Karyopharm reports first quarter 2025 financial results and announces new data in myelofibrosis that further suggests selinexor may lead to meaningful spleen volume reduction, symptom improvement, hemoglobin stabilization and disease modification

– new randomized phase 2 monotherapy data from xport-mf-035 trial in a hard-to-treat patient population further strengthens conviction in selinexor's potential in combination with ruxolitinib in jaki-naÏve myelofibrosis in ongoing phase 3 sentry trial – – phase 3 sentry trial passed planned futility analysis; trial is approximately 80% enrolled with target enrollment expected in june/july 2025 – – demand for xpovio® (selinexor) increased 5% in the first quarter of 2025 compared to the first quarter of 2024; total revenue was $30.0 million; u.s. xpovio® net product revenue of $21.1 million was adversely impacted by a $5.0 million increase in the product return reserve due to atypical returns of expired 80 mg and 100 mg units – – reaffirms full-year 2025 total revenue guidance of $140 million to $155 million, including u.s. xpovio net product revenue guidance of $115 million to $130 million – – company is exploring various alternatives to extend cash runway – –  conference call scheduled for today at 4:30 p.m. et – newton, mass.
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