Biopharma Transcript

Alumis Inc. ALMS

Nasdaq · Phase 3 · immunology/inflammation · small molecule · EDGAR · Updated Nov 4, 2026

Alumis Inc. (Nasdaq: ALMS) is an immunology/inflammation drug developer. Its lead program, envudeucitinib (envu, formerly ESK-001), is in Phase 3 for moderate-to-severe plaque psoriasis. Its next catalyst on record is A-005: Initiate Phase 2 biomarker trial in Parkinson's disease (H1 2027).

Upcoming catalysts

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

Next further out: A-005 — Initiate Phase 2 biomarker trial in Parkinson's disease (H1 2027). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
envudeucitinib (envu)plaque psoriasis (pivotal Phase 3 ONWARD1/ONWARD2 complete; ONWARD3 LTE ongoing)small moleculePhase 3
envudeucitinib (envu)systemic lupus erythematosussmall moleculePhase 2
A-005CNS / neuroinflammatory disease (Parkinson's disease biomarker trial planned)small moleculePhase 1
lonigutamabthyroid eye diseaseantibodyPhase 1

Recent results and decisions

  1. Sep 1, 2026
    missed Phase 2b LUMUS did not meet its primary (BICLA Week 48) or secondary endpoints in the overall population (n=408); responses seen in prespecified IFNGS-high subgroup.LUMUS trial did not meet its primary and secondary endpoints in the overall trial population Filing
  2. Aug 10, 2026
    positive ONWARD3 long-term extension: after up to 48 weeks of continuous treatment 75% reached PASI 90 and 54% PASI 100 (n=773), with no new safety signals.75% and 54% of patients achieved PASI 90 and PASI 100, respectively Filing
  3. Jan 6, 2026
    met Phase 3 ONWARD1 met co-primary endpoints PASI 75 and sPGA 0/1 at Week 16 vs placebo (p<0.0001); pooled avg 74% PASI 75, 59% sPGA 0/1; ~65% PASI 90 and >40% PASI 100 at Week 24.Envudeucitinib met all primary and secondary endpoints with high statistical significance in ONWARD1 and ONWARD2. Filing

For subscribers

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