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JP Morgan Healthcare Conference January 2019 Targeting Disease at the Nuclear Pore
JP Morgan Healthcare Conference
Targeting Disease at the Nuclear Pore2Forward -looking Statements and Other Important Information
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 thetherapeutic potential ofand potential clinical development plans and commercialization forKaryopharm’s drug
candidates, including thetiming ofinitiation ofcertain trials, ofthereporting ofdata from such trials, ofthesubmissions toregulatory authorities andofpotential commercial
launches, thepotential availability ofaccelerated approval pathways, thepotential sizeofthemarkets formultiple myeloma drugs andmultiple myeloma drugs fortreatment of
patients with relapsed multiple myeloma andKaryopharm’s strategic andfinancial plans andexpectations aswellasfinancial projections forKaryopharm .Such statements
aresubject tonumerous important factors, risks anduncertainties thatmay cause actual events orresults todiffer materially from Karyopharm’s current expectations .For
example, there canbenoguarantee thatregulators willagree thatselinexor qualifies foraccelerated approval intheU.S.orconditional approval intheE.U.asaresult ofthe
data from theSTORM study inpatients with penta -refractory myeloma orSADAL study inpatients with relapsed/refractory DLBCL orthat any ofKaryopharm’s drug
candidates, including selinexor (KPT -330) andeltanexor (KPT -8602 ),Karyopharm’s second generation SINE compound, orKPT-9274, Karyopharm’s first-in-class oraldual
inhibitor ofPAK4 andNAMPT, oranyother drug candidate Karyopharm isdeveloping, willsuccessfully complete necessary preclinical andclinical development phases orthat
development ofanyofKaryopharm’s drug candidates willcontinue. Further, there canbenoguarantee that anypositive developments inKaryopharm’s drug candidate
portfolio willresult instock price appreciation .Inaddition, even ifKaryopharm receives marketing approval forselinexor oranother drug candidate, there canbenoassurance
that Karyopharm willbeable tosuccessfully commercialize that drug candidate. Management’s expectations and, therefore, any forward -looking statements inthis
presentation could also beaffected byrisks anduncertainties relating toanumber ofother factors, many ofwhich arebeyond Karyopharm’s control, including thefollowing :
Karyopharm’s results ofclinical trials andpreclinical studies, including subsequent analysis ofexisting data andnew data received from ongoing andfuture studies ;thecontent
andtiming ofdecisions made bytheFDA andother regulatory authorities, investigational review boards atclinical trialsites andpublication review bodies, including with
respect totheneed foradditional clinical studies ;theability ofKaryopharm oritsthird party collaborators orsuccessors ininterest tofully perform their respective obligations
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