Karyopharm Therapeutics

Karyopharm Therapeutics

KPTI
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KPTI · Stock Price

USD 8.85+1.22 (+15.99%)
Market Cap: $202.6M

Historical price data

Overview

Karyopharm Therapeutics is an innovation-driven, commercial-stage company focused on discovering and developing novel oral cancer therapies targeting nuclear export. Its foundational achievement is the FDA approval of selinexor (XPOVIO®) for relapsed/refractory multiple myeloma and diffuse large B-cell lymphoma (DLBCL). The company's strategy leverages its proprietary oral SINE technology platform to expand selinexor into earlier treatment lines and new indications, while developing next-generation compounds like eltanexor and verdinexor to improve tolerability and efficacy. Karyopharm aims to establish XPO1 inhibition as a cornerstone of cancer treatment across a spectrum of malignancies.

OncologyHematologic MalignanciesSolid Tumors

Technology Platform

Oral Selective Inhibitor of Nuclear Export (SINE) platform targeting the nuclear export protein XPO1, a fundamental mechanism in oncogenesis that forces nuclear retention of tumor suppressor proteins and induces cancer cell apoptosis.

Pipeline

87
87 drugs in pipeline7 in Phase 3

Funding History

5
Total raised:$439M
PIPE$150M
IPO$120M
Series C$101M
Series B$48M

Opportunities

Near-term value inflection from the Phase 3 SENTRY trial in myelofibrosis, which met its first primary endpoint, could open a significant new market.
Expanding selinexor into earlier lines of myeloma therapy and into large indications like AML/MDS, coupled with the development of better-tolerated next-generation SINE compounds, offers multiple pathways for growth.

Risk Factors

High clinical development risk with pivotal readouts, intense competition in core oncology markets, financial vulnerability requiring additional capital leading to potential dilution, and a pipeline heavily concentrated on the SINE mechanism which faces regulatory and safety scrutiny.

Competitive Landscape

Karyopharm faces intense competition from novel modalities (bispecifics, CAR-T) in myeloma and lymphoma, and from JAK inhibitors in myelofibrosis. Its key advantage is first-mover status with a novel, oral XPO1 inhibitor mechanism, but it must continuously demonstrate differentiated efficacy and tolerability against evolving standards of care.