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An Open-label Phase I/II Safety and Feasibility Basket Study of UKT-CART19.1

NCT07932262, Phase 1, Phase 2, Not yet recruiting, University Hospital Tuebingen

Trial 10

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

FieldValueSource
TitleAn Open-label Phase I/II Safety and Feasibility Basket Study of UKT-CART19.1ClinicalTrials.gov
NCT numberNCT07932262ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesPhase 1, Phase 2ClinicalTrials.gov
Enrollment36 participants, estimatedClinicalTrials.gov
Lead sponsorUniversity Hospital TuebingenClinicalTrials.gov
ConditionsPemphigus Vulgaris (PV), ANCA Associated Vasculitis (AAV), Rheumatoid Arthritis (RA), IIM, Multiple Sclerosis, Immune Thrombocytopenic Purpura, Systemic Sclerosis (SSc)ClinicalTrials.gov
InterventionsCAR-T cells targeting CD19ClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 1

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

ListOutcomeTime frameDescriptionSource
PrimarySafety of UKT-CART19.1 in refractory and/or relapsed autoimmune diseases6 months
Safety of UKT-CART19.1 in refractory and/or relapsed autoimmune diseases at month 6 by * number of serious adverse events (SAE) * number of AE of special interests (AESI) in the first 28 days after CAR T cell infusion, classified according to CTCAE version 6.0 * non-relapse mortality (NRM) on day 28 and acute infusional toxicity after infusion of the IMP. AESI following the first 28 days after CAR T cell infusion are defined as described in chapter 7 and 9
ClinicalTrials.gov

Outcomes 0

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

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

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

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

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

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)