,i #aafth ,,congress #ast ,session ,h4 ,r4 #dfbi ,,in ,,the ,,house ,,of ,,representatives ,october #h1 #bjai,mr4 ,tonko 7for himself and ,mr4 ,gibbs7 introduced the following bill2 which was referred to the ,committee on ,energy and ,commerce1 and in addition to the ,committee on ,ways and ,means1 for a period to be subsequently determined by the ,speaker1 in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned ,a ,,bill ,to amend title ,,xviii of the ,social ,security ,act to require the ,secretary of ,health and ,human ,services to add a new set of measures to the #e-star rating system under the ,medicare ,advantage program in order to encourage increased access to biosimilar biological products4 #a4 ,short title ,this ,act may be cited as the ,star ,rating for ,biosimilars ,act4 #b4 ,addition of new measures based on access to biosimilar biological products to the #e-star rating system under medicare advantage 7a7 ,in general ,section #ahec7o77#d7 of the ,social ,security ,act 7#db ,u4,s4,c4 #aciew-#bc7o77#d77 is amended by adding at the end the following new subparagraph3 7,e7 ,addition of new measures based on access to biosimilar biological products 7i7 ,in general ,for #bjba and subsequent years1 the ,secretary shall add a new set of measures to the #e-star rating system based on access to biosimilar biological products covered under part ,b and1 in the case of ,,ma-,,pd plans1 such products that are covered part ,d drugs4 ,such measures shall assess the impact a plan's benefit structure may have on enrollees' utilization of or ability to access biosimilar biological products1 including in comparison to the reference biological product1 and shall include measures1 as applicable1 with respect to the following3 7,i7 ,coverage ,assessing whether a biosimilar biological product is on the plan formulary in lieu of or in addition to the reference biological product4 7,,ii7 ,preferencing ,assessing tier placement or cost sharing for a biosimilar biological product relative to the reference biological product4 7,,iii7 ,utilization management tools ,assessing whether and how utilization management tools are used with respect to a biosimilar biological product relative to the reference biological product4 7,,iv7 ,utilization ,assessing the percentage of enrollees prescribed the biosimilar biological product when the reference biological product is also available4 7ii7 ,definitions ,in this subparagraph1 the terms biosimilar biological product and reference biological product have the meaning given those terms in section #ahdg;,a7c77#f74 7iii7 ,protecting patient interests ,in developing such measures1 the ,secretary shall ensure that each measure developed to address coverage1 preferencing1 or utilization management is constructed such that patients retain equal access to appropriate therapeutic options without undue administrative burden4 4 7b7 ,clarification regarding application to prescription drug plans ,to the extent the ,secretary of ,health and ,human ,services applies the #e-star rating system under section #ahec7o77#d7 of the ,social ,security ,act 7#db ,u4,s4,c4 #aciew-#bc7o77#d771 or a similar system1 to prescription drug plans under part ,d of title ,,xviii of such ,act1 the provisions of subparagraph 7,e7 of such section1 as added by subsection 7a7 of this section1 shall apply under the system with respect to such plans in the same manner as such provisions apply to the #e-star rating system under such section #ahec7o77#d74