Biopharma Transcript

Adicet Bio, Inc. ACET

Nasdaq · Phase 1 · immunology/inflammation · cell therapy · EDGAR · Updated Oct 24, 2026

Adicet Bio, Inc. (Nasdaq: ACET) is an immunology/inflammation drug developer. Its lead program, prula-cel (prulacabtagene leucel, ADI-001), is in Phase 1 for autoimmune diseases (lupus nephritis, SLE, SSc, AAV, IIM, SPS). Its next catalyst on record is prula-cel: Potential pivotal program start in LN, subject to regulatory clearance (H2 2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: prula-cel — Potential pivotal program start in LN, subject to regulatory clearance (H2 2026). 15 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
prula-cel (CD20 CAR gamma delta T) - LN/SLE/SSc/AAV/IIM/SPSautoimmune diseasescell therapyPhase 1
prula-cel - rheumatoid arthritistreatment-refractory rheumatoid arthritiscell therapyPhase 1
ADI-212 (PSMA CAR gamma delta T)metastatic castration-resistant prostate cancercell therapyPre-clinical
In vivo CAR-T platform/pipelinehematologic malignancies and solid tumorscell therapyPre-clinical

Recent results and decisions

  1. Sep 28, 2026
    positive Phase 1 prula-cel in SLE/LN (22 evaluable): at 12 months 50% of LN patients had complete renal response and 54% achieved DORIS remission, no CRS above Grade 2, no ICANS or IEC-HS.At the 12-month mark, 50% of evaluable lupus nephritis patients achieved a complete renal response (CRR) and 54% of evaluable patients achieved DORIS remission. Filing
  2. Aug 28, 2026
    positive Prula-cel Phase 1 study showed 54% DORIS remission and 50% complete renal response at 12 months in SLE/LN patients with favorable safety profile.At the 12-month mark, 50% of evaluable lupus nephritis patients achieved a complete renal response (CRR) and 54% of evaluable patients achieved DORIS remission. Filing

For subscribers

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