You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 18, 2025

IMVEXXY Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


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

Imvexxy is a drug marketed by Mayne Pharma and is included in one NDA. There are twenty patents protecting this drug and one Paragraph IV challenge.

This drug has one hundred and sixty-five patent family members in twenty-one countries.

The generic ingredient in IMVEXXY is estradiol. There are seventy-five drug master file entries for this compound. Forty-eight suppliers are listed for this compound. Additional details are available on the estradiol profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Imvexxy

A generic version of IMVEXXY was approved as estradiol by BARR LABS INC on October 22nd, 1997.

  Get Started Free

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for IMVEXXY?
  • What are the global sales for IMVEXXY?
  • What is Average Wholesale Price for IMVEXXY?
Drug patent expirations by year for IMVEXXY
Drug Prices for IMVEXXY

See drug prices for IMVEXXY

Recent Clinical Trials for IMVEXXY

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

SponsorPhase
Teva Pharmaceuticals USAPhase 3
University Hospitals Cleveland Medical CenterPhase 4

See all IMVEXXY clinical trials

Pharmacology for IMVEXXY
Drug ClassEstrogen
Mechanism of ActionEstrogen Receptor Agonists
Paragraph IV (Patent) Challenges for IMVEXXY
Tradename Dosage Ingredient Strength NDA ANDAs Submitted Submissiondate
IMVEXXY Vaginal Inserts estradiol 4 mcg and 10 mcg 208564 1 2019-12-30

US Patents and Regulatory Information for IMVEXXY

IMVEXXY is protected by thirty-four US patents.

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Mayne Pharma IMVEXXY estradiol INSERT;VAGINAL 208564-001 May 29, 2018 RX Yes No 11,116,717 ⤷  Get Started Free Y ⤷  Get Started Free
Mayne Pharma IMVEXXY estradiol INSERT;VAGINAL 208564-002 May 29, 2018 RX Yes Yes 9,180,091 ⤷  Get Started Free Y ⤷  Get Started Free
Mayne Pharma IMVEXXY estradiol INSERT;VAGINAL 208564-002 May 29, 2018 RX Yes Yes 11,116,717 ⤷  Get Started Free Y ⤷  Get Started Free
Mayne Pharma IMVEXXY estradiol INSERT;VAGINAL 208564-001 May 29, 2018 RX Yes No 9,289,382 ⤷  Get Started Free Y ⤷  Get Started Free
Mayne Pharma IMVEXXY estradiol INSERT;VAGINAL 208564-002 May 29, 2018 RX Yes Yes 10,258,630 ⤷  Get Started Free ⤷  Get Started Free
Mayne Pharma IMVEXXY estradiol INSERT;VAGINAL 208564-001 May 29, 2018 RX Yes No 10,806,697 ⤷  Get Started Free Y ⤷  Get Started Free
Mayne Pharma IMVEXXY estradiol INSERT;VAGINAL 208564-001 May 29, 2018 RX Yes No 10,258,630 ⤷  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

International Patents for IMVEXXY

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

Country Patent Number Title Estimated Expiration
Poland 2782584 ⤷  Get Started Free
Mexico 365818 FORMULACIONES Y TERAPIAS DE REEMPLAZO HORMONAL DE COMBINACION NATURALES. (NATURAL COMBINATION HORMONE REPLACEMENT FORMULATIONS AND THERAPIES.) ⤷  Get Started Free
Japan 2018024688 ⤷  Get Started Free
Japan 6656215 ⤷  Get Started Free
Brazil 112014031824 terapias de reposição hormonal transdérmica ⤷  Get Started Free
Mexico 367596 ⤷  Get Started Free
Poland 2861072 ⤷  Get Started Free
>Country >Patent Number >Title >Estimated Expiration

Supplementary Protection Certificates for IMVEXXY

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2861072 2024C/512 Belgium ⤷  Get Started Free PRODUCT NAME: COMPOSITION CONTENANT A LA FOIS DE L'ESTRADIOL, EVENTUELLEMENT SOUS FORME D'UN SEL, HYDRATE OU SOLVATE PHARMACEUTIQUEMENT ACCEPTABLE (Y COMPRIS SOUS FORME HEMIHYDRATEE) ET DE LA PROGESTERONE; AUTHORISATION NUMBER AND DATE: BE582231 20210406
2782584 122021000080 Germany ⤷  Get Started Free PRODUCT NAME: ZUSAMMENSETZUNG, DIE SOWOHL ESTRADIOL (17SS-ESTRADIOL), GEGEBENENFALLS IN FORM EINES PHARMAZEUTISCH ANNEHMBAREN SALZES, HYDRATS ODER SOLVATS DAVON (EINSCHLIESSLICH IN FORM EINES HEMIHYDRATS), ALS AUCH PROGESTERON ENTHAELT; NAT. REGISTRATION NO/DATE: 2205034.00.00 20210924; FIRST REGISTRATION: BELGIEN BE582231 20210406
0770388 09C0018 France ⤷  Get Started Free PRODUCT NAME: ESTRADIOL VALERATE; DIENOGEST; NAT. REGISTRATION NO/DATE: NL35170 20081210; FIRST REGISTRATION: BE327792 20081103
0771217 CA 2006 00038 Denmark ⤷  Get Started Free PRODUCT NAME: ETHINYLESTRADIOL (SOM BETA-CYCLODEXTRIN-CLATHRAT) OG DROSPIRENON; NAT. REG. NO/DATE: 38687 20060627; FIRST REG. NO/DATE: EU RVG 31781 20050804
1453521 15C0050 France ⤷  Get Started Free PRODUCT NAME: ETHINYLESTRADIOL ET MELANGE DE LEVONORGESTREL ET ETHINYLESTRADIOL; NAT. REGISTRATION NO/DATE: NL 42237 20150320; FIRST REGISTRATION: SK - 17/0017/15-S 20150129
1214076 C01214076/01 Switzerland ⤷  Get Started Free PRODUCT NAME: DROSPIRENONE + ETHINYLESTRADIOL; REGISTRATION NUMBER/DATE: SWISSMEDIC 57946 13.06.2008
2782584 301153 Netherlands ⤷  Get Started Free PRODUCT NAME: COMPOSITION CONTAINING BOTH ESTRADIOL (17SS-ESTRADIOL), OPTIONALLY IN THE FORM OF A PHARMACEUTICALLY ACCEPTABLE SALT, HYDRATE OR SOLVATE THEREOF (INCLUDING IN HEMIHYDRATE FORM), AND PROGESTERONE; NATIONAL REGISTRATION NO/DATE: RVG 125821 20210611; FIRST REGISTRATION: BE BE582231 20210406
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description

Market Dynamics and Financial Trajectory for IMVEXXY (Ospemifene) in the Global Pharmaceutical Landscape

Last updated: July 27, 2025


Introduction

IMVEXXY (ospemifene), developed by TherapeuticsMD, represents a significant entrant in the treatment landscape for moderate-to-severe dyspareunia associated with postmenopausal vulvovaginal atrophy (VVA). As a selective estrogen receptor modulator (SERM), IMVEXXY addresses a niche yet growing market segment driven by demographic shifts and increased awareness. This analysis explores the evolving market environment and forecasts the drug's financial trajectory within the broader pharmaceutical industry.


Market Overview and Drivers

The global menopause management market, projected to reach USD 14.2 billion by 2027 with a compound annual growth rate (CAGR) of approximately 6.8%, underpins IMVEXXY’s market potential. The prevalence of menopause-related conditions such as VVA and dyspareunia affects over 50% of postmenopausal women worldwide, translating into a substantial patient population (1).

Key Market Drivers:

  • Demographic Shifts: Aging populations, particularly in North America and Europe, increase the postmenopausal cohort requiring symptomatic relief.
  • Unmet Medical Needs: Limited non-hormonal treatment options with favorable safety profiles bolster demand for therapies like IMVEXXY.
  • Rising Awareness: Education campaigns and physician advocacy improve diagnosis rates, broadening treatment acceptance.
  • Regulatory Approvals: FDA approval of IMVEXXY in 2019, with subsequent expansions, align with favorable regulatory pathways for targeted therapies.

Competitive Landscape

IMVEXXY operates amidst a competitive environment comprising hormonal therapies, local estrogen treatments, and emerging non-hormonal solutions. Key competitors include:

  • Vagifem (estradiol vaginal tablet) and Osphena (ospemifene): Both offer hormonal and non-hormonal options.
  • Replens or vaginal moisturizers: OTC products with broader but less targeted efficacy.
  • Novel non-hormonal agents: Under development, potentially threatening existing drug share.

IMVEXXY’s differentiator is its safety profile — especially its minimal systemic estrogenic effects, making it suitable for women contraindicated for traditional hormone therapy.


Financial Trajectory and Revenue Assumptions

Market Penetration and Adoption

The initial market penetration of IMVEXXY was modest, given the conservative approach to hormone-related therapies and the cautious stance of prescribers. However, recent data suggest growing acceptance, particularly as real-world evidence accumulates indicating favorable safety and efficacy profiles.

Assuming a conservative adoption curve, the following revenue projections are presented:

Year Estimated Prescriptions Average Price per Prescription Revenue (USD millions)
2023 200,000 $350 $70
2024 350,000 $350 $122.5
2025 500,000 $350 $175
2026 750,000 $350 $262.5
2027 1 million $350 $350

Note: Price per prescription factors in negotiated payer discounts and patient co-pays.

Revenue Drivers:

  • Patient Accumulation: Increased diagnosis and prescription rate due to heightened awareness.
  • Pricing Strategy: Payer negotiations may pressure gross prices, although premium positioning can sustain higher margins.
  • Market Expansion: Approval in additional indications or geographic regions, notably Europe and Asia, could significantly escalate revenues.

Regulatory and Marketing Considerations

The success of IMVEXXY hinges on:

  • Regulatory Approvals: Expanding indications or gaining approval in Europe (EMA registration) to tap into broader markets.
  • Reimbursement Policies: Favorable coverage decisions will accelerate uptake.
  • Physician Education: Focused campaigns around safety profile and efficacy will enhance prescriber confidence.
  • Post-Marketing Data: Demonstrating long-term safety will be pivotal in maintaining growth momentum.

Risks and Challenges

  • Market Penetration Risks: Resistance from established hormonal therapies and OTC remedies.
  • Pricing Pressures: Payer pushback could compress margins.
  • Pipeline Competition: Emergence of non-hormonal therapies, including novel agents under clinical trial, could threaten market share.
  • Regulatory Delays: Additional approvals or restrictions could hamper expansion.

Strategic Outlook

TherapeuticsMD's continued investment in clinical trials and market education can bolster IMVEXXY's market share. Strategic partnerships with payers and clinicians, coupled with geographic expansion, can accelerate revenue growth. The evolving landscape suggests a potential compound annual growth rate (CAGR) ranging between 10–15% over the next five years, contingent on regulatory and market dynamics.


Key Market Opportunities

  • Expansion into global markets with burgeoning postmenopausal populations.
  • Development of combination therapies integrating IMVEXXY with other modalities.
  • Targeted marketing campaigns emphasizing safety advantages over traditional HRT.
  • Leveraging digital health tools for patient engagement and adherence.

Conclusion

IMVEXXY's market dynamics are characterized by steady growth fueled by demographic trends, unmet needs, and safety advantages. Financially, the drug exhibits promising trajectories aligning with broader industry trends toward personalized, non-hormonal menopause therapies. Strategic positioning, regulatory navigation, and market penetration efforts will be decisive in realizing its full revenue potential.


Key Takeaways

  • IMVEXXY occupies a niche for postmenopausal women seeking safe, effective treatments for VVA-related dyspareunia.
  • Market growth hinges on demographic trends, increased diagnosis, and favorable regulatory pathways.
  • Revenue forecasts predict a trajectory of steady growth, with potential acceleration upon geographic expansion and indication approvals.
  • Competitive differentiation rests on safety profile, prescriber education, and payer negotiations.
  • Navigating risks related to market acceptance and emerging competitors is crucial for maximizing financial outcomes.

FAQs

1. What distinguishes IMVEXXY from other treatments for postmenopausal VVA?
IMVEXXY’s selective estrogen receptor modulation offers effective symptomatic relief with a minimal systemic estrogenic effect, reducing risks associated with traditional hormone therapy.

2. How is the global market for menopause-related therapies expected to evolve?
Projected to grow at a CAGR of approximately 6.8%, driven by aging populations and rising awareness, creating expansive opportunities for targeted therapies like IMVEXXY.

3. What challenges does IMVEXXY face in capturing market share?
Established therapies, payer negotiations, regulatory barriers, and competition from emerging non-hormonal agents pose significant hurdles.

4. Are there plans for IMVEXXY’s approval in markets outside the U.S.?
Yes, regulatory submissions in Europe and Asia are underway, which could substantially enhance its global revenue potential.

5. What strategies could accelerate IMVEXXY’s financial growth?
Broadening indications, expanding geographic reach, emphasizing safety benefits, and forming strategic partnerships with payers and healthcare institutions.


Sources:
[1] Global Menopause Management Market Report, 2021-2027.
[2] FDA approval archives for IMVEXXY, 2019.
[3] Industry reports on postmenopausal therapy trends.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.