Voluntary written informed consentXx_NEWLINE_xXWritten and voluntary informed consent understood, signed and dated.Xx_NEWLINE_xXVoluntary written informed consentXx_NEWLINE_xXWritten and voluntary informed consent.Xx_NEWLINE_xXWritten and voluntary informed consent understood, signed and dated.Xx_NEWLINE_xXVoluntary written informed consent before performance of any study-related procedure not part of normal medical careXx_NEWLINE_xXSigned written informed consent: voluntary written consent must be given before performance of any study-related procedure not part of standard medical careXx_NEWLINE_xXVoluntary written consent signed before performance of any study-related procedure not part of normal medical careXx_NEWLINE_xXVoluntary written consent prior to the performance of any research related proceduresXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consent prior to the performance of any research related proceduresXx_NEWLINE_xXVoluntary written consent prior to the performance of any research related proceduresXx_NEWLINE_xXVoluntary written consent (and assent if donor < 18 years of age) prior to the performance of any research related procedureXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXInability to give voluntary informed consentXx_NEWLINE_xXVoluntary written informed consentXx_NEWLINE_xXVoluntary written consent must be given before performance of any study-related procedure not part of standard medical care. Participants should consent and enter the study within a maximum of 8 weeks of their last dose of ixazomib in the parent study or as agreed by the Millennium clinician/designee.Xx_NEWLINE_xXVoluntary written consent (adult or parent/guardian with presentation of the minor information sheet, if appropriate)Xx_NEWLINE_xXVoluntary written consent before any research related procedures or therapyXx_NEWLINE_xXVoluntary written consent (adult or parent/guardian with presentation of the minor information sheet, if appropriate)Xx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXGives voluntary informed consentXx_NEWLINE_xXWritten and voluntary informed consentXx_NEWLINE_xXVoluntary written consent with appropriate parent/guardian consent and minor information sheet for participants < 18 years of ageXx_NEWLINE_xXVoluntary written consent signed before performance of any study-related procedure not part of normal medical careXx_NEWLINE_xXWritten voluntary informed consentXx_NEWLINE_xXWritten voluntary informed consentXx_NEWLINE_xXWritten voluntary informed consentXx_NEWLINE_xXWritten voluntary informed consentXx_NEWLINE_xXVoluntary written informed consent before performance of any study-related procedure not part of normal medical careXx_NEWLINE_xXVoluntary written informed consent before performance of any study-related procedure not part of normal medical careXx_NEWLINE_xXVoluntary written consent (adult or legally authorized representative; or parental/guardian)Xx_NEWLINE_xXVoluntary written consent prior to the performance of any research related proceduresXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consent (adult or parental/guardian)Xx_NEWLINE_xXVoluntary written consent prior to the performance of any research related proceduresXx_NEWLINE_xXDONORS: Voluntary written consent prior to the performance of any research related procedureXx_NEWLINE_xXVoluntary written informed consent before performance of any study-related procedure not part of normal medical care.Xx_NEWLINE_xXPatient has given voluntary written informed consent before performance of any study-related procedures not part of standard (non-investigational) medical careXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXDONOR: Voluntary written consentXx_NEWLINE_xXInability to give voluntary informed consent or obtain a parent or guardian’s informed consentXx_NEWLINE_xXAbility to understand and provide voluntary written informed consentXx_NEWLINE_xXDONOR: Voluntary written consentXx_NEWLINE_xXDONOR: Voluntary written consentXx_NEWLINE_xXVoluntary written informed consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXAbility to give voluntary informed consent and to comply with treatment and required testsXx_NEWLINE_xXAble and willing to give voluntary, written and signed informed consent before any screening procedure and according to local guidelinesXx_NEWLINE_xXWritten, voluntary informed consent.Xx_NEWLINE_xXAble to sign voluntary written informed consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXGives voluntary informed consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXDONOR: Voluntary written consentXx_NEWLINE_xXVoluntary consent formXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXDONOR: Voluntary written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXDONOR: Voluntary written consentXx_NEWLINE_xXWritten and voluntary informed consentXx_NEWLINE_xXVoluntary written informed consentXx_NEWLINE_xXWilling to provide voluntary written informed consent before performance of any study related procedure not part of normal medical careXx_NEWLINE_xXWritten, voluntary informed consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXAble and willing to give voluntary, written and signed, informed consentXx_NEWLINE_xXInability to give voluntary informed consent or guardian’s informed consentXx_NEWLINE_xXVoluntary, written informed consent.Xx_NEWLINE_xXVoluntary written informed consentXx_NEWLINE_xXDONOR: Voluntary written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary signed, written IRB-approved informed consent.Xx_NEWLINE_xXVoluntary written consent must be given before performance of any study-related procedureXx_NEWLINE_xXVoluntary written informed consentXx_NEWLINE_xXVoluntary written consent must be given before performance of any study-related procedureXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary, signed informed consentXx_NEWLINE_xXAre able to provide voluntary, written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consent (adult or parent/guardian with minor assent for 12 through 17 year olds)Xx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consentXx_NEWLINE_xXVoluntary written consent signed before performance of any study-related procedure not part of normal medical careXx_NEWLINE_xXVoluntary written consent prior to the performance of any research related proceduresXx_NEWLINE_xXVoluntary written consent signed by the subject (or the subject’s legally authorized representative)Xx_NEWLINE_xXAble to give voluntary written informed consentXx_NEWLINE_xX