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Trial · NCT03663855

Effect of Increasing Doses of Tiopronin on Cystine Capacity in Patients With Cystinuria

NCT03663855, Phase 2, Completed, NYU Langone Health; results first posted 2021-12-17

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effect of Increasing Doses of Tiopronin on Cystine Capacity in Patients With Cystinuria. Trials, record NCT03663855. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03663855

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Trial

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

Title
Effect of Increasing Doses of Tiopronin on Cystine Capacity in Patients With Cystinuria
NCT number
NCT03663855
Status
Completed
Phases
Phase 2
Enrollment
10 participants, actual
Lead sponsor
NYU Langone Health
Conditions
Cystinuria
Interventions
Tiopronin
First posted
2018-09-10
Last updated
2021-12-17
Results first posted
2021-12-17

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryChange in Cystine Capacity From BaselineBaseline; Day 7This measure reflects the ability of urine to take up more cystine

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Cystine Capacity From BaselineBaseline; Day 7mg/LMEAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Change in Cystine Capacity From BaselineCystinuria PatientsPhase 1-63.6Standard Deviation 24.8mg/L
Change in Cystine Capacity From BaselineCystinuria PatientsPhase 276Standard Deviation 18.1mg/L
Change in Cystine Capacity From BaselineCystinuria PatientsPhase 353.4Standard Deviation 17.7mg/L
Change in Cystine Capacity From BaselineCystinuria PatientsPhase 4103.1Standard Deviation 27.4mg/L

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCystinuria Patients10
Overall StudyCOMPLETEDCystinuria Patients10
Overall StudyNOT COMPLETEDCystinuria Patients0

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 totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCystinuria Patients010
Total, other adverse eventsCystinuria Patients010
Total, serious adverse eventsCystinuria Patients010

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/NCT03663855

GET https://conductscience.org/api/trials/v1/NCT03663855/registered