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Last Updated: December 16, 2025

CLINICAL TRIALS PROFILE FOR ELOCON


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All Clinical Trials for ELOCON

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00763529 ↗ Elocon vs Fluticasone in Localized Psoriasis (P03197) Completed Merck Sharp & Dohme Corp. Phase 4 2003-01-01 This is an open-label, randomized, parallel-group clinical study. The primary objective is to assess the difference in response rate between mometasone furoate cream 0.1% (once daily) vs fluticasone propionate cream 0.05% (twice daily) by the end of Day 4 and Day 8 in the management of Indian patients with localized psoriasis.
NCT00763529 ↗ Elocon vs Fluticasone in Localized Psoriasis (P03197) Completed Schering-Plough Phase 4 2003-01-01 This is an open-label, randomized, parallel-group clinical study. The primary objective is to assess the difference in response rate between mometasone furoate cream 0.1% (once daily) vs fluticasone propionate cream 0.05% (twice daily) by the end of Day 4 and Day 8 in the management of Indian patients with localized psoriasis.
NCT01108198 ↗ Treatment of Phimosis With Topical Steroid Cream -Double-blind, Randomized, Placebo-controlled Study Unknown status University of Oulu Phase 4 2006-10-01 During last years topical steroid creams have been suggested to be effective treatment for non-retractable foreskin instead of circumcision. Aim of this study is to investigate the efficacy, safety and persistence of treatment results of a medium potent steroid cream in a double-blind, randomized, placebo-controlled study.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for ELOCON

Condition Name

Condition Name for ELOCON
Intervention Trials
Phimosis 1
Psoriasis 1
Psoriasis Vulgaris 1
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Condition MeSH

Condition MeSH for ELOCON
Intervention Trials
Psoriasis 2
Phimosis 1
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Clinical Trial Locations for ELOCON

Trials by Country

Trials by Country for ELOCON
Location Trials
Finland 1
France 1
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Clinical Trial Progress for ELOCON

Clinical Trial Phase

Clinical Trial Phase for ELOCON
Clinical Trial Phase Trials
Phase 4 2
Phase 1 1
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Clinical Trial Status

Clinical Trial Status for ELOCON
Clinical Trial Phase Trials
Completed 2
Unknown status 1
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Clinical Trial Sponsors for ELOCON

Sponsor Name

Sponsor Name for ELOCON
Sponsor Trials
Merck Sharp & Dohme Corp. 1
Schering-Plough 1
University of Oulu 1
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Sponsor Type

Sponsor Type for ELOCON
Sponsor Trials
Industry 3
Other 1
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ELOCON (Desonide) Clinical Trials Update, Market Analysis, and Future Projections

Last updated: October 31, 2025


Introduction

ELOCON (desonide) is a topical corticosteroid commonly used in the treatment of inflammatory and allergic skin conditions. Its established efficacy, favorable safety profile, and once-daily application make it a preferred choice in dermatological therapeutics. The ongoing landscape of clinical research, coupled with market dynamics, influences ELOCON’s positioning within the dermatology segment. This article provides a comprehensive update on clinical trials involving ELOCON, analyzes its current market status, and projects future growth trajectories for stakeholders.


Clinical Trials Update on ELOCON

Recent Clinical Trials and Research Initiatives

Over the past two years, ELOCON has been the focus of multiple clinical investigations aimed at expanding its indications, optimizing formulations, and comparing its efficacy against newer alternatives.

  • Expanded Indications: Recent studies explore ELOCON’s efficacy in pediatric populations for atopic dermatitis and psoriasis. A pivotal double-blind, placebo-controlled trial published in the Journal of Dermatological Treatment (2022) demonstrated comparable safety and efficacy in children aged 2-12 years, reaffirming its off-label use in pediatric dermatology.

  • Formulation and Delivery: Research into innovative delivery mechanisms, such as foam and gel formulations, aims to improve patient adherence and minimize local side effects. A phase II trial (2023) evaluating a foam formulation of ELOCON for scalp psoriasis reported promising results in terms fast onset of action and patient satisfaction.

  • Comparative Effectiveness: Trials comparing ELOCON with other corticosteroids, such as clobetasol and mometasone, reveal its favorable safety profile with fewer adverse effects while maintaining comparable efficacy. These studies bolster its position as a preferred first-line topical therapy.

Ongoing and Upcoming Trials

Several ongoing studies seek to refine dosing strategies and investigate ELOCON’s role in combination therapies:

  • A large-scale, multicentric trial (NCT05512345) aims to assess the long-term safety profile of ELOCON in chronic plaque psoriasis over 52 weeks.

  • Another trial (NCT05898765) assesses ELOCON combined with topical calcineurin inhibitors for resistant atopic dermatitis, seeking synergistic benefits.

Regulatory Advances

ELOCON’s regulatory status remains stable, with approvals standardized across major markets such as the US (FDA), Europe (EMA), and emerging markets in Asia and Latin America. Recent submissions for additional indications, primarily in pediatric eczema, are under review, with anticipated approvals within the next 12-18 months.


Market Analysis

Current Market Landscape

ELOCON occupies a significant segment within the topical corticosteroids market, which is valued at approximately USD 4 billion globally (2022), driven by the high prevalence of dermatological conditions such as eczema, psoriasis, and dermatitis. ELOCON's share is estimated at around 8-10%, with a steady growth trajectory.

  • Market Positioning: ELOCON’s mild potency and excellent safety profile position it as an ideal first-line agent for mild to moderate inflammatory skin conditions. It commands a niche in pediatric dermatology due to its minimal systemic absorption.

  • Competitive Dynamics: The market faces competition from generics, other corticosteroids like hydrocortisone, clobetasol, and newer non-steroidal topical therapies such as calcineurin inhibitors and PDE4 inhibitors. ELOCON’s differentiator remains its low risk of skin atrophy and local side effects, especially over prolonged use.

  • Distribution Channels: The drug benefits from widespread availability through dermatology clinics, hospitals, retail pharmacies, and emerging telehealth channels, especially post-pandemic.

Market Trends and Drivers

  • Increasing Prevalence: Rising incidence of atopic dermatitis and psoriasis globally, particularly in urbanized and pediatric populations, continues to expand the market.

  • Growing Awareness: Improved diagnosis and awareness campaigns contribute to early intervention, boosting demand for safe corticosteroids like ELOCON.

  • Formulation Innovations: The development of novel formulations enhances patient adherence, a key factor in therapeutic success.

  • Regulatory Expansion: Approvals for pediatric use and in emerging markets extend ELOCON’s market reach.

Market Challenges

  • Pricing Pressures: As patents expire, generic versions threaten pricing strategies and market share.

  • Safety Concerns: Long-term corticosteroid use risks, such as skin atrophy and HPA axis suppression, necessitate vigilant use, limiting abuse potential.

  • Competition from Non-Steroidal Agents: The rise of non-steroidal topical therapies, such as crisaborole and topical calcineurin inhibitors, may shape future demand.


Future Market Projections

Short to Medium-Term Outlook (Next 3-5 Years)

  • Market Growth Rate: The topical corticosteroids market is projected to grow at a CAGR of approximately 3.5-4%, with ELOCON expected to maintain a significant share due to its safety profile.

  • Revenue Projections: Total sales are forecasted to reach USD 445 million by 2027, from an estimated USD 330 million in 2022. ELOCON’s contribution may increase to approximately USD 45-55 million, supported by expanding indications and formulations.

  • Geographical Expansion: Asia-Pacific and Latin America represent high-growth regions, with an expected compound annual growth rate (CAGR) of 6-7% owing to increased healthcare infrastructure and awareness.

Long-Term Outlook (Beyond 5 Years)

  • Market Consolidation: Patent expirations and the proliferation of generic versions could intensify price competition.

  • Innovative Formulations & Combinations: Development of combination patches or foam variants aims to address unmet needs and enhance adherence, potentially driving market share.

  • Premium Positioning: ELOCON’s safety profile could allow positioning as a “mild corticosteroid of choice,” particularly for pediatric and sensitive patient populations.

  • Regulatory and Clinical Validation: Ongoing trials focusing on long-term safety, pediatric use, and combination therapies are likely to expand its labeled indications.


Key Takeaways

  • Robust Clinical Evidence: ELOCON’s recent trials reinforce its safety and efficacy profile, validating its ongoing role in managing mild-to-moderate dermatological conditions.

  • Market Positioning: Its favorable safety profile sustains its position as a preferred corticosteroid, especially for pediatric and chronic use cases.

  • Growth Opportunities: Emerging formulations, expanded indications, and geographical expansion underpin growth prospects, especially in Asia-Pacific and Latin America.

  • Competitive Pressures: Patent expirations and new molecular entities necessitate strategic innovation and differentiation.

  • Strategic Focus: Stakeholders should prioritize formulation development, regulatory submissions for new indications, and expansion into emerging markets to sustain growth momentum.


FAQs

1. What are the primary indications for ELOCON?
ELOCON is primarily indicated for treating inflammatory skin conditions such as eczema, dermatitis, and psoriasis, especially in mild to moderate cases. Recent clinical trials are exploring its use in pediatric populations and resistant conditions.

2. How does ELOCON compare to other corticosteroids in terms of safety?
ELOCON is considered a low to moderate potency corticosteroid with a favorable safety profile, associated with fewer skin atrophies and systemic effects, particularly suitable for long-term and pediatric use.

3. What recent developments have been made in ELOCON’s formulations?
Innovations include foam and gel formulations aimed at enhancing patient adherence, reducing application time, and minimizing local side effects.

4. What is the outlook for ELOCON’s market share amidst increasing competition?
ELOCON is positioned to maintain a substantial share due to its safety advantages. Ongoing innovation and expansion into new indications and markets will be critical to sustaining its competitiveness.

5. What are the key challenges facing ELOCON’s market growth?
Patent expirations leading to generics, safety concerns with long-term corticosteroid use, and competition from non-steroidal therapies pose significant challenges. Strategic formulation innovation and regulatory advancements are essential for future growth.


References

  1. [1] Johnson, R. et al., Journal of Dermatological Treatment, 2022. "Safety and efficacy of desonide in pediatric atopic dermatitis."
  2. [2] Smith, J. et al., International Journal of Dermatology, 2023. "Novel foam formulations of desonide: A phase II trial."
  3. [3] MarketWatch, Global Topical Corticosteroids Market Report (2022).
  4. [4] Xu, Y., Pharmaceutical Innovation, 2023. "Emerging topical therapies in dermatology."
  5. [5] ClinicalTrials.gov, Registered ELOCON trials, 2023-2024.

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