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A Phase 1/2, Open-label, Safety and Dosing Study of Autologous CART Cells (Desmoglein 3 Chimeric Autoantibody Receptor T Cells [DSG3-CAART] or CD19-specific Chimeric Antigen Receptor T Cells [CABA-201]) in Subjects With Active, Pemphigus Vulgaris (RESET-PV)

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NCT04422912 · readout ≤ 896 d

Sponsored by Cabaletta Bio (industry) · CABA — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
40estimated
Sites
13
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2020-09-29actualWhen the study began enrolling
Primary completionJan 2029estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2029estimatedThe whole study's end, after follow-up
First posted2020-06-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Pemphigus Vulgaris

Interventions

  • Biological: DSG3-CAART
  • Biological: CABA-201

Primary outcomes

what the primary-completion date above is the date OF
Adverse events, including Dose Limit Toxicity
measured 3 months
For CABA-201 Sub-study: To evaluate adverse events reported by subjects
measured Up to 28 days after CABA-201 infusion

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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