Gemtesa Patent Expiration

Gemtesa is a drug owned by Urovant Sciences Gmbh. It is protected by 3 US drug patents filed from 2021 to 2024 out of which none have expired yet. Gemtesa's patents have been open to challenges since 23 December, 2024. Based on its patents and exclusivities, its generic launch date is estimated to be Mar 22, 2040. Details of Gemtesa's patents and their expiration are given in the table below.

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.
US8247415 Hydroxymethyl pyrrolidines as β3 adrenergic receptor agonists
Dec, 2030

(5 years from now)

Active
US8653260 Hydroxymethyl pyrrolidines as beta 3 adrenergic receptor agonists
Apr, 2029

(4 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).
US12102638 Use of vibegron to treat overactive bladder
Mar, 2040

(15 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 Gemtesa's patents.

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

Activity Date Patent Number
Patent litigations
transaction for FDA Determination of Regulatory Review Period 29 Feb, 2024 US8247415
transaction for FDA Determination of Regulatory Review Period 29 Feb, 2024 US8653260
Payment of Maintenance Fee, 12th Year, Large Entity 05 Feb, 2024 US8247415
Second letter to regulating agency to determine regulatory review period 06 Feb, 2023 US8247415
Second letter to regulating agency to determine regulatory review period 06 Feb, 2023 US8653260
Letter from FDA or Dept of Agriculture re PTE application 18 Jan, 2023 US8247415
Letter from FDA or Dept of Agriculture re PTE application 18 Jan, 2023 US8653260
Initial letter Re: PTE Application to regulating agency 30 Nov, 2021 US8247415
Initial letter Re: PTE Application to regulating agency 30 Nov, 2021 US8653260
Payment of Maintenance Fee, 8th Year, Large Entity 30 Jul, 2021 US8653260


FDA has granted several exclusivities to Gemtesa. Till the time these exclusivities are active, no other company can market a generic or bioequivalent version of Gemtesa, 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 Gemtesa.

Exclusivity Information

Gemtesa holds 1 exclusivities out of which none have expired. Its last outstanding exclusivity is set to expire in 2025. Details of Gemtesa's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
New Chemical Entity Exclusivity(NCE) Dec 23, 2025

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

Gemtesa's Family Patents

Gemtesa has patent protection in a total of 40 countries. It's US patent count contributes only to 14.8% of its total global patent coverage. 10 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 Gemtesa.

Family Patents

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Clinical Trials

Recent Clinical Trials on Gemtesa:

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. Gemtesa(Vibegron) has 3 clinical trials that have been verified in 2024.

Title Lead Sponsor Collaborators Status Phases
A Study of Vibegron in Pediatric Participants 2 Years to Less Than (<) 18 Years of Age With NDO and on CIC Urovant Sciences GmbH RECRUITING
(Jul, 2024)
PHASE2, PHASE3
Study to Evaluate the Efficacy, Safety and Tolerability of Vibegron in Men With Overactive Bladder (OAB) Symptoms on Pharmacological Therapy for Benign Prostatic Hyperplasia (BPH) Urovant Sciences GmbH COMPLETED
(Jun, 2024)
PHASE3
Extension Study of Vibegron in Men With Overactive Bladder (OAB) Symptoms on Pharmacological Therapy for Benign Prostatic Hyperplasia Urovant Sciences GmbH COMPLETED
(Jun, 2024)
PHASE3
Study to Evaluate the Efficacy and Safety of Vibegron Administered Orally for 12 Weeks to Women With Irritable Bowel Syndrome Urovant Sciences GmbH COMPLETED
(Jul, 2021)
PHASE2
A Study to Examine the Safety and Efficacy of a New Drug in Patients With Symptoms of Overactive Bladder (OAB) Urovant Sciences GmbH COMPLETED
(Feb, 2021)
PHASE3
An Extension Study to Examine the Safety and Tolerability of a New Drug in Patients With Symptoms of Overactive Bladder (OAB). Urovant Sciences GmbH COMPLETED
(Feb, 2021)
PHASE3
A Study of the Efficacy and Safety of Vibegron (MK-4618) in Participants With Overactive Bladder (OAB) (MK-4618-008) Merck Sharp & Dohme LLC COMPLETED
(Jan, 2019)
PHASE2
A Study of the Pharmacokinetics and Pharmacodynamics of Vibegron (MK-4618) in Women With Overactive Bladder (MK-4618-004) Merck Sharp & Dohme LLC TERMINATED
(Dec, 2018)
PHASE1
A Single Dose Study of the Pharmacokinetics of Vibegron (MK-4618) in Participants With Renal Insufficiency (MK-4618-014) Merck Sharp & Dohme LLC COMPLETED
(Dec, 2018)
PHASE1
A Single-Dose Study of the Pharmacokinetics of Vibegron (MK-4618) in Adults With Hepatic Insufficiency (MK-4618-013) Merck Sharp & Dohme LLC COMPLETED
(Dec, 2018)
PHASE1




Generic Launch

Generic Release Date:

Gemtesa's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Mar 22, 2040 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Gemtesa Generics:

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





About Gemtesa

Gemtesa is a drug owned by Urovant Sciences Gmbh. It is used for treating overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency. Gemtesa uses Vibegron as an active ingredient. Gemtesa was launched by Urovant in 2020.

Approval Date:

Gemtesa was approved by FDA for market use on 23 December, 2020.

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 Gemtesa is 23 December, 2020, its NCE-1 date is estimated to be 23 December, 2024.

Active Ingredient:

Gemtesa uses Vibegron as the active ingredient. Check out other Drugs and Companies using Vibegron ingredient

Treatment:

Gemtesa is used for treating overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency.

Dosage:

Gemtesa is available in tablet form for oral use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
75MG TABLET Prescription ORAL