Revenue Performance - Total revenue for Q3 2024 was 38.8million,anincreasefrom36.0 million in Q3 2023[10] - U.S. XPOVIO net product revenue for Q3 2024 was 29.5million,comparedto30.2 million in Q3 2023[10] - License and other revenue for Q3 2024 was 9.3million,upfrom5.8 million in Q3 2023, primarily due to 6.0millionmilestonerevenuefromMenarini[11]−Thecompanynarroweditsfull−year2024totalrevenueguidanceto145.0 million to 155.0million[9]−U.S.XPOVIOnetproductrevenueguidancefor2024isnow110.0 million to 115.0million[9]−TotalrevenueforthethreemonthsendedSeptember30,2024,was38.783 million, an increase from 36.009millioninthesameperiodof2023,representingagrowthof7.783.554 million, down from 86.955millioninthesameperiodof2023,adecreaseof3.536.1 million, slightly up from 35.6 million in Q3 2023, driven by increased clinical trial costs[13] - SG&A expenses for Q3 2024 decreased to 27.6 million from 30.8millioninQ32023duetocostreductioninitiatives[14]−ResearchanddevelopmentexpensesforthethreemonthsendedSeptember30,2024,were36.134 million, compared to 35.553millioninthesameperiodof2023,anincreaseof1.632.1 million for Q3 2024, an improvement from a net loss of 34.5millioninQ32023[17]−Thecompanyreportedanetlossof32.072 million for the three months ended September 30, 2024, compared to a net loss of 34.506millionforthesameperiodin2023,reflectinganimprovementof7.1133.9 million, down from 192.4millionattheendof2023[17]−Thecompanyhadcash,cashequivalents,andinvestmentsof133.526 million as of September 30, 2024, compared to 191.443millionasofDecember31,2023,areductionof30.2189.476 million as of September 30, 2024, from 240.438millionasofDecember31,2023,adeclineof21.2349.123 million, down from $376.644 million as of December 31, 2023, a decrease of 7.3%[32] Clinical Trials and Safety - The Phase 3 SENTRY trial will now use Abs-TSS as a co-primary endpoint, expected to read out top-line data in 2H 2025[6] - The treatment discontinuation rate due to adverse reactions in patients with multiple myeloma receiving XVd was 19%[26] - Fatal adverse reactions in the BOSTON trial occurred in 6% of patients within 30 days of the last treatment[26] Product Approval - Karyopharm's lead compound, XPOVIO, is approved in the U.S. and has received regulatory approvals in various international markets, including Europe and China[28]