Generic Erivedge Availability
ERIVEDGE (vismodegib - capsule;oral)
Approval date: January 30, 2012
Strength(s): 150MG [RLD]
Has a generic version of Erivedge been approved?
No. There is currently no therapeutically equivalent version of Erivedge available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Erivedge. 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: About generic drugs.
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.
Pyridyl inhibitors of hedgehog signalling
Issued: February 15, 2011
Inventor(s): Gunzner; Janet L. & Sutherlin; Daniel & Stanley; Mark S. & Bao; Liang & Castanedo; Georgette M. & Lalonde; Rebecca L. & Wang; Shumei & Reynolds; Mark E. & Savage; Scott J. & Malesky; Kimberly & Dina; Michael S.
Assignee(s): Curis, Inc.
The invention provides novel inhibitors of hedgehog signaling that are useful as a therapeutic agents for treating malignancies where the compounds have the general formula I: wherein A, X, Y R1, R2, R3, R4, m and n are as described herein.Patent expiration dates:
- November 11, 2028✓✓
- November 11, 2028
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:
- January 30, 2017 -
- Erivedge Consumer Information (Drugs.com)
- Erivedge Consumer Information (Wolters Kluwer)
- Erivedge Consumer Information (Cerner Multum)
- Erivedge Advanced Consumer Information (Micromedex®)
- Erivedge AHFS DI Monographs (ASHP)
- Vismodegib Consumer Information (Wolters Kluwer)
- Vismodegib Consumer Information (Cerner Multum)
- Vismodegib Advanced Consumer Information (Micromedex®)
- Vismodegib AHFS DI Monographs (ASHP)
|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.|