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Trial · NCT05941845

Interferon Alfa Therapy Based on Th17 Profile in Membranous Nephropathy

NCT05941845, Phase 2, Terminated, Centre Hospitalier Universitaire de Nice

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Interferon Alfa Therapy Based on Th17 Profile in Membranous Nephropathy. Trials, record NCT05941845. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05941845

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Trial

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

Title
Interferon Alfa Therapy Based on Th17 Profile in Membranous Nephropathy
NCT number
NCT05941845
Status
Terminated
Phases
Phase 2
Enrollment
4 participants, actual
Lead sponsor
Centre Hospitalier Universitaire de Nice
Conditions
Membranous Nephropathy
Interventions
Peginterferon Alfa-2A 180 MCG/ML Injectable Solution
First posted
2023-07-12
Last updated
2026-06-18

Source ClinicalTrials.gov

Registered outcomes7

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

ListOutcomeTime frameDescription
PrimaryMembranous nephropathy immunological activity monitoring over 6-month interferon alfa treatment18 monthsIntra-individual variation in anti-PLA2R1 antibody titer (ELISA titer in RU/mL), before and after 6 months of treatment with IFN alfa
SecondaryNephrotic syndrome monitoring over 6-month interferon alfa treatmentBaseline to Week 24Intra-individual variation in proteinuria (g/g) under IFN alfa and stable symptomatic treatment
SecondaryNephrotic syndrome monitoring over 6-month interferon alfa treatmentBaseline to Week 24Intra-individual variation in albuminemia (g/L) under IFN alfa and stable symptomatic treatment
SecondaryImmune response monitoring over 6-month interferon alfa treatmentBaseline to Week 24Intra-individual variation in cytokine profile (assay of 8 cytokines in pg/ml: IL-12p70; IL-17A; IL-4; IL-5; IL-1β; IL-10; IFNα; IL-6) before and after 6 months of personalized treatment with IFN alfa
SecondaryImmune response monitoring over 6-month interferon alfa treatmentBaseline to Week 24Intra-individual variation in cytokine profile (assay of 1 cytokine in UI/ml: IFNγ) before and after 6 months of personalized treatment with IFN alfa
SecondaryClinical Tolerance monitoring over 6-month interferon alfa treatmentAt Week 52Percentage of Participants with clinical Adverse Events (AEs)
SecondaryBiological Tolerance monitoring over 6-month interferon alfa treatmentAt Week 52Percentage of Participants with biological Adverse Events (AEs)

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/NCT05941845

GET https://conductscience.org/api/trials/v1/NCT05941845/registered