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Trial · NCT06004050

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

NCT06004050, Phase 3, Completed, LEO Pharma

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Trial to Evaluate Efficacy, Safety, and Pharmacokinetics of Delgocitinib Cream in Chinese Adults and Adolescents With Moderate to Severe Chronic Hand Eczema. Trials, record NCT06004050. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06004050

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Trial to Evaluate Efficacy, Safety, and Pharmacokinetics of Delgocitinib Cream in Chinese Adults and Adolescents With Moderate to Severe Chronic Hand Eczema
NCT number
NCT06004050
Status
Completed
Phases
Phase 3
Enrollment
362 participants, actual
Lead sponsor
LEO Pharma
Conditions
Chronic Hand Eczema
Interventions
Delgocitinib, Vehicle cream
First posted
2023-08-22
Last updated
2025-09-25

Source ClinicalTrials.gov

Registered outcomes19

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryInvestigator Global Assessment for Chronic Hand Eczema Score (IGA-CHE TS) at Week 16Week 16The IGA-CHE score ranges from 0 (clear) to 4 (severe). Treatment response is defined as a score of 0 or 1.
SecondaryHand Eczema Severity Index (HECSI)-90 at Week 16Week 16Defined as at least a 90% improvement in HECSI score from baseline.
SecondaryHECSI-75 at Week 16Week 16Defined as at least a 75% improvement in HECSI score from baseline.
SecondaryPercentage Change in HECSI Score From Baseline to Week 16Baseline and Week 16HECSI score is used to rate the severity of hand eczema and ranges from 0 (lowest possible score) to 360 (highest possible score).
SecondaryNumber of Participants With Reduction of Hand Eczema Symptom Diary (HESD) Itch Score by ≥4 Points From Baseline at Week 16Baseline and Week 16
SecondaryNumber of Participants With Reduction of HESD Score by ≥4 Points From Baseline at Week 16Baseline and Week 16
SecondaryNumber of Participants With Reduction of HESD Pain Score by ≥4 Points From Baseline at Week 16Baseline and Week 16
SecondaryChange in Dermatology Life Quality Index (DLQI) Score From Baseline to Week 16Baseline and Week 16
SecondaryChange in HESD Score From Baseline to Week 16Baseline and Week 16
SecondaryChange in HESD Itch Score From Baseline to Week 16Baseline and Week 16

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT06004050

GET https://conductscience.org/api/trials/v1/NCT06004050/registered