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Trial · NCT02061137

Study to Assess Safety and Efficacy of Fingolimod in Children With Rett Syndrome

NCT02061137, Phase 1, Phase 2, Completed, University Hospital, Basel, Switzerland

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study to Assess Safety and Efficacy of Fingolimod in Children With Rett Syndrome. Trials, record NCT02061137. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02061137

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Trial

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

Title
Study to Assess Safety and Efficacy of Fingolimod in Children With Rett Syndrome
NCT number
NCT02061137
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
6 participants, actual
Lead sponsor
University Hospital, Basel, Switzerland
Conditions
Rett's Syndrome
Interventions
fingolimod (FTY720)
First posted
2014-02-12
Last updated
2018-06-15

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryLevels of Brain derived neurotrophic factor (BDNF) in blood and cerebrospinal fluid before and under treatmentchange of BDNF measured at Baseline, at first dose, at 6 and at 12 months after start of treatment.

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.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
33407685DERIVED

Source PubMed

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/NCT02061137

GET https://conductscience.org/api/trials/v1/NCT02061137/registered