Vijoice Patent Expiration

Vijoice is a drug owned by Novartis Pharmaceuticals Corp. It is protected by 4 US drug patents filed from 2022 to 2025 out of which none have expired yet. Vijoice's patents have been open to challenges since 25 May, 2023. Based on its patents and exclusivities, its generic launch date is estimated to be Feb 17, 2037. Details of Vijoice's patents and their expiration are given in the table below.

Patent strength
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Drug Patent Number Drug Patent Title Drug Patent Expiry Status
These drug patents protect the active ingredient(API) of the drug. Only drug patent owner can launch products that use this active ingredient until these patents expire.
US8227462 Pyrrolidine-1,2-dicarboxamide derivatives
Apr, 2033

(6 years from now)

Active
US8476268 Pyrrolidine-1,2-dicarboxamide derivatives
Sep, 2029

(2 years from now)

Active
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US12427141 Byl719 (Alpelisib) For Use In The Treatment Of Pik3Ca-Related Overgrowth Spectrum (Pros-Cloves Syndrome)
Feb, 2037

(10 years from now)

Active
US11433059 Byl719 (Alpelisib) For Use In The Treatment Of Pik3Ca-Related Overgrowth Spectrum (Pros-Cloves Syndrome)
Feb, 2037

(10 years from now)

Active


A patent's expiry date may change depending upon legal activities going on that patent. Critical activities like abandoning of a patent, term extension of a patent or amendment of its claims can increase or decrease the life of a patent hence affecting its expiry date and in turn affecting the generic launch date of that drug. Tracking these ongoing activities on a patent application helps to keep an eye on the latest developments in the patent process of the drug which can give an idea of how early a drug's generic could be available. The next section provides a list of recent legal activities on Vijoice's patents.

Given below is the list of recent legal activities going on the following patents of Vijoice.

Activity Date Patent Number
Patent litigations
Payment of Maintenance Fee, 4th Year, Large Entity 27 Feb, 2026 US11433059
Recordation of Patent Grant Mailed 07 Oct, 2025 US12427141
Patent eGrant Notification 30 Sep, 2025 US12427141
Patent Issue Date Used in PTA Calculation 30 Sep, 2025 US12427141
Recordation of Patent eGrant 30 Sep, 2025 US12427141
Mail Patent eGrant Notification 30 Sep, 2025 US12427141
Email Notification 30 Sep, 2025 US12427141
Email Notification 18 Sep, 2025 US12427141
Issue Notification Mailed 17 Sep, 2025 US12427141
Mail Response to 312 Amendment (PTO-271) 04 Sep, 2025 US12427141


FDA has granted several exclusivities to Vijoice. Till the time these exclusivities are active, no other company can market a generic or bioequivalent version of Vijoice, regardless of the status of it's patents. These exclusivities hence play a crucial role in delaying the generic launch. Given below are details of the exclusivities granted to Vijoice.

Exclusivity Information

Vijoice holds 2 exclusivities out of which 1 have expired. Its last outstanding exclusivity is set to expire in 2029. Details of Vijoice's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) May 24, 2024
Orphan Drug Exclusivity(ODE-396) Apr 05, 2029

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US patents provide insights into the exclusivity only within the United States, but Vijoice is protected by patents in multiple countries. Understanding the full scope of patent protection is crucial in strategizing market entry. By looking at the broader patent landscape, you can identify markets with weaker patent protection which could be ideal generic entry points. The following section offers details on Vijoice's family patents as well as insights into ongoing legal events on those patents.

Vijoice's Family Patents

Vijoice has patent protection in a total of 48 countries. It's US patent count contributes only to 8.8% of its total global patent coverage. 8 countries have all of their patents expired or invalidated which has opened up potential generic launch opportunities in these countries. Click below to unlock the full patent family tree for Vijoice.

Family Patents

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Clinical Trials

Recent Clinical Trials on Vijoice:

Sometimes companies keep conducting clinical trials even after the drug's approval to discover new formulations, methods of use, or new treatment indications, so they could file for additional patents or receive regulatory exclusivity extensions, such as pediatric exclusivity, potentially delaying generic competition. Based on these recent clinical trials, generic companies need to consider the potential for new intellectual property or regulatory hurdles. These strategic moves by the drug owner might delay generic substitution or lead to additional sales of the brand drug, even after patent expiry.

Title Lead Sponsor Collaborators Status Phases
Clinical Trials
Study of Alpelisib (BYL719) in Combination With Trastuzumab and Pertuzumab as Maintenance Therapy in Patients With HER2-positive Advanced Breast Cancer With a PIK3CA Mutation Novartis Pharmaceuticals NA ACTIVE NOT RECRUITING
(Sep 1, 2026)
PHASE3
Study Assessing the Efficacy and Safety of Treatment With Alpelisib Plus Fulvestrant in Japanese Men and Postmenopausal Women With Advanced Breast Cancer Novartis Pharmaceuticals NA ACTIVE NOT RECRUITING
(Sep 1, 2026)
PHASE2
Study Assessing the Efficacy and Safety of Treatment With Alpelisib Plus Fulvestrant Versus Placebo Plus Fulvestrant in Chinese Men and Postmenopausal Women With Advanced Breast Cancer Novartis Pharmaceuticals NA ACTIVE NOT RECRUITING
(Sep 1, 2026)
PHASE2
Study to Assess the Efficacy and Safety of Alpelisib Plus Fulvestrant in Participants With HR-positive (HR+), HER2-negative, Advanced Breast Cancer After Treatment With a CDK4/6 Inhibitor and an Aromatase Inhibitor. Novartis Pharmaceuticals NA ACTIVE NOT RECRUITING
(Sep 1, 2026)
PHASE3
Phase 1b Study of OP-1250 (Palazestrant) in Combination With Ribociclib, Alpelisib, Everolimus, or Atirmociclib in ER+, HER2- Breast Cancer Olema Pharmaceuticals, Inc. NA ACTIVE NOT RECRUITING
(Sep 1, 2026)
PHASE1
Targeted Therapy Directed by Genetic Testing in Treating Patients With Locally Advanced or Advanced Solid Tumors, The ComboMATCH Screening Trial National Cancer Institute (NCI) NA RECRUITING
(Sep 1, 2026)
PHASE2
Alpelisib in Pediatric and Adult Patients With Lymphatic Malformations Associated With a PIK3CA Mutation. Novartis Pharmaceuticals NA RECRUITING
(Sep 1, 2026)
PHASE2, PHASE3
EPIK-P4: A Phase II Single-arm Study to Assess the Efficacy, Safety and Pharmacokinetics of Alpelisib (BYL719) in Pediatric and Adult Patients With PIK3CA-related Overgrowth Spectrum (PROS) Novartis Pharmaceuticals NA RECRUITING
(Sep 1, 2026)
PHASE2
Roll-Over Study of Alpelisib (BYL719) for Continued Access and Long-Term Safety. Novartis Pharmaceuticals NA NOT YET RECRUITING
(Sep 1, 2026)
PHASE2
Alpelisib Challenge Test (ACT) Columbia University NA RECRUITING
(Sep 1, 2026)
PHASE1
Study Assessing the Efficacy and Safety of Alpelisib + Nab-paclitaxel in Subjects With Advanced TNBC Who Carry Either a PIK3CA Mutation or Have PTEN Loss Novartis Pharmaceuticals NA TERMINATED
(Aug 1, 2026)
PHASE3
Study Assessing the Efficacy, Safety and PK of Alpelisib (BYL719) in Pediatric and Adult Patients With PIK3CA-related Overgrowth Spectrum Novartis Pharmaceuticals NA ACTIVE NOT RECRUITING
(Aug 1, 2026)
PHASE2
Combination Trial of Tipifarnib and Alpelisib in Adult Recurrent/ Metastatic Head and Neck Squamous Cell Carcinoma (R/M HNSCC) Kura Oncology, Inc. NA COMPLETED
(Aug 1, 2026)
PHASE1, PHASE2
Preventing High Blood Sugar in People Being Treated for Metastatic Breast Cancer Memorial Sloan Kettering Cancer Center NA ACTIVE NOT RECRUITING
(Aug 1, 2026)
PHASE2
A Study Evaluating the Efficacy and Safety of Inavolisib Plus Fulvestrant Compared With Alpelisib Plus Fulvestrant in Participants With HR-Positive, HER2-Negative, PIK3CA Mutated, Locally Advanced or Metastatic Breast Cancer Post CDK4/6i and Endocrine Combination Therapy Hoffmann-La Roche NA RECRUITING
(Aug 1, 2026)
PHASE3
Human Models of Selective Insulin Resistance: Alpelisib, Part I Columbia University NA RECRUITING
(Aug 1, 2026)
PHASE1
Phase Ib Study of AlpeliSib With PEmbroLizumab in Patients With mEtastatic Breast caNcer or melanomA (SELENA) M.D. Anderson Cancer Center NA RECRUITING
(Aug 1, 2026)
PHASE1
A Study of Alpelisib and Fulvestrant to Treat Endometrial Cancer GOG Foundation NA ACTIVE NOT RECRUITING
(Jul 1, 2026)
PHASE2
Study of the Molecular Features of Postmenopausal Women With HR+ HER2-negative aBC on First-line Treatment With Ribociclib and Letrozole and, in Patients With a PIK3CA Mutation, on Second-line Treatment With Alpelisib Plus Fulvestrant Novartis Pharmaceuticals NA TERMINATED
(Jun 1, 2026)
PHASE3
Nab-paclitaxel and Alpelisib for the Treatment of Anthracycline Refractory Triple Negative Breast Cancer With PIK3CA or PTEN Alterations M.D. Anderson Cancer Center NA TERMINATED
(Jun 1, 2026)
PHASE2
Alpelisib Plus Olaparib in Platinum-resistant/Refractory, High-grade Serous Ovarian Cancer, With no Germline BRCA Mutation Detected Novartis Pharmaceuticals NA TERMINATED
(Jun 1, 2026)
PHASE3
Alpelisib/iNOS Inhibitor/Nab-paclitaxel in Patients With HER2 Negative Metaplastic Breast Cancer (MpBC) The Methodist Hospital Research Institute NA RECRUITING
(Jun 1, 2026)
PHASE2
SEQUence of Endocrine Therapy in Advanced Luminal Breast Cancer (SEQUEL-Breast) Borstkanker Onderzoek Groep NA ACTIVE NOT RECRUITING
(May 1, 2026)
PHASE2
Alpelisib And Sacituzumab Govitecan For Treatment Of Breast Cancer University of Kansas Medical Center NA ACTIVE NOT RECRUITING
(Apr 1, 2026)
PHASE1
Evexomostat Plus PI3K or AKT Inhibitor and Fulvestrant in Patients With a PI3K Alteration and HR+/Her2- Breast Cancer SynDevRx, Inc. NA RECRUITING
(Apr 1, 2026)
PHASE1, PHASE2
A Trial of Targeted Therapies for Patients With Slow-Flow or Fast-Flow Vascular Malformations Murdoch Childrens Research Institute NA RECRUITING
(Apr 1, 2026)
PHASE2
24VA022; VATCH Alpelisib for TIE2/PIK3CA Pathway VAs Children's Hospital of Philadelphia NA ACTIVE NOT RECRUITING
(Apr 1, 2026)
PHASE2
Clinical Trial of Alpelisb and Tucatinib in Patients With PIK3CA-Mutant HER2+ Metastatic Breast Cancer. Criterium, Inc. NA ACTIVE NOT RECRUITING
(Mar 1, 2026)
PHASE1, PHASE2
A Study to Evaluate the Efficacy and Safety of Everolimus in Patients With Teratment-refractory Vascular Anomalies Yonsei University NA NOT YET RECRUITING
(Mar 1, 2026)
PHASE2




Generic Launch

Generic Release Date:

Vijoice's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Feb 17, 2037 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Vijoice Generics:

There are no approved generic versions for Vijoice as of now.

Alternative Brands for Vijoice

There are several other brand drugs using the same active ingredient (Alpelisib) as Vijoice. Given below is the list of those companies and their brand drugs, to help you identify new opportunities, assess competitors, and plan your market strategies more effectively.

Drug Owner Drug Name
Novartis
Piqray






About Vijoice

Vijoice is a drug owned by Novartis Pharmaceuticals Corp. Vijoice uses Alpelisib as an active ingredient. Vijoice was launched by Novartis in 2022.

Approval Date:

Vijoice was approved by FDA for market use on 05 April, 2022.

NCE-1 date:

NCE-1 date also known as the four year date occurs four years after the original drug approval and marks the first opportunity for a generic manufacturer to file an ANDA with a Paragraph IV certification. This is the earliest point when generic competition might begin, provided the challenge is successful. Since the approval date for Vijoice is 05 April, 2022, its NCE-1 date is estimated to be 25 May, 2023.

Active Ingredient:

Vijoice uses Alpelisib as the active ingredient. Check out other Drugs and Companies using Alpelisib ingredient

Dosage:

Vijoice is available in the following dosage forms - granule form for oral use, tablet form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
125MG TABLET Prescription ORAL
200MG TABLET Prescription ORAL
50MG TABLET Prescription ORAL
50MG/PACKET GRANULE Prescription ORAL