transplant recipients (kidney, heart, liver) requiring immunosuppressive therapy optimization. Also known as: rapamune, rapamycin, mycophenolic mofetil, mycophenolic acid.

A therapeutic strategy that replaces mycophenolate mofetil with sirolimus to reduce immunosuppressive burden while maintaining graft protection in transplant recipients.

A therapeutic strategy that switches patients from mycophenolate mofetil (an inosine monophosphate dehydrogenase inhibitor) to sirolimus (an mTOR inhibitor) to optimize immunosuppression in transplant recipients. Used for Organ transplant rejection prevention (switch strategy in transplant recipients).

At a glance

Generic nameMycophenolate to sirolimus switch
Also known asrapamune, rapamycin, mycophenolic mofetil, mycophenolic acid, cellcept
SponsorLondon Health Sciences Centre
Drug classImmunosuppressant combination therapy
TargetmTOR (sirolimus component); IMPDH (mycophenolate component being replaced)
ModalitySmall molecule
Therapeutic areaImmunology / Transplantation
PhaseFDA-approved

Mechanism of action

This represents a clinical protocol switch from mycophenolate (an inosine monophosphate dehydrogenase inhibitor that suppresses T and B cell proliferation) to sirolimus (an mTOR inhibitor with anti-proliferative and immunomodulatory effects). The switch aims to optimize long-term immunosuppressive therapy by leveraging sirolimus's distinct mechanism and potentially improved safety profile in certain transplant populations.

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 Mycophenolate to sirolimus switch

What is Mycophenolate to sirolimus switch?

Mycophenolate to sirolimus switch is a Immunosuppressant combination therapy drug developed by London Health Sciences Centre, indicated for Organ transplant recipients (kidney, heart, liver) requiring immunosuppressive therapy optimization.

How does Mycophenolate to sirolimus switch work?

A therapeutic strategy that replaces mycophenolate mofetil with sirolimus to reduce immunosuppressive burden while maintaining graft protection in transplant recipients.

What is Mycophenolate to sirolimus switch used for?

Mycophenolate to sirolimus switch is indicated for Organ transplant recipients (kidney, heart, liver) requiring immunosuppressive therapy optimization.

Who makes Mycophenolate to sirolimus switch?

Mycophenolate to sirolimus switch is developed and marketed by London Health Sciences Centre (see full London Health Sciences Centre pipeline at /company/london-health-sciences-centre).

Is Mycophenolate to sirolimus switch also known as anything else?

Mycophenolate to sirolimus switch is also known as rapamune, rapamycin, mycophenolic mofetil, mycophenolic acid, cellcept.

What drug class is Mycophenolate to sirolimus switch in?

Mycophenolate to sirolimus switch belongs to the Immunosuppressant combination therapy class. See all Immunosuppressant combination therapy drugs at /class/immunosuppressant-combination-therapy.

What development phase is Mycophenolate to sirolimus switch in?

Mycophenolate to sirolimus switch is FDA-approved (marketed).

What are the side effects of Mycophenolate to sirolimus switch?

Common side effects of Mycophenolate to sirolimus switch include Hyperlipidemia, Thrombocytopenia, Delayed wound healing, Mouth ulcers, Pneumonitis.

What does Mycophenolate to sirolimus switch target?

Mycophenolate to sirolimus switch targets mTOR (sirolimus component); IMPDH (mycophenolate component being replaced) and is a Immunosuppressant combination therapy.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing