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Trial · NCT03989206

Long-term Safety and Efficacy of Nemolizumab With Moderate-to-severe Atopic Dermatitis

NCT03989206, Phase 3, Completed, Galderma R&D

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Long-term Safety and Efficacy of Nemolizumab With Moderate-to-severe Atopic Dermatitis. Trials, record NCT03989206. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03989206

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Trial

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

Title
Long-term Safety and Efficacy of Nemolizumab With Moderate-to-severe Atopic Dermatitis
NCT number
NCT03989206
Status
Completed
Phases
Phase 3
Enrollment
1,935 participants, actual
Lead sponsor
Galderma R&D
Conditions
Moderate-to-Severe Atopic Dermatitis
Interventions
Nemolizumab
First posted
2019-06-18
Last updated
2026-10-20

Source ClinicalTrials.gov

Registered outcomes22

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

ListOutcomeTime frameDescription
PrimaryIncidence and Severity of TEAEsBaseline to Week 200
PrimaryIncidence of Serious TEAEsBaseline to Week 200
PrimaryIncidence and Severity of Adverse Events of Special Interest (AESIs) Throughout the StudyBaseline to Week 200
SecondaryProportion of Participants with IGA score = 0-1 at Each VisitBaseline to Week 200
SecondaryProportion of Participants with EASI-75 at Each VisitBaseline to Week 200
SecondaryChange and Percent Change From Baseline in Overall Eczema Area and Severity Index (EASI) Score at Each VisitBaseline to Week 200
EASI assesses severity and extent of AD signs through a composite score of erythema, induration/population, excoriation, and lichenification. The severity will be assessed on a scale of 0 (absent) to 3 (severe) for each of the 4 body areas: head/neck, trunk, upper limbs, and lower limbs, with half points allowed. The EASI score can range from 0 to 72 with higher scores representing greater severity of atopic dermatitis.
SecondaryProportion of Participants with IGA ≤ 2 at Each VisitBaseline to Week 200
SecondaryChange and Percent Change From Baseline in SCORAD Score at Each VisitBaseline to Week 200
SecondaryChange and Percent Change From Baseline in Participant-Reported Pruritus Using 10-cm VAS (SCORAD Sub-Component)Baseline to Week 200
SecondaryChange and Percent Change From Baseline in Participant-Reported Sleep Loss Using 10-cm VAS (SCORAD Sub-Component)Baseline to Week 200

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.

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
39068954DERIVEDPubMed
41081535DERIVEDPubMed

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/NCT03989206

GET https://conductscience.org/api/trials/v1/NCT03989206/registered?page=2