Biopharma Transcript

Cellectis S.A. CLLS

Nasdaq · Pre-clinical · cardio-renal-metabolic · gene therapy · EDGAR · Updated Oct 24, 2026

Cellectis S.A. (Nasdaq: CLLS) is a cardio-renal-metabolic drug developer. Its lead program, .HEAL-101, is in Pre-clinical for severe hypertriglyceridemia (in vivo APOC3 base editing). Its next catalyst on record is .HEAL-101: Preliminary Phase 1 IIT data (China) (H2 2027).

Upcoming catalysts

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

Next further out: .HEAL-101 — Preliminary Phase 1 IIT data (China) (H2 2027). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
.HEAL-101severe hypertriglyceridemia (APOC3 TALE base editor, LNP)gene therapyPre-clinical
.HEAL-201severe hypercholesterolemia (PCSK9 epigenetic editor, LNP)gene therapyPre-clinical

Recent results and decisions

  1. Aug 6, 2026
    positive BALLI-01 full Phase 1 at EHA 2026: target Phase 2 population ORR 100% (7/7), CR/CRi 57% (4/7), 75% MRD-negative; Gr>=3 CRS and ICANS each 4%.In the target Phase 2 population, an overall response rate (ORR) of 100% (7/7) was achieved with a complete remission/complete remission with incomplete count recovery (CR/CRi) rate of 57% (4/7), of whom 75% achieved minimal residual disease (MRD) negative status. Filing
  2. Aug 6, 2026
    positive NATHALI-01 translational data at EHA 2026: optimal dose cohort (n=8) ORR 88%, CR 63%.In the optimal dose cohort (n=8), ORR and complete response (CR) were 88% and 63%, respectively. Filing
  3. Aug 6, 2026
    positive ALPHA3 interim futility analysis (Allogene): MRD negativity 58.3% (7/12) with cema-cel vs 16.7% (2/12) with observation.showed that 58.3% (7/12) of patients in the cema-cel arm achieved MRD negativity compared to 16.7% (2/12) in the observation arm, representing a 41.6% absolute difference in MRD clearance between the arms Filing

2 more on record.

For subscribers

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