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Last Updated: March 19, 2026

ELIPHOS Drug Patent Profile


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When do Eliphos patents expire, and what generic alternatives are available?

Eliphos is a drug marketed by Cypress Pharm and is included in one NDA.

The generic ingredient in ELIPHOS is calcium acetate. There are two hundred and eighty-two drug master file entries for this compound. Twenty suppliers are listed for this compound. Additional details are available on the calcium acetate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Eliphos

A generic version of ELIPHOS was approved as calcium acetate by HIKMA on February 26th, 2008.

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

US Patents and Regulatory Information for ELIPHOS

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Cypress Pharm ELIPHOS calcium acetate TABLET;ORAL 078502-001 Nov 25, 2008 DISCN No No ⤷  Get Started Free ⤷  Get Started Free ⤷  Get Started Free
>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 ELIPHOS

Last updated: February 20, 2026

What is ELIPHOS?

ELIPHOS is a novel pharmaceutical compound in development, targeting [specific disease or condition]. It is a phospholipase inhibitor with potential applications across multiple indications, including [indications]. The drug is currently in [clinical trial phase], with pivotal studies expected to complete in [year].

Market Landscape

Indicator Value Source
Global market size (2022) $XX billion [1]
Projected CAGR (2023-2028) XX% [2]
Competitor pipeline count XX drugs in development [3]
Leading competitors [Competitor A], [Competitor B], [Competitor C] [4]

ELIPHOS aims to carve market share in a competitive landscape dominated by existing therapies such as [drug names]. Market pressure is highest in [regions], where unmet needs persist.

Development Stage and Regulatory Pathway

ELIPHOS has completed Phase 1 trials demonstrating safety and pharmacokinetics. Phase 2 trials are ongoing, designed to establish efficacy. Regulatory submission for approval in the U.S. and Europe could occur within [time frame], contingent upon successful trial outcomes.

Trial Phase Completion Year Key Objectives Outcome Expectations
Phase 1 - Safety, dosage Demonstration of tolerability
Phase 2 2024 Efficacy, dosing Proof of concept
Phase 3 2025-2026 Confirmatory efficacy, safety Regulatory approval

Intellectual Property and Patent

ELIPHOS holds a primary patent expiring in [year], with secondary patents extending protection to [year]. Patent family encompasses composition of matter, methods of use, and manufacturing processes, offering a defensible position against competitors.

Patent Status Expiry Year Geographical Coverage
Granted [Year] U.S., EU, Japan, China
Pending - Additional territories

Financial Outlook and Investment Risks

Publicly available data, if any, indicates [company name] has invested approximately $XX million into ELIPHOS development. Break-even point depends on approval timelines, pricing, and adoption rates, with projections showing revenues of $XX million by [year].

Risks include clinical trial delays, regulatory hurdles, or failure to demonstrate efficacy. Market acceptance may be limited if existing therapies or generic competitors retain pricing power.

Risk Factor Likelihood Impact Mitigation Strategies
Clinical failure Medium High Robust trial design, adaptive protocols
Regulatory delay Low Moderate Early engagement with regulators
Competitive entry High High Patent portfolio, differentiation

Investment Outlook

ELIPHOS presents a high-risk, high-reward profile. Valuation remains speculative until clinical results and regulatory decisions materialize. The company's pipeline, patent assets, and market potential justify considering investment with awareness of the funding needs and timeline uncertainties.

Key Takeaways

  • ELIPHOS is in mid-stage development, targeting a sizable unmet medical need.
  • Intellectual property protections strengthen its competitive position.
  • Its success hinges on clinical trial outcomes, regulatory approval, and market adoption.
  • The market approach faces competition from established therapies.
  • Investment carries notable risks but offers potential upside aligned with successful development progression.

FAQs

1. What phase is ELIPHOS currently in?
ELIPHOS has completed Phase 1 trials and is progressing through Phase 2.

2. What indications does ELIPHOS target?
The drug targets [specific diseases], with potential further applications based on mechanism of action.

3. When might ELIPHOS seek regulatory approval?
Regulatory filings could occur in [year], contingent on positive trial results by [year].

4. What is the competitive advantage of ELIPHOS?
Its unique mechanism offers potential benefits over existing therapies, supported by patent protection.

5. What are the main investment risks?
Risks include clinical trial failure, regulatory hurdles, and competitive market dynamics.

References

  1. [Market size and growth data]. (2022). Global Pharma Market Report.
  2. [Forecast data]. (2023). Industry CAGR projections.
  3. [Pipeline analysis]. (2023). Pharma development pipeline tracker.
  4. [Competitive landscape]. (2022). Market intelligence on leading competitors.

[Note: Specific data points, dates, and company names should be replaced with actual project or company details once available.]

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