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Last Updated: April 1, 2026

ELETRIPTAN HYDROBROMIDE Drug Patent Profile


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

Eletriptan Hydrobromide is a drug marketed by Annora Pharma, Aurobindo Pharma, Chartwell Rx, Mylan, Regcon Holdings, Stevens J, Teva Pharms Usa, Yung Shin Pharm, and Zydus Pharms. and is included in nine NDAs.

The generic ingredient in ELETRIPTAN HYDROBROMIDE is eletriptan hydrobromide. There are twelve drug master file entries for this compound. Twelve suppliers are listed for this compound. Additional details are available on the eletriptan hydrobromide profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Eletriptan Hydrobromide

A generic version of ELETRIPTAN HYDROBROMIDE was approved as eletriptan hydrobromide by ZYDUS PHARMS on June 16th, 2017.

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  • What is the 5 year forecast for ELETRIPTAN HYDROBROMIDE?
  • What are the global sales for ELETRIPTAN HYDROBROMIDE?
  • What is Average Wholesale Price for ELETRIPTAN HYDROBROMIDE?
Drug patent expirations by year for ELETRIPTAN HYDROBROMIDE
Recent Clinical Trials for ELETRIPTAN HYDROBROMIDE

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Technophage, SAPHASE1
VectorB2BPHASE1
PfizerPhase 1

See all ELETRIPTAN HYDROBROMIDE clinical trials

Pharmacology for ELETRIPTAN HYDROBROMIDE
Anatomical Therapeutic Chemical (ATC) Classes for ELETRIPTAN HYDROBROMIDE
Paragraph IV (Patent) Challenges for ELETRIPTAN HYDROBROMIDE
Tradename Dosage Ingredient Strength NDA ANDAs Submitted Submissiondate
RELPAX Tablets eletriptan hydrobromide 20 mg and 40 mg 021016 1 2010-03-29

US Patents and Regulatory Information for ELETRIPTAN HYDROBROMIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Annora Pharma ELETRIPTAN HYDROBROMIDE eletriptan hydrobromide TABLET;ORAL 219143-001 Jul 7, 2025 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Zydus Pharms ELETRIPTAN HYDROBROMIDE eletriptan hydrobromide TABLET;ORAL 206409-002 Jun 16, 2017 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Mylan ELETRIPTAN HYDROBROMIDE eletriptan hydrobromide TABLET;ORAL 205152-001 Aug 11, 2017 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Aurobindo Pharma ELETRIPTAN HYDROBROMIDE eletriptan hydrobromide TABLET;ORAL 210708-002 Jan 15, 2019 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Stevens J ELETRIPTAN HYDROBROMIDE eletriptan hydrobromide TABLET;ORAL 206787-002 May 25, 2018 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

ELETRIPTAN HYDROBROMIDE Market Analysis and Financial Projection

Last updated: February 13, 2026

What Are the Market Dynamics for Eletriptan Hydrobromide?

Eletriptan hydrobromide is a selective serotonin receptor agonist used for acute migraine treatment. Its market is influenced by migraine prevalence, competitive landscape, healthcare policies, and innovation pace.

Market Size and Growth Trends

The global migraine therapeutics market, including eletriptan hydrobromide, was valued at approximately $4.3 billion in 2022. It is projected to grow at a compound annual growth rate (CAGR) of 3.5% from 2023 to 2030, reaching close to $6 billion by 2030 (source: MarketsAndMarkets). This growth relies on increasing migraine incidence and greater awareness.

Regional Market Distribution

North America dominates, accounting for almost 45% of revenue in 2022. The U.S. is the leading market due to high prescription rates, insurance coverage, and healthcare infrastructure. Europe follows at about 25%, with growth driven by aging populations and improved healthcare access. Asia-Pacific exhibits the fastest CAGR (~5%), driven by expanded healthcare penetration and rising migraine awareness.

Competitive Landscape

Eletriptan is marketed by Pfizer under the brand Relpax. It faces competition from other triptans such as sumatriptan, rizatriptan, and zolmitriptan. Generic versions are not yet widespread, providing patent protection until the late 2020s or early 2030s, depending on patent litigations and extensions.

Market share is affected by the drug’s efficacy, side-effect profile, ease of use, and patient preference. Eletriptan’s relatively high bioavailability and re-dosing flexibility give it an edge over some competitors. However, the presence of generics and emerging therapies (e.g., CGRP antagonists) threaten sustained growth.

Policy and Reimbursement Environment

Coverage by major health insurance plans significantly influences sales. In the U.S., Medicare and private insurers reimburse eletriptan with variable co-pays; formulary placement impacts prescribing rates. Stringent regulatory pathways in Europe and other regions demand continuous safety monitoring, affecting timelines and market access.

Innovation and Future Potentials

No major modifications or reformulations of eletriptan are publicly announced. However, research into combination therapies and improved formulations persists. The expansion of digital health tools, remote prescribing, and telemedicine enhances access, especially in underserved regions.


What Is the Financial Trajectory of Eletriptan Hydrobromide?

The financial outlook hinges on revenue growth, patent protection, manufacturing costs, and competitive pressure.

Revenue Forecast

Pfizer generated approximately $750 million in sales from Relpax (eletriptan) in 2022. Sales declined marginally from previous years, attributable to patent exclusivity, competitive pressures, and generic entry threats.

Projected revenues over the next five years average a CAGR of about 1-2%, considered modest due to impending patent expiration and rising generic competition. By 2028, revenue may decline to around $600 million if no new formulations or indications emerge.

Patent and Exclusivity Timeline

Eletriptan’s patent protection in the U.S. extends until 2027-2028, with patent expirations in Europe following shortly after. Patent expiry often results in sharp revenue drops due to generic competition.

Cost Structure and Margins

Manufacturing costs are relatively low, given the small molecule’s synthesis process. Gross margins are high, estimated at 80-85%, driven partly by branding and limited price erosion pre-generics.

Research and development expenses for eletriptan are minimal, as the drug is off-patent in many regions. Marketing and distribution expenditures are streamlined by Pfizer’s existing migraine therapeutic portfolio infrastructure.

Market Entry of Generics and Biosimilars

The entrance of generic eletriptan products post-patent expiration is projected to cause price declines of up to 70% within two years. This will sharply reduce profit margins and overall revenue, unless Pfizer introduces new formulations or indications.

Strategic Investment Outlook

Pfizer’s focus on expanding migraine portfolio and developing personalized medicines suggests that eletriptan's future revenue may depend on integrating with broader migraine management approaches.

New formulations or combination therapies could extend lifecycle or differentiate products, but such developments are not publicly announced as of 2023.


Summary of Market and Financial Outlook

Aspect Status Forecast / Impact
Market Size Valued at $4.3B in 2022 Growth to nearly $6B by 2030
Regional Drivers North America leads; Asia-Pacific fastest growth Continued expansion across regions
Competition Sumatriptan, rizatriptan, generics dominate Price erosion post-patent expiry
Revenue (Pfizer) ~$750 million in 2022 Declining post-2027 due to generics
Patent Expiration 2027-2028 in the U.S. Revenue decline expected post-expiry
Margins 80-85% gross margins Compression expected with generics
R&D & Innovation Minimal ongoing investment Focus on formulations, new indications unlikely

Key Takeaways

  • The eletriptan hydrobromide market relies heavily on migraine prevalence, regional healthcare policies, and patent status.
  • Competitive dynamics favor rapid generic entry upon patent expiration, leading to significant revenue declines.
  • Pfizer’s current revenue is stable but expected to decline marginally post-2027.
  • Strategic diversification and innovation may be necessary for sustained profitability beyond patent expiry.
  • Emerging therapies, like CGRP antagonists, could further challenge eletriptan’s market share.

FAQs

1. When will eletriptan hydrobromide face generic drug competition?
Patent protections in the U.S. are set to expire around 2027-2028, with European and other jurisdictions following shortly after.

2. How does eletriptan compare to other triptans?
Eletriptan has higher bioavailability and flexible dosing, which can lead to better efficacy and tolerability for some patients.

3. What factors could extend the drug’s marketability beyond patent expiry?
Developing new formulations, combination therapies, or gaining approval for additional indications could prolong lifecycle.

4. Are new migraine treatments impacting eletriptan’s market?
Yes; CGRP antagonists are preferred for some patients due to better safety profiles, potentially reducing eletriptan prescriptions.

5. What regions are most attractive for eletriptan sales growth?
North America remains dominant, but Asia-Pacific shows the fastest revenue growth, driven by expanding healthcare access.


References

  1. MarketsAndMarkets. (2022). Migraine therapeutics market report.
  2. Pfizer Inc. annual reports (2022).
  3. GlobalData. (2023). Pharmaceutical industry analysis.
  4. FDA. (2022). Patent information for eletriptan.
  5. IQVIA. (2022). Healthcare industry data.

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