Generic Joenja Availability
Last updated on Sep 11, 2024.
Joenja is a brand name of leniolisib, approved by the FDA in the following formulation(s):
JOENJA (leniolisib phosphate - tablet;oral)
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Manufacturer: PHARMING
Approval date: March 24, 2023
Strength(s): EQ 70MG BASE [RLD]
Has a generic version of Joenja been approved?
No. There is currently no therapeutically equivalent version of Joenja available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Joenja. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: Generic Drug FAQ.
Related patents
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
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Tetrahydro-pyrido-pyrimidine derivatives
Patent 8,653,092
Issued: February 18, 2014
Inventor(s): Cooke Nigel Graham & Fernandes Gomes Dos Santos Paulo & Graveleau Nadege & Hebach Christina & Högenauer Klemens & Hollingworth Gregory & Smith Alexander Baxter & Soldermann Nicolas & Stowasser Frank & Strang Ross & Tufilli Nicola & Von Matt Anette & Wolf Romain & Zecri Frédéric
Assignee(s): Novartis AGThe invention relates to substituted tetrahydro-pyrido-pyrimidine derivatives of the formula (I),
Patent expiration dates:
- February 19, 2032✓✓
- February 19, 2032
Related exclusivities
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
Exclusivity expiration dates:
- March 24, 2028 - NEW CHEMICAL ENTITY
- March 24, 2030 - TREATMENT OF ACTIVATED PHOSPHOINOSITIDE 3-KINASE DELTA (PI3K DELTA) SYNDROME (APDS) IN ADULT AND PEDIATRIC PATIENTS 12 YEARS OF AGE AND OLDER
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Glossary
| Term | Definition |
|---|---|
| Drug Patent | A drug patent is assigned by the U.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can be variable based on many factors, including development of new formulations of the original chemical, and patent infringement litigation. |
| Drug Exclusivity | Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant. |
| RLD | A Reference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (ANDA). By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
