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Karyopharm Therapeutics Inc. (Nasdaq: KPTI) is a commercial-stage pharmaceutical company focused on pioneering novel cancer therapies. The company specializes in the discovery, development, and commercialization of drugs targeting nuclear export proteins for the treatment of cancer and other significant diseases. Its flagship product, XPOVIO® (selinexor), is a first-in-class, oral exportin 1 (XPO1) inhibitor and is approved in the U.S. for multiple oncology indications. These include combination therapies with Velcade® (bortezomib) and dexamethasone for multiple myeloma, as well as treatments for adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL).
Recent achievements highlight the company's commitment to advancing its late-stage clinical pipeline. Notably, Karyopharm has been at the forefront in evaluating selinexor's efficacy in combination therapies for multiple myeloma, endometrial cancer, and myelofibrosis. The company recently reported long-term follow-up data from a Phase 1/3 study on selinexor in combination with ruxolitinib in myelofibrosis patients, showing promising results in spleen volume and symptom reduction.
Financially, Karyopharm reported total revenue of $33.7 million for Q4 2023, with a full-year revenue of $146.0 million. Despite a competitive market, the company managed to maintain steady growth and focused resources on its high-potential pipeline. With a cash position of $192.4 million as of December 31, 2023, Karyopharm is well-positioned to continue its innovative research and development efforts.
Karyopharm's collaborations with global partners, including Antengene, Menarini, Neopharm, and FORUS, have extended the reach of XPOVIO to various international markets such as Europe, China, South Korea, and Israel. This international expansion underscores the global demand for innovative cancer therapies.
For more information, please visit www.karyopharm.com.
Karyopharm Therapeutics (Nasdaq: KPTI) announced promising results from a Phase 1 study on selinexor combined with ruxolitinib in treatment-naïve myelofibrosis patients. At Week 24, the 60mg dose achieved a 92% SVR35 and 78% TSS50 in the efficacy evaluable population, with 79% SVR35 and 58% TSS50 in the intent-to-treat population. The safety profile was generally tolerable, with common adverse effects like nausea and anemia. Karyopharm is planning to initiate a pivotal Phase 3 study in the first half of 2023 to further explore this combination therapy. Investor interest is high, with a webcast featuring key opinion leader Dr. John Mascarenhas discussing the study's implications. These results could potentially transform treatment options for myelofibrosis.
Karyopharm Therapeutics (NASDAQ: KPTI) announces the presentation of updated data from its Phase 1 study on selinexor, combined with ruxolitinib, to treat treatment-naïve myelofibrosis. These findings will be showcased at the AACR Annual Meeting 2023 in Orlando, Florida, on April 18, 2023. The study's poster session will cover 12 and 24-week data across all patients, including the recommended dose. Additionally, Karyopharm will host an investor webcast on the same day at 4:30 p.m. ET, featuring a key opinion leader discussing the therapy's potential and the unmet medical need in this patient population. Selinexor, marketed as XPOVIO, is a pioneering treatment in the field of oncology, having received regulatory approvals in various countries for multiple cancer indications.
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