Overactive Bladder Pipeline Outlook Report 2025: Detailed Analysis of Novel Therapeutics, Key Players, and Strategic Developments in SMA Market

DelveInsight's "Overactive Bladder Pipeline Insights 2025" report provides comprehensive insights about 15+ companies and 15+ pipeline drugs in Overactive Bladder pipeline landscape. It covers the Overactive Bladder pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Overactive Bladder pipeline therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

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Key Takeaways from the Overactive Bladder Pipeline Report
• In January 2025, Imbrium Therapeutics L.P. ("Imbrium"), a subsidiary of Purdue Pharma L.P. ("Purdue"), announced results from a Phase Ib clinical signal detection study evaluating the safety and efficacy of the novel investigational treatmentsunobinop in patients with overactive bladder syndrome.
• DelveInsight's Overactive Bladder pipeline report depicts a robust space with 15+ active players working to develop 15+ pipeline therapies for Overactive Bladder treatment.
• The leading Overactive Bladder Companies such as Dong-A ST Co., Ltd., AbbVie/Medytox, Urovant Sciences, Taiho Pharma, Velicept Therapeutics and others.
• Promising Overactive Bladder Pipeline Therapies such as GSK1358820, YM178, Fesoterodine 8 mg, Vibegron, Tolterodine ER, Solifenacin Succinate, Oxybutynin chloride OROS, VESIcare®, Fesoterodine, and others.

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Overactive Bladder Emerging Drugs Profile
• Neuronox: AbbVie/Medytox
Neuronox, an acetylcholine inhibitor is being developed by Medy-Tox for the treatment of the Overactive Bladder. The active ingredients involve Clostridium botulinum toxin type A. It is currently in the phase III stage of development. In September 2020, US drugmaker Allergan entered into a license agreement with South Korea's Medytox under the terms of which, on closing, Allergan would pay Medytox an upfront of USD 65 million and Medytox would grant Allergan exclusive rights, worldwide outside of Korea, to develop and, if approved, commercialise certain neurotoxin product candidates currently in development, including a potential liquid-injectable product. In May 2020, AbbVie announced that it had finished its acquisition of Allergan plc following receipt of regulatory approval from all government authorities needed by the transaction agreement and approval by the Irish High Court.

• URO-902: Urovant Sciences
Urovant Sciences is developing URO-902 for the treatment of the Overactive Bladder. URO-902 has the potential to be the first gene therapy for OAB patients. This innovative treatment has the capability to tackle an unmet need for patients who have failed oral pharmacologic therapies and are concerned with potential urinary retention or surgical interventions pertinent to existing third-line OAB treatments. It is currently in the phase II stage of development.

The Overactive Bladder Pipeline report provides insights into
• The report provides detailed insights about companies that are developing therapies for the treatment of Overactive Bladder with aggregate therapies developed by each company for the same.
• It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Overactive Bladder Treatment.
• Overactive Bladder Companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
• Overactive Bladder Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type.
• Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Overactive Bladder market.

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Overactive Bladder Companies
Dong-A ST Co., Ltd., AbbVie/Medytox, Urovant Sciences, Taiho Pharma, Velicept Therapeutics and others.

Overactive Bladder Pipeline Report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
• Intra-articular
• Intraocular
• Intrathecal
• Intravenous
• Ophthalmic
• Oral
• Parenteral
• Subcutaneous
• Topical
• Transdermal

Overactive Bladder Products have been categorized under various Molecule types such as
• Oligonucleotide
• Peptide
• Small molecule

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Scope of the Overactive Bladder Pipeline Report
• Coverage- Global
• Overactive Bladder Companies- Dong-A ST Co., Ltd., AbbVie/Medytox, Urovant Sciences, Taiho Pharma, Velicept Therapeutics and others.
• Overactive Bladder Pipeline Therapies- GSK1358820, YM178, Fesoterodine 8 mg, Vibegron, Tolterodine ER, Solifenacin Succinate, Oxybutynin chloride OROS, VESIcare®, Fesoterodine, and others.
• Overactive Bladder Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
• Overactive Bladder Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III

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Table of Contents
1. Introduction
2. Executive Summary
3. Overactive Bladder: Overview
4. Pipeline Therapeutics
5. Therapeutic Assessment
6. Overactive Bladder- DelveInsight's Analytical Perspective
7. Late Stage Products (Phase III)
8. Neuronox: AbbVie/Medytox
9. Mid Stage Products (Phase II)
10. URO-902: Sumitovant Biopharma
11. Early Stage Products (Phase I)
12. Drug Name: Company Name
13. Preclinical and Discovery Stage Products
14. Drug Name: Company Name
15. Inactive Products
16. Overactive Bladder Key Companies
17. Overactive Bladder Key Products
18. Overactive Bladder- Unmet Needs
19. Overactive Bladder- Market Drivers and Barriers
20. Overactive Bladder- Future Perspectives and Conclusion
21. Overactive Bladder Analyst Views
22. Overactive Bladder Key Companies
23. Appendix

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This release was published on openPR.