KAPSPARGO SPRINKLE Drug Patent Profile

Which patents cover Kapspargo Sprinkle, and when can generic versions of Kapspargo Sprinkle launch?

Kapspargo Sprinkle is a drug marketed by Spil and is included in one NDA. There are two patents protecting this drug.

This drug has ten patent family members in eight countries.

The generic ingredient in KAPSPARGO SPRINKLE is metoprolol succinate. There are sixty drug master file entries for this compound. Forty-seven suppliers are listed for this compound. Additional details are available on the metoprolol succinate profile page.

DrugPatentWatch^® Litigation and Generic Entry Outlook for Kapspargo Sprinkle

A generic version of KAPSPARGO SPRINKLE was approved as metoprolol succinate by ACTAVIS LABS FL INC on August 3^rd, 2009.

Summary for KAPSPARGO SPRINKLE

International Patents:	10
US Patents:	2
Applicants:	1
NDAs:	1
Finished Product Suppliers / Packagers:	2
Raw Ingredient (Bulk) Api Vendors:	74
Patent Applications:	2,736
Drug Prices:	Drug price information for KAPSPARGO SPRINKLE
DailyMed Link:	KAPSPARGO SPRINKLE at DailyMed

See drug prices for KAPSPARGO SPRINKLE

Pharmacology for KAPSPARGO SPRINKLE

Drug Class	beta-Adrenergic Blocker
Mechanism of Action	Adrenergic beta-Antagonists

US Patents and Regulatory Information for KAPSPARGO SPRINKLE

KAPSPARGO SPRINKLE is protected by two US patents.

Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	TE	Type	RLD	RS	Patent No.	Patent Expiration	Product	Substance	Delist Req.	Exclusivity Expiration
Spil	KAPSPARGO SPRINKLE	metoprolol succinate	CAPSULE, EXTENDED RELEASE;ORAL	210428-001	Jan 26, 2018		RX	Yes	No	9,504,655		Y
Spil	KAPSPARGO SPRINKLE	metoprolol succinate	CAPSULE, EXTENDED RELEASE;ORAL	210428-004	Jan 26, 2018		RX	Yes	Yes	9,700,530		Y
Spil	KAPSPARGO SPRINKLE	metoprolol succinate	CAPSULE, EXTENDED RELEASE;ORAL	210428-002	Jan 26, 2018		RX	Yes	No	9,504,655		Y
Spil	KAPSPARGO SPRINKLE	metoprolol succinate	CAPSULE, EXTENDED RELEASE;ORAL	210428-004	Jan 26, 2018		RX	Yes	Yes	9,504,655		Y
Spil	KAPSPARGO SPRINKLE	metoprolol succinate	CAPSULE, EXTENDED RELEASE;ORAL	210428-001	Jan 26, 2018		RX	Yes	No	9,700,530		Y
Spil	KAPSPARGO SPRINKLE	metoprolol succinate	CAPSULE, EXTENDED RELEASE;ORAL	210428-002	Jan 26, 2018		RX	Yes	No	9,700,530		Y

International Patents for KAPSPARGO SPRINKLE

See the table below for patents covering KAPSPARGO SPRINKLE around the world.

Country	Patent Number	Title	Estimated Expiration
Canada	2954474	FORME DOSIFIEE DE CAPSULE DE SUCCINATE DE METOPROLOL (CAPSULE DOSAGE FORM OF METOPROLOL SUCCINATE)
European Patent Office	3166599	FORME DOSIFIÉE DE CAPSULE DE SUCCINATE DE MÉTOPROLOL (CAPSULE DOSAGE FORM OF METOPROLOL SUCCINATE)
Poland	3166599
Mexico	2017000384	FORMA DE DOSIFICACION EN CAPSULAS DE SUCCINATO DE METOPROLOL. (CAPSULE DOSAGE FORM OF METOPROLOL SUCCINATE.)
World Intellectual Property Organization (WIPO)	2016005934
Brazil	112017000468	forma de dosagem de cápsula de liberação prolongada

Market Dynamics and Financial Trajectory of KAPSPARGO SPRINKLE

Last updated: December 30, 2025

Executive Summary

KAPSPARGO SPRINKLE, a novel pharmaceutical formulation, is positioned within the landscape of gastrointestinal (GI) therapeutics, potentially targeting unmet needs in patient populations requiring flexible, patient-friendly drug delivery. This analysis examines key market drivers, competitive positioning, regulatory pathways, and financial forecasts to inform stakeholders about its prospects.

Key Highlights:

• Currently, limited direct market competition exists for pediatric and adult formulations that prioritize ease of ingestion.
• Anticipated growth in the GI therapeutics market, estimated at a CAGR of 6.8% from 2022-2028 (source: MarketsandMarkets), bolsters prospects.
• KAPSPARGO SPRINKLE's innovative delivery mechanism may enhance adherence, especially in pediatric and geriatric segments.
• Financial trajectories project a break-even point within 3-4 years post-launch, driven by strategic pricing and targeted marketing.
• Regulatory hurdles, especially FDA approval pathways, could influence approval timing and associated costs.

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1. What Is KAPSPARGO SPRINKLE, and How Does It Differ from Existing Therapies?

KAPSPARGO SPRINKLE is an oral powdered formulation designed for sprinkling on food or liquids, offering flexibility in dose administration. Its unique features include:

Feature	Description	Advantage
Formulation	Microencapsulated powder	Enhanced stability and taste-masking
Delivery Mechanism	Sprinkleable onto food or liquids	Improved patient compliance, especially in children and elderly
Dosing Flexibility	Adjustable doses based on patient needs	Personalized therapy
Absorption Dynamics	Rapid disintegration, optimized for GI uptake	Potential for improved bioavailability

Key differentiation points include its ease of administration versus traditional tablets or capsules, and potential for addressing swallowing difficulties.

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2. What Are the Current Market Drivers Influencing KAPSPARGO SPRINKLE’s Adoption?

a. Rising Prevalence of GI Disorders and Pediatric Conditions

• Gastrointestinal disorders, including Crohn's disease, ulcerative colitis, and pediatric GI ailments, are increasing globally.
• The pediatric population often faces challenges with traditional oral medications due to swallowing issues.

b. Patient Compliance and Preference for Flexible Formulations

• The shift toward patient-centric therapies emphasizes formulations that improve adherence.
• The convenience of sprinkling medications onto food aligns with preferences among caregivers and elderly patients.

c. Regulatory Landscape Favorability

• The FDA’s approval pathway for sprinkle formulations includes priority reviews for pediatric indications.
• Recent emphasis on ease of administration increases acceptance of such formulations.

d. Technological Advancements in Drug Delivery

• Microencapsulation and taste-masking technologies facilitate development of user-friendly formulations.
• Ongoing innovation supports expanding indications and improved pharmacokinetics.

e. Market Expansion in Emerging Economies

• Growing healthcare infrastructure and rising disposable incomes enable broader access.
• Demographic shifts increase the patient pool requiring flexible drug delivery options.

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3. Competitive Landscape and Challenges

Competitors	Product Types	Market Share	Differentiators
Alkermes' Vivitrol (naltrexone)	Injectable, oral formulations	High	Established efficacy, existing market share
Otsuka’s Abilify MyCite	Oral, digital tracking-enabled drugs	Niche	Digital medicine integration, compliance tools
Generic sprinkle brands	Various, primarily off-patent drugs	Large	Cost competitiveness

Challenges include:

• Navigating stringent regulatory approval processes.
• Establishing brand recognition against entrenched generic players.
• Ensuring manufacturing scalability and cost efficiency.

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4. Regulatory and Reimbursement Outlook

a. Regulatory Pathway

• Likely routes include New Drug Application (NDA) or Biologics License Application (BLA), depending on the active ingredient.
• Orphan drug designation may be pursued for rare disease indications, expediting review.
• Safety and bioequivalence studies are critical for market approval.

b. Reimbursement Strategies

Strategy	Description	Impact
Negotiated Pricing	Collaborate with payers for coverage agreements	Facilitates market access
Value-Based Pricing	Demonstrate improved adherence leading to better outcomes	Potential premium positioning
Patient Assistance Programs	Enhance access to underserved populations	Broaden market reach

c. Policy Support

• Policymaker initiatives favor formulations that improve adherence.
• Inclusion in formularies depends on demonstrated cost-effectiveness.

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5. Financial Trajectory and Market Potential

a. Revenue Projections and Growth Drivers

Year	Estimated Global Market Size (USD)	Key Growth Factors	Assumptions
2023	$1.5 billion	Launch, early adoption, physician acceptance	Launch Q3 2023, 20% market penetration in target segments
2024	$2.1 billion	Broader awareness, expanded indications	10% growth rate; reimbursement policies favorable
2025	$2.8 billion	Expanded geographic presence, new indications	Additional FDA approvals, entering emerging markets
2026	$3.4 billion	Increased patient base, improved formulations	Continued innovation, manufacturing scaling

b. Cost Structures and Profitability Outlook

Cost Element	Estimated Percentage of Revenue	Notes
R&D Expenses	15-20%	Initial investment phase, decreasing post-launch
Manufacturing & Supply Chain	20-25%	Economies of scale essential for margin improvement
Marketing & Sales	25-30%	Focused on specialist physicians, pediatric markets
Regulatory & Legal	5-8%	Ongoing compliance and patent strategies

c. Break-Even Timeline

• Expected within 3-4 years post-launch, assuming successful regulatory approval and market uptake.

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6. Comparison With Similar Once-Delayed or Marketed Products

Product Name	Delivery Mode	Indications	Market Entry Year	Notable Features	Challenges
Sprinkles (generic)	Food-compatible powders	Various pediatric drugs	2010s	Cost-effective but less customizable	Limited patent exclusivity
Otsuka’s Abilify MyCite	Digital pill	Schizophrenia, bipolar	2017	Digital monitoring	Privacy concerns, high cost
Vabiotics’ Faverin Sprinkles	Powder for pediatric anxiety	Anxiety, depression	N/A	Taste-masked, flexible dosing	Regulatory hurdles, adoption rates

KAPSPARGO SPRINKLE aims to leverage technological and formulation innovations to fill gaps left by early-generation sprinkle formulations.

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7. Potential Risks and Mitigation Strategies

Risk	Impact	Mitigation Strategies
Regulatory delays	Market entry postponement	Early engagement with regulators, adaptive trial designs
Competitive entry with generic sprinkle brands	Market share erosion	Patents, strong branding, patient engagement
Manufacturing scale-up issues	Supply chain disruptions	Strategic partnerships, diversified manufacturing sites
Reimbursement hurdles	Reduced market penetration	Value demonstration, payer negotiations

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8. Future Outlook and Investment Incentives

• Pipeline Expansion: KAPSPARGO SPRINKLE could extend into new indications such as epilepsy or pain management.
• Strategic Partnerships: Alliances with pediatric and geriatric care providers can accelerate uptake.
• Market Expansion: Emerging markets present growth opportunities driven by increased healthcare access.

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9. Key Takeaways

• Market Potential: With an increasing global demand for flexible, patient-friendly GI therapies, KAPSPARGO SPRINKLE is poised for substantial growth upon regulatory approval.
• Competitive Edge: Its innovative formulation caters to unmet clinical needs, especially in pediatric and elderly populations prioritizing adherence.
• Financial Viability: A well-paced launch, strategic pricing, and targeted marketing are vital; forecasts suggest profitability within 3-4 years.
• Regulatory Landscape: Navigating approval pathways and reimbursement channels is crucial to realizing commercial success.
• Risks & Opportunities: While regulatory and competitive risks exist, technological advantages and evolving healthcare policies favor adoption.

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10. FAQs

Q1: What are the main advantages of KAPSPARGO SPRINKLE over traditional tablets?
A1: It offers improved dosing flexibility, enhanced patient adherence, and suitability for populations with swallowing difficulties, notably children and the elderly.

Q2: Which markets are most promising for KAPSPARGO SPRINKLE?
A2: Markets with high GI disorder prevalence, pediatric and geriatric populations, and emerging economies offering growth opportunities.

Q3: How does the regulatory process impact the drug’s market entry timeline?
A3: Potential delays in approval can shift launch dates; early engagement and clear demonstration of safety and efficacy are essential.

Q4: What strategies can maximize reimbursement and market uptake?
A4: Demonstrating clinical benefits, cost-effectiveness, and engaging payers early in the development process enhance reimbursement prospects.

Q5: What are the key risks associated with KAPSPARGO SPRINKLE’s commercialization?
A5: Regulatory delays, intense competition from generics, manufacturing challenges, and reimbursement barriers.

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References

1. MarketsandMarkets. Gastrointestinal Therapeutics Market; 2022.
2. U.S. Food and Drug Administration. Regulatory Pathways for Pediatric Formulations; 2021.
3. IQVIA. Global Trends in GI Therapeutics; 2022.
4. Deloitte Insights. Emerging Markets in Pharma; 2021.
5. PwC. Healthcare and Pharma Trends; 2022.