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June 2020An Innovation -driven Pharmaceutical Company Focused on Improving the Lives of Patients with Cancer and Other Major Diseases
June 2020An Innovation -driven Pharmaceutical Company Focused on
Improving the Lives of Patients with Cancer and Other
Major Diseases2 ©2020 Karyopharm Therapeutics Inc. This presentation contains forward -looking statements within themeaning ofthe“safe harbor” provisions ofThe Private Securities Litigation Reform Actof1995 .Such forward -looking statements
include those regarding Karyopharm’s expectations andplans relating toselinexor asapotential treatment forpatients with multiple myeloma, diffuse large B-celllymphoma, other types ofcancer,
andCOVID -19;thedesign andexecution ofKaryopharm’s clinical trials tostudy selinexor ,including thedosing regimen ;thepotential anti-viral andanti-inflammatory properties ofselinexor ;XPOVIO
forthetreatment ofpatients with heavily pretreated multiple myeloma ;thetherapeutic potential ofandpotential clinical development plans andcommercialization forKaryopharm’s drug candidates,
including thetiming ofinitiation ofcertain trials, ofthereporting ofdata from such trials, ofthesubmissions toregulatory authorities andofpotential commercial launches ;thepotential availability of
accelerated approval pathways ;thepotential sizeofthemarkets formultiple myeloma drugs andmultiple myeloma drugs fortreatment ofpatients withrelapsed multiple myeloma ;thepotential sizeof
themarkets fordiffuse large B-celllymphoma (DLBCL) drugs andDLBCL drugs fortreatment ofpatients withrelapsed and/orrefractory DLBCL ;andKaryopharm’s strategic andfinancial plans and
expectations aswell asfinancial projections forKaryopharm, including 2020 financial guidance andthesufficiency ofcash tofund operatons through mid-2022 .Such statements aresubject to
numerous important factors, risks anduncertainties thatmay cause actual events orresults todiffer materially from Karyopharm’s current expectations .Forexample, there canbenoguarantee that
Karyopharm willsuccessfully commercialize XPOVIO, thatregulators willagree thatselinexor qualifies forconditional approval intheE.U.asaresult ofthedata from theSTORM study inpatients
with penta -refractory myeloma oraccelerated approval intheU.S.based ontheSADAL study inpatients with relapsed/refractory DLBCL orthatanyofKaryopharm’s drug candidates, including
selinexor andeltanexor (KPT -8602 ),Karyopharm’s second generation SINE compound, orKPT-9274 ,Karyopharm’s first-in-class oraldual inhibitor ofPAK4andNAMPT, oranyother drug candidate
Karyopharm isdeveloping, willsuccessfully complete necessary preclinical andclinical development phases orthatdevelopment ofanyofKaryopharm’s drug candidates willcontinue .Further, there
canbenoguarantee thatanypositive developments inthedevelopment orcommercialization ofKaryopharm’s drug candidate portfolio willresult instock price appreciation .Inaddition, even if
Karyopharm receives marketing approval forselinexor inadditional indications orforanyother drug candidate, there canbenoassurance thatKaryopharm willbeable tosuccessfully commercialize
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