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Trial · NCT06531109

Characterization And Clinical Outcomes of AA Patients Treated With Ritlecitinib

NCT06531109, Active not recruiting, Pfizer

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Characterization And Clinical Outcomes of AA Patients Treated With Ritlecitinib. Trials, record NCT06531109. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06531109

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Trial

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

Title
Characterization And Clinical Outcomes of AA Patients Treated With Ritlecitinib
NCT number
NCT06531109
Status
Active not recruiting
Enrollment
450 participants, estimated
Lead sponsor
Pfizer
Conditions
Alopecia Areata
Interventions
Ritlecitinib
First posted
2024-07-31
Last updated
2026-11-06

Source ClinicalTrials.gov

Registered outcomes25

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

ListOutcomeTime frameDescription
PrimaryPercentage change from baseline in Severity of Alopecia Tool (SALT) score at week 2424 weeks from initiation of the treatmentSALT score is used to calculate the severity of alopecia areata. Physician calculate it by summing the percentage of hair loss in different regions of scalp.
SecondaryDemographic characteristic of participants: Age, sex, race, ethnicity, socio-economic status, area of residence, smoking statusBaseline
Number/percentage of patients by age, sex, race, ethnicity, socio-economic status, area of residence, smoking status. Race and ethnicity variables will only be collected in participating countries where it is allowed.
SecondaryDemographic Characteristic of Participants: Date of Initial AA diagnosisBaseline
SecondaryDemographic Characteristics of participants: Duration of AA since diagnosisBaseline
SecondaryDemographic characteristics of participants: Duration of current AA EpisodeBaseline
SecondaryDemographic Characteristic of Participants: Predominant AA phenotypeBaselinePredominant AA phenotype (eg, patchy; ophiasis; AT; AU, etc
SecondaryClinical Characteristics of participants: Severity of Alopecia Tool (SALT) ScoreBaselineSALT score is used to calculate the severity of alopecia areata.
SecondaryClinical characteristics of participants: Eyelash Assessment (ELA) scoreBaselineELA score is used to calculate the severity of the involvement of eyelashes.
SecondaryClinical Characteristics of participants: Eyebrow Assessment (EBA) ScoreBaselineEBA score is used to calculate the severity of the involvement of eyebrows
SecondaryClinical Characteristics of participants: number of affected nailsBaseline

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/NCT06531109

GET https://conductscience.org/api/trials/v1/NCT06531109/registered?page=2