CFD RESEARCH CORPORATION — Department of Health and Human Services SBIR Phase I: NHLBI

Description

Abstract The objective of this study is to develop a novel predictive in vitro model for personalized responses to CFTR directed therapeutics This proposal responds to RFA HL Human Cellular Models for Predicting Individual Responses to Cystic Fibrosis Transmembrane Conductance Regulator Directed Therapeutics Cystic fibrosis CF is a life shortening genetic disease caused by loss of function mutations of the Cystic Fibrosis Transmembrane conductance Regulator CFTR gene that encodes an anion channel critical for ion and fluid transport Excellent clinical responses for some individuals e g G D heterozygotes have been seen with ivacaftor a new CFTR directed modulator drug but for the majority of patients benefit has been much less substantial To improve the lives of all CF patients it is crucial that in vivo conditions including the variety of specific mutations and complexity of multi drug therapy as well as pharmacokinetic interactions are faithfully reproduced in an in vitro environment that can be used to rapidly and accurately predict drug efficacy We propose a highly novel in vitro personalized predictive tool on a microfluidics platform utilizing a patient s own cells to target the therapeutic strategy to an individual s complex genetic background and assess full physiological responses to CFTR directed drugs This model will be developed on our commercially available SynVivo family of cell based assays and will mimic the complex airway structure of the CF lung including scale morphology and cellular interactions between the blood the epithelium and the endothelium We will couple this with a novel integrative assessment of CFTR function and airway physiology including multiple aspects of mucus clearance via micro optical coherence tomography in an in vitro environment enabling biologically realistic studies Phase I will culminate with a clear demonstration of the microfluidic platform for physiological responses observed in CF patients with the G D gating mutation During Phase II we will expand the platform by the evaluation of CFTR targeted therapeutics with multi agent therapy and detailed clinical validation A multi disciplinary industry academic partnership with expertise in all areas essential to the successful accomplishment of project goals has been assembled including skilled investigators studying microfluidics cell based assays CF lung physiology drug discovery and development therapeutic screening and clinical studies The end product will be commercialized to pharmaceutical firms drug research labs and universities non profit centers engaged in precision therapeutics drug discovery and drug delivery The primary endpoint is to develop an assay for use as a clinical tool to a priori determine efficacy on a personalized basis for CF patients The overall goal of the proposed effort is to develop and validate a novel in vitro personalized predictive tool on a microfluidic platform utilizing a patient s own cells to target the therapeutic strategy to an individual s complex genetic background and assess full physiological responses to CFTR directed drugs The proposed development will be based on our award winning and commercially available SynVivo family of cell based assays The SynVivo derived from synthetic in vivo model will mimic the physiological structure of the airway including scale morphology cellular interactions between the blood endothelium and the epithelium and airway dynamics in an in vitro environment enabling biologically realistic studies