Corporate presentation
Logotype for Karyopharm Therapeutics Inc

Karyopharm Therapeutics (KPTI) Corporate presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Karyopharm Therapeutics Inc

Corporate presentation summary

14 May, 2026

Strategic highlights and pipeline developments

  • 2026 marks a transformative year with major Phase 3 readouts and a strengthened shareholder foundation.

  • XPOVIO (selinexor) is approved in over 50 countries and targets multiple cancer indications, including myelofibrosis and endometrial cancer.

  • Topline Phase 3 SENTRY trial data in myelofibrosis reported in March 2026 showed an encouraging profile; additional Phase 3 data in endometrial cancer expected mid-2026.

  • U.S. myelofibrosis market opportunity is multi-billion dollar, with potential for selinexor plus ruxolitinib to reach ~$1B in annual net sales at peak.

  • Commercial organization is positioned for targeted launches, leveraging deep hematological oncology expertise.

Myelofibrosis clinical results and commercial opportunity

  • SENTRY Phase 3 trial: selinexor plus ruxolitinib achieved superior SVR35 rates (50% vs. 28%) at week 24, with rapid and sustained spleen volume reduction.

  • Similar symptom improvement to ruxolitinib alone; promising overall survival signal with >50% reduction in risk of death (HR 0.43, p=0.0222).

  • VAF reduction suggests potential disease modification; manageable safety profile consistent with known agents.

  • Significant unmet need: two-thirds of patients do not achieve SVR35 with current standard of care.

  • Commercial launch strategy targets both academic and community settings, covering 100% of key accounts.

Endometrial cancer program

  • Phase 3 XPORT-EC-042 trial focuses on TP53 wild-type endometrial cancer, a population with no approved targeted maintenance therapies.

  • SIENDO trial subgroup analysis showed median PFS benefit of 28.4 months for selinexor vs. 5.2 months for placebo in TP53 wild-type patients.

  • Safety profile in endometrial cancer consistent with known selinexor effects; most common adverse events include nausea, vomiting, and thrombocytopenia.

  • U.S. addressable market for TP53 wild-type endometrial cancer estimated at ~6,000+ patients annually.

  • Topline data from XPORT-EC-042 anticipated mid-2026.

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