2016
DOI: 10.3389/fgene.2015.00357
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A Quantitative Assessment of Factors Affecting the Technological Development and Adoption of Companion Diagnostics

Abstract: Rapid innovation in (epi)genetics and biomarker sciences is driving a new drug development and product development pathway, with the personalized medicine era dominated by biologic therapeutics and companion diagnostics. Companion diagnostics (CDx) are tests and assays that detect biomarkers and specific mutations to elucidate disease pathways, stratify patient populations, and target drug therapies. CDx can substantially influence the development and regulatory approval for certain high-risk biologics. Howeve… Show more

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Cited by 8 publications
(9 citation statements)
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“…45 For regulatory approval there is a lack of aligned processes for the constituent components of precision medicine, which causes substantial uncertainty in the potential for return on investment. [46][47][48][49][50][51][52] The advent of tests using NGS is likely to compound regulatory approval of precision medicines. Such issues suggest need for modernized approval mechanisms to guide the required evidence base and address evolving development scenarios.…”
Section: Patient-level Perspectivementioning
confidence: 99%
“…45 For regulatory approval there is a lack of aligned processes for the constituent components of precision medicine, which causes substantial uncertainty in the potential for return on investment. [46][47][48][49][50][51][52] The advent of tests using NGS is likely to compound regulatory approval of precision medicines. Such issues suggest need for modernized approval mechanisms to guide the required evidence base and address evolving development scenarios.…”
Section: Patient-level Perspectivementioning
confidence: 99%
“…Candidate target engagement/proof-of-pharmacology biomarkers include peripheral indicators of inflammation and oxidation for use in trials of anti-inflammatory and antioxidant compounds. Sponsors of drug development should advance markers of target engagement in concert with the candidate therapy; these may be used after regulatory approval as companion or complementary biomarkers [110,111]. Demonstration of target engagement does not guarantee efficacy in later stages of development, but target engagement shown by the "right" biomarker provides important de-risking of a candidate treatment by showing biological activity that may translate into clinical efficacy.…”
Section: The Right Biomarkermentioning
confidence: 99%
“…As a general category, these markers are often referred to as 'companion diagnostics.' [34][35][36] Companion diagnostics have received national press in the past few years because of the Food and Drug Administration's proposal to implement oversight laboratory developed tests, with a particular focus on companion diagnostics. 4,37,38 In head and neck cancer, relatively few companion diagnostic assays are used in the routine clinical setting.…”
Section: Molecular Testing For Therapeutic Decision Makingmentioning
confidence: 99%