Biopharma Transcript

Allogene Therapeutics, Inc. ALLO

Nasdaq · Phase 3 · oncology · cell therapy · EDGAR · Updated Nov 7, 2026

Allogene Therapeutics, Inc. (Nasdaq: ALLO) is an oncology drug developer. Its lead program, cema-cel (cemacabtagene ansegedleucel, previously ALLO-501A), is in Phase 3 for first-line consolidation treatment for patients newly diagnosed with large B-cell lymphoma (LBCL) with minimal residual disease (MRD) following 1L chemoimmunotherapy. Its next catalyst on record is ALLO-329 (RESOLUTION): clinical and translational data presentation at ACR Convergence (November 9, 2026).

Upcoming catalysts

  1. November 9, 2026
    ALLO-329 (RESOLUTION) — clinical and translational data presentation at ACR ConvergenceWe will present updated clinical and translational data from RESOLUTION at the 2026 American College of Rheumatology (ACR) Convergence on November 9, 2026.

Next further out: cema-cel (ALPHA3) — next clinical update (H1 2027). 3 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
cema-cel (ALPHA3 trial)first-line consolidation LBCL with MRDcell therapyPhase 3
ALLO-316advanced or metastatic clear cell renal cell carcinoma (RCC)cell therapyPhase 1
ALLO-329 (RESOLUTION trial)autoimmune diseases (SLE, IIM, SSc)cell therapyPhase 1
BCMA CAR (with or without CD70 Dagger)oncology (BCMA+ cancers, likely multiple myeloma)cell therapyPre-clinical
DLL3 CAR (with or without CD70 Dagger)small cell lung cancer and other neuroendocrine tumorscell therapyPre-clinical

Recent results and decisions

  1. Apr 13, 2026
    positive Interim futility analysis (24 pts): MRD negativity 58.3% (7/12) with cema-cel vs 16.7% (2/12) observation; no CRS, ICANS or GvHD; primary EFS endpoint remains blinded.At the protocol-defined data cutoff date, 58.3% (7/12) of patients in the cema-cel arm achieved MRD negativity compared to 16.7% (2/12) in the observation arm. Filing

For subscribers

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