Vyscoxa Patent Expiration

Vyscoxa is a drug owned by Carwin Pharmaceutical Associates Llc. It is protected by 1 US drug patent filed in 2026 out of which none have expired yet. Based on its patents and exclusivities, its generic launch date is estimated to be Sep 17, 2045. Details of Vyscoxa's patents and their expiration are given in the table below.

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Drug Patent Number Drug Patent Title Drug Patent Expiry Status
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US12678405 NA
Sep, 2045

(18 years from now)

Active

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US patents provide insights into the exclusivity only within the United States, but Vyscoxa 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 Vyscoxa's family patents as well as insights into ongoing legal events on those patents.

Vyscoxa's Family Patents


Family Patents

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Clinical Trials

Recent Clinical Trials on Vyscoxa:

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
Antiangiogenic Therapy for Children With Recurrent Medulloblastoma, Ependymoma, ATRT and Rare CNS Tumors Medical University of Vienna NA RECRUITING
(Sep 1, 2026)
PHASE2
Treating Immuno-metabolic Depression With Anti-inflammatory Drugs Amsterdam UMC, location VUmc NA COMPLETED
(Sep 1, 2026)
PHASE3
A Phase Ib Study to Evaluate the Efficacy and Safety of HRS-2129 in Patients With Knee Osteoarthritis Shandong Suncadia Medicine Co., Ltd. NA COMPLETED
(Sep 1, 2026)
PHASE1
Ivosidenib Plus mFOLFOXIRI and Celecoxib for BRAF-targeted Therapy-refractory BRAF V600E-mutant Colorectal Cancer Patients Sun Yat-sen University NA RECRUITING
(Sep 1, 2026)
PHASE2
A Trial in Healthy Participants to Assess Drug Interaction Potential of BGB-43395 BeOne Medicines NA NOT YET RECRUITING
(Sep 1, 2026)
PHASE1
PET Imaging of Cyclooxygenase in Participants With Major Depressive Disorder (MDD) National Institute of Mental Health (NIMH) NA RECRUITING
(Aug 14, 2026)
PHASE1
Rintatolimod, Celecoxib and Interferon Alpha 2b With Pembrolizumab For the Treatment of Patients With Metastatic or Unresectable Triple Negative Breast Cancer Roswell Park Cancer Institute NA TERMINATED
(Aug 1, 2026)
PHASE1, PHASE2
Intensive Locoregional Chemoimmunotherapy for Recurrent Ovarian Cancer Plus Intranodal DC Vaccines Roswell Park Cancer Institute NA WITHDRAWN
(Jul 1, 2026)
PHASE1, PHASE2
Evaluation of Superiority of Valsartan+Celecoxib+Metformin Over Metformin Alone in Type 2 Diabetes Patients ARKAY Therapeutics NA WITHDRAWN
(Jul 1, 2026)
PHASE1, PHASE2
Celecoxib for ENT Pain Management University of Wisconsin, Madison NA RECRUITING
(Jul 1, 2026)
PHASE2
TriGlytza®-01 Versus Metformin in Overweight and Obese Adults With Type 2 Diabetes and Inadequate Glycaemic Control Despite Metformin Therapy Myopharm Limited NA NOT YET RECRUITING
(Jul 1, 2026)
PHASE2
Celecoxib Plus R-CHOP vs R-CHOP in Newly Diagnosed Advanced CD5+ DLBCL Sun Yat-sen University NA RECRUITING
(Jul 1, 2026)
PHASE2
Celecoxib With Chemotherapy in Localized, Muscle-Invasive Bladder Cancer Baylor College of Medicine NA COMPLETED
(Jun 1, 2026)
PHASE1
Safety of F14 Following Total Knee Replacement Arthritis Innovation Corporation NA SUSPENDED
(Jun 1, 2026)
PHASE2, PHASE3
A Multicenter, Prospective, Randomized, Open-label Phase Ib/II Study of Celecoxib Plus Pembrolizumab and Gemcitabine/Cisplatin Versus Pembrolizumab and Gemcitabine/Cisplatin in Patients With CK5/6-High Unresectable Locally Advanced or Metastatic Intrahepatic Cholangiocarcinoma Shanghai 6th People's Hospital NA NOT YET RECRUITING
(Jun 1, 2026)
PHASE1, PHASE2
Intensive Locoregional Chemoimmunotherapy, Intradermal Autologous Alpha-DC1 Vaccines, and Systemic Pembrolizumab for Advanced-Stage Ovarian Cancer Kalinski, Pawel, MD, PhD NA NOT YET RECRUITING
(Jun 1, 2026)
PHASE2
Efficacy of Intravenous Dexamethasone in Prolonging the Duration of Spinal Anesthesia With Chloroprocaine in Knee Arthroscopy CMC Ambroise Paré NA NOT YET RECRUITING
(Jun 1, 2026)
PHASE3
Toripalimab Plus Celecoxib for dMMR/MSI-H Locally Advanced Colorectal Cancer Sun Yat-sen University NA RECRUITING
(May 1, 2026)
PHASE2
Methotrexate, Erlotinib, and Celecoxib for the Treatment of Recurrent/Metastatic Head and Neck Cancer in a Rural Midwest United States Population Mayo Clinic NA RECRUITING
(May 1, 2026)
PHASE2
Safety and Efficacy of Allogeneic Bone Marrow MSCs in Ankylosing Spondylitis Eighth Affiliated Hospital, Sun Yat-sen University NA NOT YET RECRUITING
(May 1, 2026)
PHASE1
Efficacy & Safety of rAd-IFN Administered With Celecoxib & Gemcitabine in Patients With Malignant Pleural Mesothelioma Ferring Ventures Limited NA COMPLETED
(Apr 1, 2026)
PHASE3
A Phase 2, Randomized, Prospective Double-Blind, Single-Center, Placebo-controlled Study to Evaluate Safety, Tolerability, Target Engagement, and Efficacy of PrimeC in Patients With Mild to Moderate Alzheimer's Disease. NeuroSense Therapeutics Ltd. NA TERMINATED
(Apr 1, 2026)
PHASE2
Efficacy and Safety of TRD205 Tablets for Postoperative Analgesia in Unilateral Total Hip Arthroplasty (Phase IIb) Beijing Tide Pharmaceutical Co., Ltd NA RECRUITING
(Apr 1, 2026)
PHASE2
Efficacy of Selective COX-2 Inhibitors in Relieving Orthodontic Pain Sharif Medical Research Center NA ACTIVE NOT RECRUITING
(Apr 1, 2026)
PHASE1
Metformin Safety and Efficacy in Osteoarthritis. Mostafa Bahaa NA RECRUITING
(Mar 1, 2026)
PHASE3
Study to Assess the Safety and Pharmacokinetics of AVD275 Injection in Patients With Osteoarthritis of the Knee Avidence Therapeutics NA RECRUITING
(Mar 1, 2026)
PHASE1




Generic Launch

Generic Release Date:

Vyscoxa's generic launch date based on the expiry of its last outstanding patent is estimated to be Sep 17, 2045 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Vyscoxa Generic API suppliers:

Celecoxib is the generic name for the brand Vyscoxa. 26 different companies have already filed for the generic of Vyscoxa, with Zydus Pharms having the maximum number of approved applications. Check out the entire list of companies who have already received approval for Vyscoxa's generic

Alternative Brands for Vyscoxa

There are several other brand drugs using the same active ingredient (Celecoxib) as Vyscoxa. 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
Kowa Pharms
Seglentis
Purple Biotech
Consensi
Scilex Pharms
Elyxyb
Upjohn
Celebrex


Apart from brand drugs containing the same ingredient, some generics have also been filed for Celecoxib, Vyscoxa's active ingredient. Check the complete list of approved generic manufacturers for Vyscoxa





About Vyscoxa

Vyscoxa is a drug owned by Carwin Pharmaceutical Associates Llc. Vyscoxa uses Celecoxib as an active ingredient. Vyscoxa was launched by Carwin Assoc in 2025.

Approval Date:

Vyscoxa was approved by FDA for market use on 29 July, 2025.

Active Ingredient:

Vyscoxa uses Celecoxib as the active ingredient. Check out other Drugs and Companies using Celecoxib ingredient

Dosage:

Vyscoxa is available in suspension form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
10MG/ML SUSPENSION Prescription ORAL