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A Study of CNTY-101 in Participants With Refractory B Cell-mediated Autoimmune Diseases

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NCT06255028 · readout ≤ 742 d

Sponsored by Century Therapeutics, Inc. (industry) · IPSC — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
6actual
Sites
6
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
Start2025-02-06actualWhen the study began enrolling
Primary completionAug 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2028estimatedThe whole study's end, after follow-up
First posted2024-02-12actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-08actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Systemic Lupus Erythematosus
  • Lupus Nephritis
  • Idiopathic Inflammatory Myopathies
  • Diffuse Cutaneous Systemic Sclerosis

Interventions

  • Biological: CNTY-101
  • Biological: IL-2
  • Drug: Lymphodepleting Chemotherapy

Primary outcomes

what the primary-completion date above is the date OF
Percentage of Participants With Treatment-emergent Adverse Events (TEAEs) and Severity of TEAEs
measured Up to 29 days
Percentage of Participants With Dose Limiting Toxicities (DLTs)
measured Up to 28 days after first CNTY-101 infusion
Recommended Phase 2 Regimen (RP2R) of CNTY-101 With/Without IL-2 (With or Without Optimized LDC)
measured Up to 3 months after the first CNTY-101 infusion

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