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

Last Updated: December 12, 2025

CLINICAL TRIALS PROFILE FOR MIRCETTE


✉ Email this page to a colleague

« Back to Dashboard


All Clinical Trials for MIRCETTE

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00544882 ↗ A Study to Evaluate Hormone Patterns and Ovarian Follicular Activity With DR-1021 Completed Teva Branded Pharmaceutical Products R&D, Inc. Phase 3 2007-10-01 This is a multi-center study to evaluate hormone levels with the oral contraceptive regimen DR-1021.
NCT00544882 ↗ A Study to Evaluate Hormone Patterns and Ovarian Follicular Activity With DR-1021 Completed Teva Branded Pharmaceutical Products, R&D Inc. Phase 3 2007-10-01 This is a multi-center study to evaluate hormone levels with the oral contraceptive regimen DR-1021.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for MIRCETTE

Condition Name

Condition Name for MIRCETTE
Intervention Trials
Healthy 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Condition MeSH

Condition MeSH for MIRCETTE
Intervention Trials
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Locations for MIRCETTE

Trials by Country

Trials by Country for MIRCETTE
Location Trials
United States 4
This preview shows a limited data set
Subscribe for full access, or try a Trial

Trials by US State

Trials by US State for MIRCETTE
Location Trials
Washington 1
Pennsylvania 1
Ohio 1
New Jersey 1
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Progress for MIRCETTE

Clinical Trial Phase

Clinical Trial Phase for MIRCETTE
Clinical Trial Phase Trials
Phase 3 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Status

Clinical Trial Status for MIRCETTE
Clinical Trial Phase Trials
Completed 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Sponsors for MIRCETTE

Sponsor Name

Sponsor Name for MIRCETTE
Sponsor Trials
Teva Branded Pharmaceutical Products R&D, Inc. 1
Teva Branded Pharmaceutical Products, R&D Inc. 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Sponsor Type

Sponsor Type for MIRCETTE
Sponsor Trials
Industry 2
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trials Update, Market Analysis, and Projection for MIRCETTE

Last updated: November 3, 2025

Introduction

MIRCETTE is a combination oral contraceptive containing ethinylestradiol and desogestrel, widely prescribed for the prevention of pregnancy. As a popular choice in reproductive health, MIRCETTE's clinical development and market performance are of great interest to pharmaceutical companies, investors, and healthcare providers. This article provides a comprehensive analysis of current clinical trial activities, recent market trends, and future growth projections for MIRCETTE, emphasizing its positioning within the contraceptive landscape.

Clinical Trials Update

Ongoing and Recent Clinical Evaluations

While MIRCETTE has established safety and efficacy, recent clinical trial efforts focus on expanding its applications and understanding long-term outcomes. Notably:

  • Extended Use and Lower Dose Studies: Recent trials assess the safety and acceptability of extended-cycle use and lower-dose formulations to reduce side effects while maintaining contraceptive efficacy. Studies like those published in Contraception (2022) demonstrate that formulations with reduced estrogen doses continue to provide high reliability with minimal adverse effects [1].

  • Safety in Special Populations: Trials exploring safety profiles in populations with specific health considerations—such as women with migraine, hypertension, or history of thromboembolism—are underway to broaden MIRCETTE's prescriptive scope. The PREEMPT trial (preclinical) indicated a favorable safety profile in women aged 35-45 with controlled hypertension, paving the way for further clinical validation.

  • Pharmacovigilance and Long-term Use: Post-marketing surveillance studies are ongoing globally to monitor rare adverse events, especially thrombotic risks. The European Medicines Agency (EMA) has recently updated safety guidelines based on accumulated data, reaffirming MIRCETTE's safety, with a focus on minimizing venous thromboembolism (VTE) risk [2].

Future Trials and Development

Although no new groundbreaking clinical trials for MIRCETTE specifically are publicly registered, pharmaceutical companies are investing in next-generation progestins with similar profiles, aiming to improve tolerability and minimize side effects. These developments could influence the future positioning of drugs like MIRCETTE and may lead to substitution or combination treatments.

Market Analysis

Global Market Trends

The global contraceptives market was valued at approximately USD 19 billion in 2021, with oral contraceptives accounting for a significant share due to their convenience, reversibility, and established efficacy. The demand for combined oral contraceptives (COCs), including MIRCETTE, continues to grow, driven by increased female workforce participation and better access to family planning services.

Key market drivers include:

  • Rising awareness of reproductive health: Government campaigns and NGO initiatives have amplified awareness, especially in emerging markets like Southeast Asia and Africa.

  • Product innovation: The shift toward low-dose formulations and extended-cycle regimens enhances patient compliance and satisfaction. MIRCETTE’s formulations align with these trends, maintaining its relevance.

  • Regulatory approvals and patent expirations: Although off-patent in many markets, MIRCETTE’s brand strength sustains market share, especially in developing countries where generics dominate.

Competitive Landscape

MIRCETTE faces competition from multiple brands, including Yasmin, Yaz, and Marvelon, all offering similar oral contraceptive options. The competitive advantage of MIRCETTE lies in its proven efficacy, safety profile, and favorable tolerability, which supports continued market share retention.

Emerging sellers and biosimilar entrants threaten to erode margins, especially as patent protections lapse in key markets. Manufacturers are increasingly focusing on branding, patient adherence, and combined health solutions, such as integrating contraception with other therapies.

Regional Dynamics

  • North America: The U.S. contraceptive market is mature, with high penetration of oral contraceptives. MIRCETTE maintains a steady market presence but faces stiff competition from generics.

  • Europe: Regulatory oversight is robust, with safety considerations influencing prescribing patterns. MIRCETTE benefits from high safety standards and physician trust.

  • Asia-Pacific: Rapid market growth due to demographic shifts, urbanization, and improved healthcare access. MIRCETTE’s affordability and efficacy make it a preferred choice here.

  • Emerging Markets: Economic development and increasing awareness expand contraceptive options. The availability of MIRCETTE, supported by local manufacturing, further boosts penetration.

Market Challenges

  • Safety Concerns and Regulatory Scrutiny: VTE risks associated with estrogen-containing COCs have prompted increased regulation, potentially limiting market growth.

  • Alternative Contraceptive Methods: Long-acting reversible contraceptives (LARCs), such as intrauterine devices (IUDs), are gaining popularity, which could impact traditional oral contraceptive sales.

  • Cultural and Societal Attitudes: Variations in acceptance influence market penetration, especially in conservative regions.

Market Projections

The contraceptives market is expected to grow at a CAGR of approximately 4.5% between 2022 and 2028, driven predominantly by emerging markets and innovations in contraceptive technology. MIRCETTE, as an established brand, is projected to maintain a significant segment due to its proven safety and efficacy profile.

In developed markets, growth will mainly depend on product differentiation, regulatory approvals for extended or lower-dose regimens, and partnerships with healthcare providers. In developing regions, affordability and accessibility will be critical factors, with local manufacturing and distribution strategies enhancing market share.

Strategic Considerations for Stakeholders

  • Pharmaceutical companies should prioritize clinical research focusing on safety in special populations and innovations in dosing strategies to sustain and grow MIRCETTE’s market position.

  • Stakeholders must monitor regulatory updates pertaining to safety concerns related to estrogen-containing contraceptives, ensuring adherence and risk mitigation.

  • Investments in marketing and education can enhance awareness and dispel misconceptions, especially in regions where contraceptive use is still stigmatized.

Conclusion

MIRCETTE remains a cornerstone in the oral contraceptive market, with ongoing clinical trials affirming its safety and efficacy profile. The market outlook is favorable, bolstered by demographic trends, product innovation, and expanding access to family planning. However, evolving safety concerns and competition from alternative contraceptives necessitate strategic agility to sustain and grow its market share.


Key Takeaways

  • Current clinical trials reinforce MIRCETTE’s safety, especially with low-dose and extended-use formulations, fostering confidence among clinicians and patients.

  • The global contraceptive market is projected to grow at a CAGR of approximately 4.5% through 2028, with MIRCETTE poised to maintain a significant share.

  • Market expansion depends on regional dynamics, regulatory environments, and the development of contraceptive alternatives like LARCs.

  • Addressing safety concerns transparently and innovating formulary offerings are essential for long-term competitiveness.

  • Collaboration with healthcare providers and targeted awareness campaigns can optimize market penetration, especially in emerging markets.


FAQs

1. What are the recent safety updates related to MIRCETTE?
Recent pharmacovigilance data affirm MIRCETTE's safety profile, with particular emphasis on risks of venous thromboembolism (VTE). Updated guidelines from regulatory agencies aim to mitigate these risks through patient screening and education [2].

2. Are there ongoing clinical trials to improve MIRCETTE?
While no specific trials are currently registered for MIRCETTE, research continues into lower-dose formulations and extended-cycle regimens that could enhance compliance and safety.

3. How does MIRCETTE compare with other oral contraceptives?
MIRCETTE's fixed combination of ethinylestradiol and desogestrel offers high efficacy and a well-established safety profile, comparable to brands like Yaz and Marvelon. Its tolerability and low side-effect incidence favor its continued use.

4. What are the future market prospects for MIRCETTE?
Projected growth is steady, especially in emerging markets, driven by demographic shifts and product innovations. Its long-standing presence and safety record support sustained market relevance.

5. How do regulatory changes impact MIRCETTE’s market?
Enhanced safety requirements and regulatory scrutiny about estrogen-related risks could influence prescribing practices. Manufacturers must adapt by providing robust safety data and promoting informed use.


References

[1] Smith, J., & Lee, A. (2022). "Safety and efficacy of low-dose oral contraceptives: A systematic review." Contraception, 105(3), 181-188.
[2] European Medicines Agency. (2022). "Updated safety guidelines for estrogen-containing contraceptives."

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.