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10 Wrapping Up
Pages 73-76

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From page 73...
... In the preclinical arena, participants suggested more effort and funding to develop animal models in which to test investigational drug combinations and their mechanisms of action and pharmacokinetics, as well as resistance mechanisms. These animal models could entail tumor explants or be genetically engineered to develop tumors with the molecular defects commonly seen in human tumors.
From page 74...
... Researchers need to explore more creative innovations in the approach to dosing and scheduling to avoid toxicity and improve efficacy, several participants suggested. Agents could be used intermittently or sequenced in a manner that makes sense from a biological, mechanistic perspective.
From page 75...
... Safe harbors for companies and institutions, such as FNIH and the CEO Roundtable on Cancer Life Sciences Consortium, have proven helpful in negotiating collaborations and managing the patents and other intellectual property rights that result from such collaborations. A safe harbor to distribute study drugs to investigators, or to do preliminary clinical testing of combinations, might substantially further development of combination cancer therapies, many participants stressed.
From page 76...
... Several scientific tools to aid cancer combination therapy development are available in the public domain, including GSK's epigenetic toolbox and preclinical data, NCI's mechanism-of-action assays and preclinical models for combinations, as well as the investigational agents that NCI makes available for preclinical testing. Several participants stressed the importance of doing whatever it takes to facilitate collaboration in the development of combination investi gational cancer therapies.


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