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Study Evaluating SC291 in Subjects With Severe r/r B-cell Mediated Autoimmune Diseases (GLEAM)

← catalyst calendar

NCT06294236 · readout ≤ 499 d

Sponsored by Sana Biotechnology (industry) · SANA — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
7estimated
Sites
5
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
Start2024-04-29actualWhen the study began enrolling
Primary completionDec 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionMar 2028estimatedThe whole study's end, after follow-up
First posted2024-03-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Lupus Erythematosus
  • Systemic Lupus Erythematosus
  • SLE (Systemic Lupus)
  • Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
  • Granulomatous Polyangiitis
  • Microscopic Polyangiitis

Intervention

  • Biological: SC291 — also filed as Cyclophosphamide, Fludarabine

Primary outcome

what the primary-completion date above is the date OF
Evaluate safety and tolerability of SC291
measured 24 months

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