Biopharma Transcript

Sellas Life Sciences Group, Inc. SLS

Nasdaq · Phase 3 · hematology · protein/peptide · EDGAR · Updated Nov 4, 2026

Sellas Life Sciences Group, Inc. (Nasdaq: SLS) is a hematology drug developer. Its lead program, Galinpepimut-S (GPS), is in Phase 3 for Acute myeloid leukemia (AML) maintenance, second complete remission (CR2). Its next catalyst on record is SLS009: Topline data for SLS009 Phase 2 trial in newly diagnosed first-line AML expected in Q4 2026. (Q4 2026).

Upcoming catalysts

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

Next further out: SLS009 — Topline data for SLS009 Phase 2 trial in newly diagnosed first-line AML expected in Q4 2026. (Q4 2026). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
Galinpepimut-S (GPS)Acute myeloid leukemia (AML) maintenance, CR2protein/peptidePhase 3
SLS009 (tambiciclib)Newly diagnosed, first-line AML eligible for aza/ven therapysmall moleculePhase 2
SLS009 (tambiciclib)Relapsed/refractory AMLsmall moleculePhase 2

Recent results and decisions

  1. Aug 11, 2026
    n/a SELLAS obtained promising preclinical results for SLS009 in PDAC and intends to support clinical development at a top-tier academic institution.SLS009 has demonstrated the ability to act as a single agent in PDAC cells largely resistant to leading RAS inhibitors and synergize with the RAS inhibition mechanism of action. Filing
  2. Mar 19, 2026
    started First patient dosed in 80-patient Phase 2 trial of SLS009 with AZA/VEN in newly diagnosed/early-refractory AML.After receiving constructive feedback from the FDA, SELLAS dosed the first patient in an 80-patient trial in newly diagnosed AML patients as well as those who become refractory early to AZA/VEN treatment which we established through our extensive transcriptomics, genomics, and proteomics models. Filing
  3. Mar 19, 2026
    positive Phase 2 SLS009 + AZA/VEN in r/r AML-MR (ASH Dec 2025): ORR 46%, CR/CRi 29% among 35 evaluable patients; no DLTs.among the 35 evaluable patients, the overall response rate (CR/Cri/MLFS) was 46%, including 29% achieving CR/CRi. Filing

For subscribers

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