MedPath

FN-1501

Generic Name
FN-1501
Brand Names
Cellcept, Myfenax, CellCept, Mycophenolate mofetil Teva, Myclausen
Drug Type
Small Molecule
Chemical Formula
C22H25N9O
CAS Number
1429515-59-2
Unique Ingredient Identifier
6MC966B505

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

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

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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