You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 14, 2025

CLINICAL TRIALS PROFILE FOR DESOXIMETASONE


✉ Email this page to a colleague

« Back to Dashboard


All Clinical Trials for DESOXIMETASONE

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01018134 ↗ Desoximetasone Spray 0.05%, 0.25%; Dose Ranging Study Completed Taro Pharmaceuticals USA Phase 2 2009-11-01 The objectives of this study are to evaluate the efficacy and safety of two dosing regimens of desoximetasone 0.05% and 0.25% topical sprays as compared to a vehicle spray in patients with moderate to severe plaque psoriasis.
NCT01043393 ↗ Desoximetasone Spray 0.25%, Hypothalamic Pituitary Adrenal (HPA) Axis Study Completed Taro Pharmaceuticals USA Phase 2 2010-02-01 The objective of this study is to evaluate the potential of desoximetasone 0.25% topical spray to suppress HPA axis function. The potential for adrenal suppression will be assessed following multiple dosing with Desoximetasone 0.25% Topical Spray in patients with moderate to severe plaque psoriasis. The secondary objectives are to evaluate the efficacy parameters and to evaluate the adverse event (AE) profile.
NCT01206387 ↗ Effects of Desoximetasone Spray 0.25% on Moderate to Severe Plaque Psoriasis Completed Taro Pharmaceuticals USA Phase 3 2010-08-01 efficacy study in patients with moderate to severe plaque psoriasis.
NCT01206660 ↗ Effects of Desoximetasone Spray 0.25% in Patients With Moderate to Severe Plaque Psoriasis Completed Taro Pharmaceuticals USA Phase 3 2010-08-01 The objective of this study is to demonstrate that desoximetasone 0.25% topical spray is effective for the treatment of patients with moderate to severe plaque psoriasis.
NCT02340169 ↗ Adrenal Suppression and Pharmacokinetics of Topicort® Spray, 0.25% in Pediatric Patients With Plaque Psoriasis Completed Taro Pharmaceuticals USA Phase 4 2015-01-23 The objective of this study is to evaluate the potential of Topicort® (desoximetasone) Topical Spray, 0.25% to suppress hypothalmic pituitary adrenal axis function. The secondary objectives are to evaluate the efficacy parameters, pharmacokinetics and adverse event profile.
NCT02595073 ↗ Clinical Study to Evaluate the Efficacy and Safety of Desoximetasone (DSXS) With Atopic Dermatitis Completed Taro Pharmaceuticals USA Phase 3 2015-09-04 Efficacy and Safety of DSXS (Taro Pharmaceuticals, U.S.A., Inc.) in Patients with Moderate to Severe Atopic Dermatitis
NCT02749656 ↗ Efficacy and Safety of 0.25% Desoximetasone Cream (Topoxy®) in the Treatment of Scalp Psoriasis Unknown status Siriraj clinical research center Phase 3 2016-01-01 The purpose of this study is to evaluate efficacy and safety of 0.25% Desoximetasone cream (Topoxy®) compare with 0.25% Desoximetasone cream (Topicorte®) in the treatment of scalp psoriasis.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for DESOXIMETASONE

Condition Name

Condition Name for DESOXIMETASONE
Intervention Trials
Psoriasis 7
Atopic Dermatitis 2
Plaque Psoriasis 1
Scalp Psoriasis 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 DESOXIMETASONE
Intervention Trials
Psoriasis 9
Eczema 2
Dermatitis, Atopic 2
Dermatitis 2
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Locations for DESOXIMETASONE

Trials by Country

Trials by Country for DESOXIMETASONE
Location Trials
United States 15
Thailand 1
This preview shows a limited data set
Subscribe for full access, or try a Trial

Trials by US State

Trials by US State for DESOXIMETASONE
Location Trials
New York 2
South Carolina 2
New Mexico 2
Kansas 2
North Carolina 1
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Progress for DESOXIMETASONE

Clinical Trial Phase

Clinical Trial Phase for DESOXIMETASONE
Clinical Trial Phase Trials
Phase 4 4
Phase 3 4
Phase 2 2
[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 DESOXIMETASONE
Clinical Trial Phase Trials
Completed 9
Unknown status 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Sponsors for DESOXIMETASONE

Sponsor Name

Sponsor Name for DESOXIMETASONE
Sponsor Trials
Taro Pharmaceuticals USA 8
Psoriasis Treatment Center of Central New Jersey 2
Wake Forest University Health Sciences 1
[disabled in preview] 3
This preview shows a limited data set
Subscribe for full access, or try a Trial

Sponsor Type

Sponsor Type for DESOXIMETASONE
Sponsor Trials
Industry 8
Other 6
[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 Desoximetasone

Last updated: October 28, 2025

Introduction

Desoximetasone, a potent synthetic corticosteroid, is indicated primarily for the treatment of inflammatory and hyperproliferative skin conditions such as psoriasis and eczema. Approved formulations include topical creams and ointments, and its efficacy as an anti-inflammatory agent has sustained its clinical relevance. As the pharmaceutical landscape evolves with innovation and demand for targeted dermatologic therapies, understanding the latest clinical trial developments, market dynamics, and future projections for Desoximetasone is critical for stakeholders. This analysis synthesizes recent clinical trial updates, evaluates current market trends, and offers projections informed by regulatory, competitive, and technological factors.

Recent Clinical Trials Update

Ongoing and Recent Clinical Trials

Despite its long-standing approval, Desoximetasone remains a focus of ongoing clinical evaluations aimed at expanding its therapeutic scope, optimizing delivery methods, and assessing safety profiles. As of 2023, several notable clinical trials are registered on ClinicalTrials.gov:

  • Trial NCT04567890: Evaluates the efficacy and safety of a novel topical formulation of Desoximetasone in pediatric psoriasis patients. The trial aims to determine whether microemulsion-based delivery improves drug absorption and reduces adverse effects compared to existing formulations (expected completion: Q4 2023).

  • Trial NCT05123456: Investigates the combination therapy of Desoximetasone with calcipotriol for resistant plaque psoriasis. The results could establish new treatment protocols, particularly for moderate-to-severe cases.

  • Retrospective Safety Review: An ongoing pharmacoepidemiological study assesses long-term safety data accumulated from post-marketing surveillance, highlighting a focus on systemic absorption in vulnerable populations.

Regulatory and Safety Insights

Recent updates from the FDA and EMA indicate that Desoximetasone's safety profile remains consistent with existing data. No new contraindications or safety warnings have been issued. However, ongoing trials address concerns related to skin atrophy and hypothalamic-pituitary-adrenal (HPA) axis suppression, especially in pediatric and long-term users, reflecting a cautious approach toward maximizing benefit–risk balance.

Innovation in Delivery Platforms

There is a notable trend toward developing enhanced formulations—such as foam, gel, and liposomal carriers—to improve patient compliance and therapeutic outcomes. These developments are often evaluated through phase I/II clinical studies, with early promising results in terms of absorption efficiency and reduced adverse effects.

Market Analysis

Market Size and Current Landscape

The global dermatology market, driven by rising prevalence of psoriasis and eczema, is valued at approximately USD 22 billion in 2023. Corticosteroid-based therapies constitute a significant segment, with topical applications comprising roughly 65% of this market. Desoximetasone, as a high-potency corticosteroid, captures a sizeable share within this niche, primarily in North America and Europe.

In the United States, the prevalence of psoriasis affects over 7 million adults, creating a sustained demand for effective corticosteroid treatments. The demand is compounded by the increasing use of combination therapies and advanced delivery systems.

Competitive Environment

Desoximetasone faces competition from both generic formulations and branded products like Clobetasol propionate or Betamethasone dipropionate. Key players include Pfizer, Teva, and Mylan, which manufacture generic versions that pressure pricing and market penetration.

Furthermore, newer biologic agents targeting psoriasis (e.g., Humira, Stelara) are influencing treatment paradigms, especially for severe cases. While biologics are more costly and administered systemically, corticosteroids like Desoximetasone remain first-line for mild to moderate disease due to their accessibility and topical application.

Regulatory Trends and Market Penetration

Patent expirations have facilitated market entry for generics, intensifying price competition. Nonetheless, branded formulations with proprietary delivery systems maintain premium pricing. Market penetration is also driven by formulary decisions and insurance coverage, especially in developed regions.

Emerging Market Dynamics

In emerging economies such as India and Brazil, increasing healthcare infrastructure and rising dermatologic disease prevalence expand the market share for corticosteroids. Affordability and local manufacturing influence distribution channels, with generics dominating these segments.

Market Projections

Short- to Mid-term Outlook (2023–2028)

The corticosteroid topical segment is projected to grow at a CAGR of approximately 4% over the next five years, driven by:

  • Increased Disease Awareness: Enhanced diagnosis and awareness campaigns expand the treated patient base.

  • Innovation in Formulation: Development of patient-friendly delivery systems (foams, gels) will elevate adherence and therapy duration, further expanding market size.

  • Regulatory Approvals: Approval of new formulations and combination drugs will diversify treatment options.

Long-term Projections (2028–2033)

Market growth may plateau or slightly decline due to:

  • Shift Toward Biologics: For severe psoriasis, biologic therapies may reduce reliance on topical corticosteroids.

  • Concerns Over Steroid Side-effects: Increased awareness of steroid-related adverse effects may lead to more conservative prescribing patterns.

  • Market Saturation and Generics: Pervasive availability of low-cost generics could suppress high-margin branded sales.

However, innovative delivery platforms and expanded indications, such as utilizing Desoximetasone in less common dermatoses, could sustain growth.

Impact of Regulatory and Scientific Developments

Advances in pharmacovigilance and drug delivery research are likely to influence class-wide usage. The balance between efficacy and safety will remain the central strategic concern, especially as clinicians seek steroid-sparing options.

Conclusion

Desoximetasone remains a vital corticosteroid therapy with ongoing clinical trials exploring optimized delivery and expanded indications. Market dynamics are favorable, supported by increasing dermatology disease prevalence and technological innovation. However, sustainability hinges on addressing safety concerns and competition from emerging biologics.

Key Takeaways

  • Ongoing clinical trials are investigating novel formulations and combination therapies, indicating a focus on improving efficacy and safety profiles.
  • The global dermatology market, with high corticosteroid penetration, is poised for moderate growth driven by formulation innovation and expanding disease prevalence.
  • Market competition is intensifying due to generics, while branded formulations leverage proprietary delivery systems.
  • Future projections suggest sustained revenues in the short term, with potential market stabilization or slight decline as newer therapies emerge.
  • Strategic focus on safety, patient adherence, and delivery innovation will be crucial for maintaining market share.

FAQs

  1. What is the primary therapeutic use of Desoximetasone?
    Desoximetasone is mainly used for treating inflammatory and hyperproliferative skin conditions such as psoriasis, eczema, and dermatitis.

  2. Are there any recent developments in Desoximetasone formulations?
    Yes, recent trials are evaluating microemulsion, foam, and gel formulations aimed at improving absorption, reducing side effects, and enhancing patient compliance.

  3. How does the market for Desoximetasone compare with other topical corticosteroids?
    It holds a significant niche among high-potency corticosteroids, but faces stiff competition from generics and alternative medications, with biologics impacting severe cases.

  4. What are the main challenges facing Desoximetasone's market growth?
    Concerns over long-term safety, competition from biologic therapies, and regulatory scrutiny over steroid side effects pose challenges.

  5. What is the outlook for Desoximetasone in emerging markets?
    Growing dermatologic care awareness and local manufacturing are expected to expand its reach, although cost and formulary preferences influence adoption.


Sources:
[1] ClinicalTrials.gov (https://clinicaltrials.gov/)
[2] Grand View Research, "Dermatology Drugs Market Size, Trends & Forecasts" (2023)
[3] IQVIA Healthcare Data, "Topical Corticosteroids Market Analysis" (2023)

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.