Overview
Mycophenolate mofetil, also known as MMF or CellCept, is a prodrug of mycophenolic acid, and classified as a reversible inhibitor of inosine monophosphate dehydrogenase (IMPDH). This drug is an immunosuppressant combined with drugs such as Cyclosporine and corticosteroids to prevent organ rejection after hepatic, renal, and cardiac transplants. It is marketed by Roche Pharmaceuticals and was granted FDA approval for the prophylaxis of transplant rejection in 1995. In addition to the above uses, mycophenolate mofetil has also been studied for the treatment of nephritis and other complications of autoimmune diseases. Unlike another immunosuppressant class, the calcineurin inhibitors, MMF generally does not cause nephrotoxicity or fibrosis. Previously, mycophenolic acid (MPA) was administered to individuals with autoimmune diseases beginning in the 1970s, but was discontinued due to gastrointestinal effects and concerns over carcinogenicity. The new semi-synthetic 2-morpholinoethyl ester of MPA was synthesized to avoid the gastrointestinal effects associated with the administration of MPA. It demonstrates an increased bioavailability, a higher efficacy, and reduced gastrointestinal effects when compared to MPA.
Indication
Mycophenolate mofetil is indicated in combination with other immunosuppressants to prevent the rejection of kidney, heart, or liver transplants in adult and pediatric patients ≥3 months old. Mycophenolate mofetil may also be used off-label as a second-line treatment for autoimmune hepatitis that has not responded adequately to first-line therapy. Other off-label uses of this drug include lupus-associated nephritis and dermatitis in children.
Associated Conditions
- Transplanted Organ Rejection
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/05/30 | Phase 1 | Not yet recruiting | City of Hope Medical Center | ||
2025/05/15 | Phase 2 | Not yet recruiting | |||
2025/03/12 | Phase 2 | Recruiting | |||
2025/02/04 | Phase 2 | Recruiting | |||
2025/01/23 | Not Applicable | Not yet recruiting | |||
2024/12/31 | Phase 2 | Recruiting | |||
2024/11/12 | Phase 3 | Recruiting | |||
2024/11/08 | Phase 2 | Recruiting | Leland Metheny | ||
2024/10/29 | Not Applicable | Recruiting | Wen Zhang | ||
2024/05/14 | Phase 2 | Recruiting |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Camber Pharmaceuticals, Inc. | 31722-878 | ORAL | 250 mg in 1 1 | 8/2/2025 | |
Akorn | 17478-957 | INTRAVENOUS | 500 mg in 20 mL | 1/25/2024 | |
Amneal Pharmaceuticals LLC | 70121-1584 | INTRAVENOUS | 500 mg in 20 mL | 5/18/2023 | |
Aphena Pharma Solutions - Tennessee, LLC | 71610-033 | ORAL | 500 mg in 1 1 | 2/20/2024 | |
Teva Pharmaceuticals USA, Inc. | 0480-3571 | ORAL | 500 mg in 1 1 | 1/17/2022 | |
Steriscience Pte. Limited | 81293-000 | INTRAVENOUS | 500 mg in 20 mL | 4/11/2023 | |
Meitheal Pharmaceuticals Inc. | 71288-803 | INTRAVENOUS | 500 mg in 20 mL | 11/8/2023 | |
Amneal Pharmaceuticals NY LLC | 69238-1595 | ORAL | 200 mg in 1 mL | 12/30/2022 | |
Genentech, Inc. | 0004-0260 | ORAL | 500 mg in 1 1 | 2/21/2024 | |
Sandoz Inc | 0781-2067 | ORAL | 250 mg in 1 1 | 6/20/2022 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
Authorised | 2/21/2008 | ||
Authorised | 2/14/1996 | ||
Authorised | 10/7/2010 | ||
Authorised | 2/21/2008 |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
MOFECON 500 FILM-COATED TABLETS 500 MG | SIN16010P | TABLET, FILM COATED | 500 mg | 9/18/2020 | |
CELLCEPT TABLET 500 mg | SIN10032P | TABLET, FILM COATED | 500 mg | 9/24/1998 | |
MYFENAX FILM-COATED TABLETS 500MG | SIN13986P | TABLET, FILM COATED | 500mg | 7/14/2011 | |
TRANSTERO MYCOPHENOLATE MOFETIL CAPSULES 250MG USP | SIN16175P | CAPSULE | 250.000 mg | 4/30/2021 | |
REFRAT TABLET 500mg | SIN13695P | TABLET, FILM COATED | 500 mg | 8/20/2009 | |
MOFECON 250 CAPSULES 250 MG | SIN16011P | CAPSULE | 250 mg | 9/18/2020 | |
MYCOPHENOLATE MOFETIL CAPSULES 250MG | SIN14674P | CAPSULE | 250mg | 11/20/2014 | |
CELLCEPT CAPSULE 250 mg | SIN09279P | CAPSULE | 250 mg | 3/26/1997 | |
MYCOFIT 250 CAPSULE 250 MG | SIN15596P | CAPSULE, GELATIN COATED | 250 mg | 12/14/2018 | |
CELLCEPT FOR I.V. INFUSION 500 mg/vial | SIN11328P | INJECTION, POWDER, FOR SOLUTION | 500 mg/vial | 5/22/2000 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
CELLCEPT TAB 500MG | N/A | N/A | N/A | 2/19/1999 | |
MYCOPHENOLATE MOFETIL CAPSULES USP 250MG | N/A | N/A | N/A | 2/23/2017 | |
CELLCEPT POWDER FOR ORAL SUSPENSION 1G/5ML | N/A | N/A | N/A | 1/2/2014 | |
CELLCEPT TABLETS 500MG | N/A | N/A | N/A | 1/3/2018 | |
CELLCEPT CAP 250MG | N/A | N/A | N/A | 2/12/1997 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
MYCOPHENOLATE GH mycophenolate mofetil 500 mg tablet blister pack | 318884 | Medicine | A | 10/8/2019 | |
APO-MYCOPHENOLATE mycophenolate mofetil 250 mg capsule bottle | 168108 | Medicine | A | 11/8/2011 | |
APOTEX-MYCOPHENOLATE mycophenolate mofetil 250 mg capsule blister pack | 168106 | Medicine | A | 11/8/2011 | |
MYCOKEM 500 mycophenolate mofetil 500mg tablet blister pack | 262301 | Medicine | A | 12/16/2015 | |
ARX-Mycophenolate mycophenolate mofetil 500mg tablet blister pack | 235572 | Medicine | A | 11/17/2015 | |
CELLCEPT mycophenolate mofetil 250mg capsule | 67313 | Medicine | A | 11/2/1999 | |
PC-MYCOPHENOLATE 500 mycophenolate mofetil 500mg tablet blister pack | 262302 | Medicine | A | 12/16/2015 | |
MOFIT 500 mycophenolate mofetil 500 mg film coated tablet blister | 363771 | Medicine | A | 4/22/2022 | |
MYCOPHENOLATE SANDOZ mycophenolate mofetil 500mg tablet blister pack | 148225 | Medicine | A | 12/8/2008 | |
CELLCEPT mycophenolate mofetil 200mg/mL suspension bottle | 72582 | Medicine | A | 3/14/2000 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
CELLCEPT | Hoffmann-La Roche Limited | 02242145 | Powder For Suspension - Oral | 200 MG / ML | 8/27/2002 |
AG-MYCOPHENOLATE | angita pharma inc. | 02497182 | Tablet - Oral | 500 MG | N/A |
MYLAN-MYCOPHENOLATE | Mylan Pharmaceuticals ULC | 02371154 | Capsule - Oral | 250 MG | 11/30/2011 |
ACCEL-MYCOPHENOLATE MOFETIL TABLETS | accel pharma inc | 02400723 | Tablet - Oral | 500 MG | N/A |
APO-MYCOPHENOLATE MOFETIL | 02513722 | Tablet - Oral | 500 MG | N/A | |
TEVA-MYCOPHENOLATE | teva canada limited | 02364883 | Capsule - Oral | 250 MG | 11/30/2011 |
TARO-MYCOPHENOLATE | sun pharma canada inc | 02389754 | Tablet - Oral | 500 MG | N/A |
JAMP-MYCOPHENOLATE | 02380382 | Tablet - Oral | 500 MG | 3/23/2012 | |
ACH-MYCOPHENOLATE | 02378574 | Tablet - Oral | 500 MG | 2/16/2012 | |
MYLAN-MYCOPHENOLATE | Mylan Pharmaceuticals ULC | 02370549 | Tablet - Oral | 500 MG | 11/30/2011 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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