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1 ©2022 KARYOPHARM THERAPEUTICS INC. January 2022A Commercial -Stage Pharmaceutical Company Pioneering Novel Cancer Therapies
1 ©2022 KARYOPHARM THERAPEUTICS INC.
January 2022A Commercial -Stage
Novel Cancer Therapies2 ©2022 KARYOPHARM THERAPEUTICS INC. Forward -looking Statements and Other Important Information
This presentation contains forward -looking statements within themeaning ofThe Private Securities Litigation Reform Actof1995 .Such forward -looking statements include those regarding Karyopharm’s
preliminary financial information forfourth quarter andfullyear 2021 ;guidance onitsexpected cash runway and2022 research anddevelopment expenses ;expectations toprovide annual revenue guidance
during Q12022 ;expectations andplans relating toXPOVIO oranyofitsdrug candidates, ifapproved, forthetreatment ofadult patients with relapsed orrefractory multiple myeloma orrelapsed orrefractory
diffuse large B-celllymphoma andother hematologic malignancies andsolid tumors ;commercialization ofXPOVIO oranyofitsdrug candidates, ifapproved, andthecommercial performance ofXPOVIO ;
submissions to,andthereview andpotential approval ofselinexor oranyofitsother drug candidates by,regulatory authorities, including theCompany’s regulatory strategy, theanticipated availability ofdata to
support such submissions, timing ofsuch submissions andactions byregulatory authorities andthepotential availability ofaccelerated approval pathways ;theexpected design oftheCompany’s clinical trials ;
andthetherapeutic potential ofandpotential clinical development plans forKaryopharm's drug candidates, especially selinexor andeltanexor .Such statements aresubject tonumerous important factors, risks
anduncertainties, many ofwhich arebeyond Karyopharm's control, thatmay cause actual events orresults todiffer materially from Karyopharm's current expectations .Forexample, there canbenoguarantee
thatKaryopharm willsuccessfully commercialize XPOVIO ;thatregulators willgrant confirmatory approval intheEuropean Union based ontheBOSTON study inadult patients with multiple myeloma ;orthat
anyofKaryopharm’s drug candidates, including selinexor andeltanexor, willsuccessfully complete necessary clinical development phases orthatdevelopment ofanyofKaryopharm’s drug candidates will
continue .Further, there can benoguarantee that any positive developments inthedevelopment orcommercialization ofKaryopharm’s drug candidate portfolio willresult instock price appreciation .
Management’s expectations and, therefore, anyforward -looking statements inthispresentation could also beaffected byrisks anduncertainties relating toanumber ofother factors, including thefollowing :the
riskthattheCOVID -19pandemic could disrupt Karyopharm’s business more severely than itcurrently anticipates, including bynegatively impacting sales ofXPOVIO, interrupting ordelaying research and
development efforts, impacting theability toprocure sufficient supply forthedevelopment andcommercialization ofselinexor orother drug candidates, delaying ongoing orplanned clinical trials, impeding the
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