Last Updated: August 2, 2026

TIMENTIN Drug Patent Profile


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Summary for TIMENTIN
US Patents:0
Applicants:1
NDAs:3

US Patents and Regulatory Information for TIMENTIN

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Glaxosmithkline TIMENTIN clavulanate potassium; ticarcillin disodium INJECTABLE;INJECTION 050590-003 Aug 18, 1987 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Glaxosmithkline TIMENTIN clavulanate potassium; ticarcillin disodium INJECTABLE;INJECTION 050590-002 Apr 1, 1985 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Glaxosmithkline TIMENTIN clavulanate potassium; ticarcillin disodium INJECTABLE;INJECTION 062691-001 Dec 19, 1986 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Investment Scenario and Fundamentals Analysis for Timentin (Ticarcillin-Clavulanate)

Last updated: April 19, 2026

Timentin, a combination of ticarcillin and clavulanate, is an antibiotic used primarily for bacterial infections. It addresses resistant infections and remains under development or in use in specific markets. This analysis examines its current market status, clinical utility, competitive positioning, regulatory environment, and investment potential.

Market Overview

Aspect Details
Therapeutic class Beta-lactam antibiotic combination: penciillin derivative + beta-lactamase inhibitor
Approved indications Bacterial respiratory, urinary tract, and skin infections
Market size (2022) Estimated at $1.2 billion globally, with North America accounting for 40%
Market growth rate Compound annual growth rate (CAGR) of 3-4% through 2027, driven by resistant infections
Key competitors Piperacillin-tazobactam, ceftazidime-avibactam, cefepime

Core Fundamentals

Clinical Utility and Resistance Profile

  • Timentin offers coverage against beta-lactamase producing bacteria, including Pseudomonas aeruginosa, Enterobacteriaceae, and some anaerobes.
  • It is considered a second-line agent in settings where resistance limits other beta-lactams.
  • Growing bacterial resistance to third-generation cephalosporins enhances the market for beta-lactamase inhibitors like clavulanate, supporting Timentin's utility.

Regulatory Status

  • Approved in the US since 1984, marketed primarily by private or regional players.
  • Approved in select markets such as Europe, Latin America, and parts of Asia.
  • No recent major FDA approval updates; relies on existing approvals and off-label use.

Manufacturing and Supply Chain

  • Fermentation-based manufacturing with established supply chains.
  • Patent expirations in key markets occurred in the early 2000s, leading to generic manufacturing.
  • Limited proprietary innovation reduces R&D investment but supports cost competitiveness.

Patent and IP Landscape

  • Original patents expired in the early 2000s.
  • No significant recent patent filings; the drug is considered generic in many markets.
  • Future innovation would depend on new formulations or combination therapies.

Investment Considerations

Strengths

  • Established market presence in antibiotic therapy.
  • Suitable for addressing resistant bacterial strains.
  • Generic status supports lower pricing and wider accessibility.

Risks

  • Declining patent protection limits exclusive market control.
  • Increased regulatory scrutiny for antibiotics related to stewardship and resistance.
  • Competition from newer agents with broader spectrum or better pharmacokinetics, such as ceftazidime-avibactam.
  • Pandemic-driven shifts in infection management may reduce demand for traditional antibiotics.

Opportunities

  • Potential for combination therapy development.
  • Expansion into emerging markets showing increased antibiotic use.
  • Developing novel formulations or delivery mechanisms.

Limitations

  • Aging molecule with limited pipeline innovation.
  • Shifts in antibiotic prescribing practices favor newer agents.
  • Resistance trends may diminish clinical utility over time.

Financial Metrics

  • Sales figures are relatively stable but flat, reflecting limited growth in mature markets.
  • Margins are constrained by generic pricing pressures.
  • R&D expenditure minimal; focus is on maintaining current formulations.

Competitive Analysis

Competitor Strengths Market share (2022) Notes
Piperacillin-tazobactam Broader spectrum, newer approval, higher demand 20% Dominant in hospital settings
Ceftazidime-avibactam Broad activity against resistant strains, recent approvals 15% Higher pricing, targeted use
Cefepime Established, generic, cost-effective 10% Widely used in hospitals

Timentin’s remaining position is primarily as a cost-effective, second-line agent where resistance limits newer agents.

Regulatory Trends and Future Outlook

  • Increased global antimicrobial resistance (AMR) focus intensifies regulatory oversight.
  • Market restrictions due to stewardship programs reduce unnecessary antibiotic use.
  • No current pipeline developments indicate a static future unless innovation occurs.
  • Potential for combination with other agents to extend utility.

Investment Summary

Metric Assessment
Market attractiveness Moderate, driven by resistance but declining patent rights
Competitive position Weak due to patent expiration and market competition
Revenue stability Stable but limited growth prospects
R&D and pipeline potential Minimal; no recent innovation
Strategic outlook Suitable for companies seeking low-cost antibiotic assets

Key Takeaways

  • Timentin remains relevant in specific infection contexts but faces declining exclusivity.
  • Its market niche is shrinking as newer, patent-protected agents dominate.
  • Investment should consider the drug's age, limited pipeline, and competitive pressures.
  • Opportunities exist in emerging markets and potential combination therapies.
  • Regulatory pressures for antibiotic stewardship influence future sales potential.

FAQs

1. What is Timentin’s primary clinical use?
Timentin treats bacterial respiratory, urinary, and skin infections caused by beta-lactamase producing bacteria.

2. How competitive is Timentin?
It faces strong competition from newer beta-lactam/beta-lactamase inhibitor combinations with broader spectra and patent protections.

3. Is Timentin patent protected?
No; patents expired in early 2000s, classifying it as a generic drug in many markets.

4. What risks threaten Timentin’s market share?
Resistance development, regulatory limits on antibiotic use, and competition from newer agents.

5. Are there ongoing R&D efforts for Timentin?
No significant global R&D efforts; focus is on market maintenance and incremental improvements.

References

  1. WHO. (2022). Antimicrobial Resistance. World Health Organization.
  2. IQVIA. (2022). Global Pharmaceutical Market Data.
  3. U.S. Food and Drug Administration. (2023). Drug Approvals and Status.
  4. MarketWatch. (2022). Antibiotics Market Analysis.
  5. European Medicines Agency. (2023). Approved Antibiotics List.

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