,,iv #aacth ,,congress #b;d ,session ,h4 ,,res4 #gji ,,in ,,the ,,house ,,of ,,representatives ,july #ca1 #bjad ,mr4 ,vargas 7for himself1 ,mr4 ,rodney ,davis of ,illinois1 ,mr4 ,denham1 ,mr4 ,honda1 ,mr4 ,rush1 and ,ms4 ,matsui7 submitted the following resolution2 which was referred to the ,committee on ,energy and ,commerce ,,resolution ,recognizing the importance of transformative breakthroughs in biomedicine1 biotechnology1 and life sciences in the diagnosis1 management1 curing1 and treatment of illness and the existence of a ,valley of ,death in biotechnology and life sciences funding that stifles innovation and impedes translational medical research4 ,whereas cancer1 rare and orphan diseases1 diabetes1 and ,alzheimer's are just a few of a growing number of large-scale challenges confronting modern society that can be addressed only through the sustained collaboration of thousands of highly skilled1 dedicated1 and independent individuals over many years2 ,whereas many promising breakthroughs have occurred in biomedicine in recent years1 including gene therapies1 molecularly targeted drugs1 new modes of medical imaging and radiosurgery1 biomarkers for drug response1 human genome sequencing1 and advances in bioinformatics that enabled many of these new applications2 ,whereas biomedicine is far more advanced today than even a decade ago is indisputable1 but breakthroughs require years of translational research at a cost of hundreds of millions of dollars and have a substantial likelihood of failure2 ,whereas the drug development pipeline is laden with unfavorable probabilities2 ,whereas for every #e1jjj to #aj1jjj compounds that enter the drug discovery pipeline1 just #bej progress to preclinical development1 and only one will become an approved drug2 ,whereas the aggregate research and development budget of the pharmaceutical industry has nearly doubled from #fh1jjj1jjj1jjj in #bjjb to #abg1jjj1jjj1jjj in #bjaj1 there has been little appreciable impact on the number of new drugs approved2 ,whereas ,congress must work in a bipartisan fashion to reform the ,food and ,drug ,administration's 7,,fda7 review process for drug development and biomedical innovation in order to facilitate expeditious approval of safe and effective new products1 better outcomes for patients1 and more efficient and effective uses of ,,fda's limited resources2 ,whereas biomedical innovation has become much more challenging to finance with private and public equity2 ,whereas there is a growing concern within and outside the industry that the process of translating biomedical research into effective treatments is obsolete2 ,whereas biotech and life sciences traditional financing vehicles of private and public equity are becoming less effective funding sources because the needs and expectations of limited partners and shareholders are not consistent with the increasing complexity and risk of biomedical innovation2 ,whereas the lengthy process of biomedical innovation is becoming increasingly complex1 expensive1 uncertain1 and fraught with conflicting motivations and public-policy implications2 ,whereas industry professionals frequently refer to the ,valley of ,death1 a steadily widening funding and resource gap that currently exists between basic research and clinical development1 effectively limiting the field of potential novel therapies1 technologies1 and treatments for patients2 ,whereas the life sciences industry needs novel approaches to early-stage drug development that better manage risk1 lower capital cost1 improve research effectiveness1 create diverse portfolios1 leverage risk-tolerant capital1 and access new capital sources2 and ,whereas innovative financial structures can achieve the necessary grand scale of capital needed to support effective diversification of biotech investments and create stable and attractive investment opportunities along the development pipeline3 ,now1 therefore1 be it ,that the ,house of ,representatives-- 7#a7 recognizes the importance of transformative breakthroughs in biomedicine1 biotechnology1 and life sciences in the diagnosis1 management1 curing1 and treatment of illness2 7#b7 recognizes the need for bipartisan reform of the ,food and ,drug ,administration 7,,fda7 in order to facilitate expeditious approval of safe and effective new products1 better outcomes for patients1 and more efficient and effective uses of ,,fda's limited resources2 7#c7 recognizes the existence of a ,valley of ,death in biomedicine1 biotechnology1 and life sciences funding1 a steadily widening funding and resource gap that currently exists between basic research and clinical development1 effectively limiting the field of potential novel therapies and drugs for patients2 and 7#d7 recognizes innovative financial structures can achieve the necessary grand scale of capital needed to support translational research and development in biomedicine1 biotechnology1 and life sciences4