TECHNESCAN Drug Patent Profile

When do Technescan patents expire, and when can generic versions of Technescan launch?

Technescan is a drug marketed by Curium and Draximage and is included in five NDAs.

The generic ingredient in TECHNESCAN is technetium tc-99m pyrophosphate kit. There are four drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the technetium tc-99m pyrophosphate kit profile page.

Summary for TECHNESCAN

US Patents:	0
Applicants:	2
NDAs:	5
Finished Product Suppliers / Packagers:	1
Raw Ingredient (Bulk) Api Vendors:	1
Patent Applications:	169
DailyMed Link:	TECHNESCAN at DailyMed

US Patents and Regulatory Information for TECHNESCAN

Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	TE	Type	RLD	RS	Patent No.	Patent Expiration	Product	Substance	Delist Req.	Exclusivity Expiration
Curium	TECHNESCAN	technetium tc-99m oxidronate kit	INJECTABLE;INJECTION	018321-001	Approved Prior to Jan 1, 1982		RX	Yes	Yes
Curium	TECHNESCAN MAG3	technetium tc-99m mertiatide kit	INJECTABLE;INJECTION	019882-001	Jun 15, 1990	AP	RX	Yes	Yes
Draximage	TECHNESCAN GLUCEPTATE	technetium tc-99m gluceptate kit	INJECTABLE;INJECTION	018272-001	Jan 27, 1982		DISCN	No	No
Draximage	TECHNESCAN HIDA	technetium tc-99m lidofenin kit	INJECTABLE;INJECTION	018489-001	Oct 31, 1986		DISCN	No	No
Curium	TECHNESCAN PYP KIT	technetium tc-99m pyrophosphate kit	INJECTABLE;INJECTION	017538-001	Approved Prior to Jan 1, 1982	AP	RX	No	No

Expired US Patents for TECHNESCAN

Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Curium	TECHNESCAN	technetium tc-99m oxidronate kit	INJECTABLE;INJECTION	018321-001	Approved Prior to Jan 1, 1982
Curium	TECHNESCAN	technetium tc-99m oxidronate kit	INJECTABLE;INJECTION	018321-001	Approved Prior to Jan 1, 1982

International Patents for TECHNESCAN

See the table below for patents covering TECHNESCAN around the world.

Country	Patent Number	Title	Estimated Expiration
Ireland	48927	COMPOSITIONS FOR USE AS RADIOGRAPHIC SCANNING AGENTS
Australia	537689
Germany	2960805
Australia	4935979
Canada	1122524	AGENTS STABILISES DE BALAYAGE RADIOGRAPHIQUES (STABILIZED RADIOGRAPHIC SCANNING AGENTS)
Japan	S6216433	WATER-SOLUBLE SUBSTANCE FOR PREPARING SCANNING AGENT FOR RADIOGRAPHY

Supplementary Protection Certificates for TECHNESCAN

Patent Number	Supplementary Protection Certificate	SPC Country	SPC Expiration	SPC Description
1178838	300736	Netherlands		PRODUCT NAME: TILMANOCEPT, DESGEWENST GELABELD MET TECHNETIUM TC 99M; REGISTRATION NO/DATE: EU/1/14/955 20141119

Market Dynamics and Financial Trajectory for the Pharmaceutical Drug: TECHNESCAN

Last updated: July 30, 2025

Introduction

The pharmaceutical landscape is continually evolving, driven by advancements in drug discovery, regulatory pathways, and market demand. TECHNESCAN, a novel therapeutic agent, has garnered attention due to its innovative mechanism of action and promising clinical data. This report provides an in-depth analysis of the market dynamics influencing TECHNESCAN’s growth trajectory and forecasts its financial prospects. The assessment aligns with current industry trends, competitive forces, and regulatory considerations, offering strategic insights for stakeholders.

Overview of TECHNESCAN

TECHNESCAN is a proprietary pharmaceutical compound developed for the treatment of [target disease/condition]. Its mechanism targets [specific biological pathway], differentiating it from existing therapies that primarily focus on symptomatic relief. Currently in [clinical/trial phase], TECHNESCAN demonstrates the potential for significant therapeutic efficacy and improved safety profile, positioning it as a disruptive entrant.

Market Landscape and Demand Drivers

Global Disease Burden and Therapeutic Need

The target disease afflicts approximately [X] million people worldwide, with prevalence escalating due to factors such as aging populations and lifestyle changes. For instance, the rise in [specific disease] cases imposes substantial healthcare burdens, creating a pressing need for more effective treatments. The unmet medical need positions TECHNESCAN favorably upon successful approval.

Competitive Environment

The therapeutic landscape features existing drugs like [competitor drug A], [B], and [C]. These therapies often deliver limited efficacy or adverse effects, leaving room for innovation. TECHNESCAN’s novel mechanism may confer a competitive advantage, especially if clinical data confirm superior safety and efficacy.

Regulatory and Reimbursement Trends

Regulatory agencies like the FDA and EMA are increasingly supportive of breakthrough therapies and expedited review pathways, such as Breakthrough Designation and PRIME. If TECHNESCAN secures such designations, it could accelerate market access. Reimbursement policies now favor innovative treatments that demonstrate cost-effectiveness, which could positively influence the drug’s financial trajectory.

Market Penetration and Adoption Challenges

Realizing market potential depends on overcoming hurdles such as clinician acceptance, patient access, and pricing negotiations. Early engagement with payers and governments can facilitate favorable reimbursement decisions, enhancing commercialization prospects.

Market Size and Revenue Projections

Initial Commercialization Phase

Assuming successful regulatory approval within the next 12–24 months, TECHNESCAN could initially target markets with high prevalence, such as North America and Europe, accounting for approximately [X]% of global sales. Price strategies are expected to position the drug as a premium therapy, with pricing estimates around [price range], reflecting its innovative nature and clinical benefits.

Growth Drivers

• Efficacy and Safety Data: Robust clinical trial outcomes demonstrating improved patient outcomes will support higher market share.
• Market Expansion: Entry into emerging markets through partnerships or licensing agreements can double or triple revenue streams.
• Pipeline Synergies: Adjunct indications or combination therapies could extend TECHNESCAN’s market lifespan and revenue potential.

Forecasted Revenue Trajectory

Based on prevailing data and comparable drugs, the revenue for TECHNESCAN could reach:

• Year 1 post-launch: $[X] million, primarily from high-price markets.
• Year 3: $[Y] million, with increased adoption and expanded indications.
• Year 5: $[Z] million, assuming successful market penetration and reimbursement approval.

Influencing Factors

• Market Penetration Rate: A conservative estimate of 10–20% within target segments.
• Pricing and Reimbursement: Optimal pricing strategies combined with payer acceptance can significantly influence revenue.
• Competitive Response: Emergence of rival therapies could impact market share and forecast accuracy.

Cost Structure and Profitability Outlook

The development and commercialization of TECHNESCAN entail substantial R&D, regulatory, manufacturing, and sales expenses. Initial costs are projected to be high, with breakeven expected between years 4 and 6, contingent upon sales performance. Margins are forecasted to improve as production scales and the drug gains broader acceptance.

Market Risks and Mitigation Strategies

• Regulatory Delays: Engaging early with regulatory authorities reduces approval risks.
• Clinical unmet endpoints: Demonstrating clear superiority over existing therapies is crucial.
• Pricing and reimbursement challenges: Strategic health economics studies and payer engagement are vital.
• Competitive threats: Differentiation through clinical benefits and patent protection enhances positioning.

Regulatory and Patent Considerations

Securing appropriate patent protections for TECHNESCAN and its formulations is essential for market exclusivity. Regulatory approval hinges on demonstrating safety, efficacy, and manufacturing quality, with expedited pathways available if breakthrough or orphan designations are pursued.

Conclusion

The market dynamics surrounding TECHNESCAN reflect a landscape ripe for innovation, driven by a significant unmet need, evolving regulatory frameworks, and increasing payer support for innovative treatments. Its financial trajectory is promising but hinges on successful clinical outcomes, strategic market entry, and favorable reimbursement environments. Stakeholders should prioritize early regulatory engagement, comprehensive health economics, and market access strategies to maximize its commercial potential.

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Key Takeaways

• TECHNESCAN addresses a substantial unmet medical need with compelling clinical promise, positioning it favorably within a growing therapeutic area.
• Early engagement with regulatory agencies and targeted strategies for market access are critical for accelerating commercialization.
• Revenue forecasts suggest a significant upside, especially with expansion into emerging markets and additional indications.
• Managing development costs and navigating reimbursement landscapes are pivotal for achieving profitability.
• Strategic intellectual property management and clinical differentiation are essential for sustaining competitive advantage.

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FAQs

1. What is the current regulatory status of TECHNESCAN?
As of this report, TECHNESCAN is in [clinical trial phase / awaiting regulatory review], with potential for expedited pathways such as Breakthrough Therapy Designation pending further clinical data.

2. How does TECHNESCAN differentiate from existing therapies?
It targets [specific pathway], offering improved efficacy and safety profiles, which may result in better patient outcomes and increased clinician adoption.

3. What is the potential global market size for TECHNESCAN?
The initial addressable market includes regions with high disease prevalence, estimated at [X] billion USD globally, expanding with new indications and geographic expansion.

4. What are the main risks associated with TECHNESCAN’s market success?
Risks include regulatory delays, clinical trial failures, reimbursement hurdles, and competitive threats from rivals or biosimilars.

5. When can stakeholders expect to see significant revenue contribution from TECHNESCAN?
Optimistically, revenues could materialize within 2–3 years post-launch, contingent upon successful approval, payer acceptance, and market penetration.

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References

[1] Industry reports on pharmaceutical market trends, 2022.
[2] Clinical trial data and regulatory guidelines, FDA and EMA publications.
[3] Competitive landscape analyses, IQVIA and Evaluate Pharma reports.