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1 ©2022 KARYOPHARM THERAPEUTICS INC. Fourth Quarter and Full Year 2021 Financial Results & Business Update February 8, 2022
1 ©2022 KARYOPHARM THERAPEUTICS INC.
February 8, 20222 ©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 guidance onits2022 netproduct revenues and2022 non-GAAP research anddevelopment andselling, general andadministrative expenses ;Karyopharm’s expected cash runway ;the
ability ofselinexor oreltanexor totreat patients with multiple myeloma, diffuse large B-celllymphoma, solid tumors andother diseases ;andexpectations related tofuture clinical development and
potential regulatory submissions ofselinexor andeltanexor .Such statements aresubject tonumerous important factors, risks anduncertainties, many ofwhich arebeyond Karyopharm's control, that
may 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 ;orthatanyofKaryopharm’s drug candidates, including
selinexor and eltanexor, willsuccessfully complete necessary clinical development phases orthatdevelopment ofanyofKaryopharm’s drug candidates willcontinue .Further, there canbeno
guarantee thatanypositive developments inthedevelopment orcommercialization ofKaryopharm’s drug candidate portfolio willresult instock price appreciation .Management’s expectations and,
therefore, anyforward -looking statements inthispress release could also beaffected byrisks anduncertainties relating toanumber ofother factors, including thefollowing :theriskthattheCOVID -19
pandemic could disrupt Karyopharm’s business more severely than itcurrently anticipates, including bynegatively impacting sales ofXPOVIO, interrupting ordelaying research anddevelopment
efforts, impacting theability toprocure sufficient supply forthedevelopment andcommercialization ofselinexor orother product candidates, delaying ongoing orplanned clinical trials, impeding the
execution ofbusiness plans, planned regulatory milestones andtimelines, orinconveniencing patients ;theadoption ofXPOVIO inthecommercial marketplace, thetiming andcosts involved in
commercializing XPOVIO oranyofKaryopharm’s drug candidates thatreceive regulatory approval ;theability toobtain and retain regulatory approval ofXPOVIO oranyofKaryopharm’s drug
candidates thatreceive regulatory approval ;Karyopharm's results ofclinical trials andpreclinical studies, including subsequent analysis ofexisting data andnew data received from ongoing andfuture
studies ;thecontent andtiming ofdecisions made bytheU.S.Food andDrug Administration andother regulatory authorities, investigational review boards atclinical trialsites andpublication review
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