TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

MYHIBBIN

MYCOPHENOLATE MOFETIL
Immunology Approved 2024-05-01
1
Indication
--
Phase 3 Trials
1
Years on Market

Details

Status
Prescription
First Approved
2024-05-01
Routes
ORAL
Dosage Forms
SUSPENSION

Companies

Active Ingredient: MYCOPHENOLATE MOFETIL

MYHIBBIN Approval History

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What MYHIBBIN Treats

1 FDA approvals

Originally approved for its first indication in 2024 .

  • Other (1)

MYHIBBIN Boxed Warning

EMBRYOFETAL TOXICITY, MALIGNANCIES and SERIOUS INFECTIONS Use during pregnancy is associated with increased risks of first trimester pregnancy loss and congenital malformations. Avoid if safer treatment options are available. Females of reproductive potential must be counseled regarding pregnancy prevention and planning [see Warnings and Precautions (5.1) , Use in Special Populations (8.1 , 8.3) ] . Increased risk of development of lymphoma and other malignancies, particularly of the skin [see W...

MYHIBBIN Competitors

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9 other drugs also target MTOR. Compare mechanisms, indications, and trial activity.

View all 9 MTOR drugs →
Drug = Competitor name Company = Manufacturer N indic. = FDA-approved indications → Date = Patent/exclusivity expiry

Competitors share the same molecular target (MTOR). Earlier expiry dates signal biosimilar/generic opportunities.

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

MYHIBBIN FDA Label Details

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Indications & Usage

FDA Label (PDF)

MYHIBBIN is indicated for the prophylaxis of organ rejection, in adult and pediatric recipients 3 months of age and older of allogeneic kidney [see Clinical Studies ], heart [see Clinical Studies ] or liver transplants [see Clinical Studies ] , in combination with other immunosuppressants. MYHIBBIN is an antimetabolite immunosuppressant indicated for the prophylaxis of organ rejection in adult and pediatric recipients 3 months of age and older of allogeneic kidney, heart or liver transplants, in combination with other immunosuppressants.

⚠️ BOXED WARNING

WARNING: EMBRYOFETAL TOXICITY, MALIGNANCIES and SERIOUS INFECTIONS Use during pregnancy is associated with increased risks of first trimester pregnancy loss and congenital malformations. Avoid if safer treatment options are available. Females of reproductive potential must be counseled regarding pre...

MYHIBBIN Patents & Exclusivity

Latest Patent: Aug 2039

Patents (5 active)

US12194143 Expires Aug 16, 2039
US12097285 Expires Aug 16, 2039
US12226526 Expires Aug 16, 2039
US11931455 Expires Aug 16, 2039
US12097284 Expires Aug 16, 2039
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.