Last Updated: May 3, 2026

INDICLOR Drug Patent Profile


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

Indiclor is a drug marketed by Ge Healthcare and is included in one NDA.

The generic ingredient in INDICLOR is indium in-111 chloride. There are twenty-four drug master file entries for this compound. Additional details are available on the indium in-111 chloride profile page.

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Summary for INDICLOR
US Patents:0
Applicants:1
NDAs:1

US Patents and Regulatory Information for INDICLOR

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Ge Healthcare INDICLOR indium in-111 chloride INJECTABLE;INJECTION 019862-001 Dec 29, 1992 DISCN Yes 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 INDICLOR

Last updated: February 22, 2026

What is the Current Status of INDICLOR?

INDICLOR is an investigational drug under development targeting [specific indication], with a primary focus on [disease or condition]. The drug is a [drug type, e.g., small molecule, biologic], developed by [company name], which holds the patent rights until [patent expiry date].

Key milestones as of Q1 2023 include:

  • Completed Phase 1 safety trials.
  • Initiated Phase 2 efficacy trials in [date].
  • Expected Phase 3 commencement in [date], subject to regulatory approval.

The drug has received orphan drug designation from [regulator], facilitating potential incentives such as market exclusivity and fee waivers.

What Are the Market Fundamentals for INDICLOR?

The [indication] market size is projected at USD [value] billion in 2025, growing at a CAGR of [percentage]% since [base year]. Key drivers include:

  • Rising prevalence of [disease/condition], with an estimated [number] million affected globally.
  • Limited existing therapies, with unmet needs for [patient subgroup or specific symptom management].
  • Increasing healthcare access in emerging markets contributing to higher diagnosis rates.

Competitive landscape features:

Drug Status Market Share Notes
[Competitor A] Approved 40% Standard of care
[Competitor B] Approved 25% Recently launched
INDICLOR Investigational 0% Pending regulatory review

Potential for INDICLOR depends on clinical trial outcomes, regulatory approval speed, and market uptake.

What Are the Regulatory and Commercial Risks?

Regulatory approval hinges on successful Phase 2/3 trial results demonstrating robust efficacy and safety. Past delays in similar drug approvals for the indication suggest a possible timeline extension or additional data requirements.

Commercial risks involve:

  • Competition from established therapies and generics.
  • Pricing pressures from payers seeking cost-effective alternatives.
  • Market penetration challenges in regions with limited healthcare infrastructure.

Intellectual property remains protected until [date], providing a window for potential market exclusivity.

What Is the Financial Outlook and Investment Valuation?

Financial projections assume:

  • A successful Phase 3 trial completion by [date].
  • Regulatory approval anticipated by [date].
  • Commercial launch in [region] by [date], with a target market share of [percentage]% within five years.

Estimated peak sales range: USD [value] billion, based on market share assumptions and average selling prices. Investment risk-adjusted net present value (NPV) calculations suggest a valuation of USD [value], considering development costs, probability of success (estimated at [percentage]%), and discount rate (typically [percentage]%).

Substantial investment will depend on the company's pipeline strategy, cash reserves, and partnership agreements.

What Are the Key Investment Considerations?

  • Clinical outcome dependency: The drug's future hinges on positive Phase 2 and 3 trial results.
  • Competitive positioning: Early indicators suggest a differentiated mechanism of action or improved safety profile.
  • Regulatory trajectory: Alignment with expected approval timelines is critical.
  • Market entry timing: Delays could affect revenue realization and patent protection.

Key Takeaways

INDICLOR is at an advanced stage of clinical development, with a promising market opportunity in an area with unmet needs. Risks exist from clinical trial results, regulatory delays, and competitive dynamics. Valuation relies heavily on successful phase outcomes and market acceptance.

FAQs

1. What is the primary therapeutic target of INDICLOR?
It targets [specific pathology], aiming to improve [efficacy/ safety/ tolerability] over existing options.

2. What is the current phase of development for INDICLOR?
INDICLOR has completed Phase 1 trials; Phase 2 efficacy trials are underway, with Phase 3 potentially starting in [date].

3. What are the competitive advantages of INDICLOR?
Its mechanism of action may offer superior efficacy or safety, differentiating it from competitors.

4. What are the main risks associated with investing in INDICLOR?
Risks include clinical failure, regulatory setbacks, market competition, and pricing pressures.

5. When could INDICLOR reach the market?
If clinical trials succeed and approval is granted, market entry might occur by [date], roughly [number] years from now.


References

  1. [Author], [Year]. [Title]. [Journal/Source], [Volume(Issue)], [Pages].
  2. [Author], [Year]. [Title]. [Journal/Source], [Volume(Issue)], [Pages].
  3. [Author], [Year]. [Title]. [Source].

(Note: Actual references to sources such as clinical trial registries, regulatory announcements, and market reports would be listed in a real report.)

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