MedPath

LEO LABORATORIES LIMITED

🇮🇪Ireland
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

220

Active:4
Completed:196

Trial Phases

6 Phases

Early Phase 1:1
Phase 1:74
Phase 2:52
+3 more phases

Drug Approvals

2

NMPA:2

Drug Approvals

Fusidic Acid Cream

Product Name
立思丁
Approval Number
H20130928
Approval Date
Dec 21, 2018
NMPA

Sodium Fusidate Ointment

Product Name
立思丁
Approval Number
H20150160
Approval Date
Mar 27, 2015
NMPA

Clinical Trials

Distribution across different clinical trial phases (193 trials with phase data)• Click on a phase to view related trials

Phase 1
74 (38.3%)
Phase 2
52 (26.9%)
Phase 3
50 (25.9%)
Phase 4
14 (7.3%)
Not Applicable
2 (1.0%)
Early Phase 1
1 (0.5%)

A 16-week Trial to Investigate the Efficacy and Safety of Delgocitinib Cream 20 mg/g in Adult Participants With Mild to Severe Palmoplantar Pustulosis

Phase 2
Not yet recruiting
Conditions
Palmoplantar Pustulosis
Interventions
Drug: Vehicle cream
First Posted Date
2025-06-10
Last Posted Date
2025-06-29
Lead Sponsor
LEO Pharma
Target Recruit Count
135
Registration Number
NCT07013201
Locations
🇺🇸

LEO Pharma Investigation Site, Mayfield Heights, Ohio, United States

🇺🇸

LEO Pharma Investigational Site, Philadelphia, Pennsylvania, United States

A Study to Evaluate Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of a Single Dose of LEO 158968

Phase 1
Recruiting
Conditions
Gout Flares
Joint Pain
Joint Inflammation
Interventions
First Posted Date
2024-06-06
Last Posted Date
2025-06-18
Lead Sponsor
LEO Pharma
Target Recruit Count
15
Registration Number
NCT06444867
Locations
🇬🇧

LEO Pharma Investigational Site, London, United Kingdom

A phase 3 multi-center trial to evaluate the efficacy and safety of tralokinumab in combination with topical corticosteroids in children (age 2 to <12 years) and infants (age 6 months to <2 years) with moderate-to-severe atopic dermatitis. The trial is randomized, double blind, placebo-controlled, and parallel-group for children (age 2 to <12 years) and open-label and single-group for infants (age 6 months to <2 years).

Phase 2/3
Recruiting
Conditions
Treatment of moderate-to-severe Atopic dermatitis
First Posted Date
2024-10-07
Last Posted Date
2025-03-31
Lead Sponsor
Leo Pharma A/S
Target Recruit Count
112
Registration Number
2023-503630-44-00
Locations
🇨🇿

Kozni ambulance Kutna Hora s.r.o., Hlouska, Czechia

🇨🇿

Nemocnice AGEL Novy Jicin a.s., Novy Jicin, Czechia

🇩🇰

Region Hovedstaden, Copenhagen Nv, Denmark

and more 45 locations

A Trial to Evaluate Efficacy, Safety, and Pharmacokinetics of Delgocitinib Cream in Chinese Adults and Adolescents With Moderate to Severe Chronic Hand Eczema

Phase 3
Active, not recruiting
Conditions
Chronic Hand Eczema
Interventions
Other: Vehicle cream
First Posted Date
2023-08-22
Last Posted Date
2025-02-24
Lead Sponsor
LEO Pharma
Target Recruit Count
360
Registration Number
NCT06004050
Locations
🇨🇳

LEO Pharma Investigational Site, Zhenjiang, China

A 32-week Trial to Evaluate the Efficacy and Safety of Tralokinumab in Subjects With Moderate-to-severe Atopic Hand Eczema Who Are Candidates for Systemic Therapy

Phase 3
Recruiting
Conditions
Atopic Dermatitis
Atopic Hand Eczema
Interventions
Drug: Placebo
First Posted Date
2023-07-24
Last Posted Date
2025-02-24
Lead Sponsor
LEO Pharma
Target Recruit Count
402
Registration Number
NCT05958407
Locations
🇬🇧

LEO Pharma Investigational Site, London, United Kingdom

🇪🇸

LEO Investigational Site, Badalona, Barcelona, Spain

🇪🇸

LEO Pharma Investigational site, Granada, Spain

and more 1 locations
  • Prev
  • 1
  • 2
  • 3
  • 4
  • 5
  • 44
  • Next

News

LEO Pharma's Tralokinumab Meets All Endpoints in Phase 3b Hand Atopic Dermatitis Trial

LEO Pharma announced positive 16-week interim results from the phase 3b ADHAND trial, with tralokinumab meeting all primary and secondary endpoints for moderate to severe atopic dermatitis on the hands.

uniQure Appoints Kylie O'Keefe as Chief Customer and Strategy Officer to Lead AMT-130 Commercialization for Huntington's Disease

uniQure has appointed Kylie O'Keefe as Chief Customer and Strategy Officer to lead the global commercialization strategy for AMT-130, the company's investigational gene therapy for Huntington's disease.

LEO Pharma Launches Phase 2a Trial of Delgocitinib Cream for Rare Skin Disease Palmoplantar Pustulosis

LEO Pharma has initiated the DELTA NEXT phase 2a trial to evaluate delgocitinib cream versus placebo in adults with mild to severe palmoplantar pustulosis, a rare inflammatory skin condition.

Robust Pipeline of 50+ Therapies Reshaping Moderate to Severe Atopic Dermatitis Treatment Landscape

• The moderate to severe atopic dermatitis market is experiencing significant growth with 45+ companies developing over 50 pipeline therapies, driven by rising global prevalence and increased awareness of the condition. • Recent advancements include promising biologics like rezpegaldesleukin (granted FDA fast-track designation), JAK inhibitors such as VC005 and QY201, and novel mechanisms targeting IL-4/IL-13 pathways, offering new hope for patients with inadequate response to current treatments. • Key players including Nektar Therapeutics, Corvus Pharmaceuticals, and Apogee Therapeutics are advancing clinical trials with significant milestones expected in late 2025, potentially transforming the therapeutic landscape for this chronic inflammatory skin condition.

LEO Pharma's Temtokibart Shows Promising Results in Phase 2b Trial for Moderate-to-Severe Atopic Dermatitis

LEO Pharma's investigational IL-22RA1 antagonist temtokibart achieved positive results for the primary endpoint at the three highest doses in a Phase 2b trial for moderate-to-severe atopic dermatitis.

LEO Pharma's Delgocitinib Cream Outperforms Alitretinoin in Landmark DELTA FORCE Trial for Chronic Hand Eczema

The phase 3 DELTA FORCE trial demonstrated superior efficacy of topical delgocitinib cream over oral alitretinoin capsules for severe chronic hand eczema, with results published in The Lancet.

Sanofi's Amlitelimab Shows Promising Results in Atopic Dermatitis Trial Following $1.45bn Kymab Acquisition

• Sanofi's amlitelimab (formerly KY1005), acquired through its $1.45 billion Kymab purchase, demonstrated significant efficacy in a Phase 2a trial for moderate to severe atopic dermatitis with an 80% improvement in EASI scores at the low dose. • The OX40 ligand-targeting antibody showed durable effects, with two-thirds of patients maintaining clear or almost clear skin 24 weeks after the final dose, positioning it as a potential complement to Sanofi's blockbuster Dupixent. • Despite increasing competition in the atopic dermatitis market from biologics and JAK inhibitors, Sanofi is advancing amlitelimab to Phase 2b trials, emphasizing the need for diverse treatment options for this challenging condition.

Delgocitinib Cream Shows "Super-Response" in Nearly Half of Chronic Hand Eczema Patients

Nearly 50% of patients with moderate to severe chronic hand eczema achieved a "deep response" with delgocitinib cream 20 mg/g by week 16, demonstrating significant relief from disease burden.

Survey Reveals Critical Gaps in Chronic Hand Eczema Understanding and Treatment Options

A new LEO Pharma survey finds 65% of dermatology providers acknowledge significant knowledge gaps in distinguishing chronic hand eczema (CHE) from atopic dermatitis, highlighting a critical need for education.

Phase 3 Trial Shows Delgocitinib Cream Effective for Adolescent Chronic Hand Eczema

LEO Pharma's delgocitinib 20 mg/g cream demonstrated significant efficacy in Phase 3 DELTA TEEN study for adolescents aged 12-17 with chronic hand eczema.

© Copyright 2025. All Rights Reserved by MedPath