The Cystic Fibrosis Therapeutics Development Network and CF Clinical Research at UNM Jennifer L. Taylor-Cousar, MD Assistant Professor, Adult CF Program/Associate.

Slides:



Advertisements
Similar presentations
Indianapolis Discovery Network for Dementia Comparative Effectiveness Research Trial of Alzheimers Disease Drug: COMET-AD.
Advertisements

Evidence for Transition Programs in Cystic Fibrosis Care Advanced Lung Disease Program : Adult Cystic Fibrosis.
Rare Film Guide Slide Set. Clinical Trial Design for Pirfenidone Study Purpose of Study: To see if the use of pirfenidone decreases the loss of lung function.
429 pharmaceutical care Plan Refa’a AlAjmi. Goal of therpay A goal of therapy is the desired response or endpoint that you and your patient want to achieve.
A5336 A Phase IIa, Double-blind, Placebo-controlled, Randomized Trial of Ruxolitinib in Antiretroviral-treated HIV-Infected Adults CAB Draft Discussion.
EFFICACY AND SAFETY OF RECOMBINANT HUMAN ACTIVATED PROTEIN C FOR SEVERE SEPSIS (PROWESS) GORDONR. BERNARD, M.D. et al. The New England Journal of Medicine.
COPD Research at the University of Maryland School of Maryland COPD Clinical Research Center A member of the National Heart Lung & Blood Institute National.
Cystic Fibrosis Pathogens Activate Ca 2+ -dependent mitogen-activated Protein Kinase Signaling Pathways in Airway Epithelial Cells by Aubrey Osborne and.
2.11 Conduct Medication Management University Medical Center Health System Lubbock, TX Jason Mills, PharmD, RPh Assistant Director of Pharmacy.
Advances in Lung Transplantation: A Patient Guide David J. Lederer, M.D., M.S. Assistant Professor of Medicine New York Presbyterian Lung Transplant Program.
Co-Transporters Na + /Glucose Symport Vibrio cholerae Prokaryote Water-bourne pathogen Produces Cholera Toxin.
Criner et al. NEJM 2014: 370; 23 Simvastatin for the Prevention of Exacerbations in Moderate-to-Severe COPD (STATCOPE) Presented by Ali Naqvi, MD.
Cystic Fibrosis Sharon George PD.3. Cystic Fibrosis is inherited when the child inherits two mutated CFTR genes, one from each parent. The presence of.
Fingolimod Therapy for Multiple Sclerosis
Asymptomatic UC patients on an immunomodulator with persistent moderate mucosal inflammation should either add a biologic or switch to a biologic William.
Blood bank visibility & functionality in the EMR Meghan Delaney, DO, MPH Medical Director, Blood Bank, Seattle Children’s Hospital Assistant Professor,
High-Throughput Screening Speeding Up CF Drug Discovery >10,000 Primary assays/day High-throughput screening CFTR Modulator Drug SAR based Medicinal Chemistry.
Hepatitis C for the General Practitioner Morris Sherman MB BCh PhD FRCP(C) University of Toronto January 2013.
Indianapolis Discovery Network for Dementia Comparative Effectiveness Research Trial of Alzheimer’s Disease Drugs: COMET-AD.
-Cystic Fibrosis (CF) is one of the UK's most common life-threatening inherited diseases. -Cystic Fibrosis affects over 8,500 people in the UK. -Over.
An interdisciplinary approach to care of infants with bronchopulmonary dysplasia. Alfred L. Gest, MD.
Placebo-Controls in Short-Term Clinical Trials of Hypertension Sana Al-Khatib, MD, MHS Assistant Professor of Medicine Division of Cardiology Duke University.
Patient Information - Viral Hepatitis B (HBV)
1 Monitoring The Patient on ARV Treatment HAIVN Harvard Medical School AIDS Initiative in Vietnam.
US Situation Update and CDC International Response H1N1 Pandemic US Situation Update and CDC International Response Peter Nsubuga, MD, MPH On behalf of.
Primary HIV-1 Infection Pathogenesis, Diagnosis, and Treatment Summary of Evidence Martin Markowitz M.D. Clinical Director and Staff Investigator Aaron.
Cystic Fibrosis "Woe to that child which when kissed on the forehead tastes salty. He is bewitched and soon must die." This European adage accurately describes.
MAJOR EVENTS AND EVOLUTION IN CYSTIC FIBROSIS PATIENTS Author: Alexandra Martin Coordinator: Dr. Reka Borka Balas University of Medicine and Pharmacy Târgu-
ASSESSING THE FEASIBILITY OF ANTIBIOTIC MANAGEMENT SERVICES THROUGH PROSPECTIVE EVALUATION ABSTRACT PURPOSE: The inappropriate and unnecessary use of antibiotics.
INPULSIS® trial design and baseline characteristics
PHL 437/Pharmacogenomics First Lecture (Asthma I) By Abdelkader Ashour, Ph.D. Phone:
New Developments in Cystic Fibrosis
A Pharmacokinetic Drug Interaction Study of Drug-72 and Drug-12 Department of Mathematic & Statistics York University Yufeng Lin Xiaofeng Zhou.
Copyright © 2008 Lippincott Williams & Wilkins. Introductory Clinical Pharmacology Chapter 13 Leprostatic Drugs.
Bell Ringer Where does translation occur in the cell? 2.Why do we need RNA to make proteins? 3.How can different codons code for the same amino.
LIVER HEALTH an integral part of CF gastrointestinal care Zachary M Sellers, MD, PhD Fellow Pediatric Gastroenterology, Hepatology, and Nutrition Stanford.
Anemia in CKD The TREAT Trial Reference Pfeiffer MA. A trial of Darbepoetin alpha in type II diabetes and chronic kidney disease. N Engl J Med. 2009;361:2019–2032.
Antibiotics in Addition to Systemic Corticosteroids for Acute Exacerbations of Chronic Obstructive Pulmonary Disease Johannes M.A. Daniels; Dominic snijders;
GASTROENTEROLOGY 2008; 134 :688–695 소화기내과 R4 이 재 연.
Clinical Trials in IPF Dr Helen Parfrey. Are clinical trials needed ? Essential to determine if a drug therapy is beneficial Identify who will benefit.
Tribal Update Lummi Tribal Health Center
Research collaboration in CF
Addition of Inhaled Tobramycin to Ciprofloxacin for Acute Exacerbations of Pseudomonas aeruginosa Infection in Adult Bronchiectasis* Diana Bilton, MD;
Site, Sponsor, CRO: Understanding Roles & Expectations Creating a Team Approach Alan Genatossio, BSN, RN Seattle Children’s, Seattle, WA Colleen.
Improving the Number of Quantity Not Sufficient [QNS] Specimens in Pediatric Cystic Fibrosis [CF] Patients’ Sweat Chloride Testing Christi Dodd, BSN,
Effect of dornase alfa on inflammation and lung function: Potential role in the early treatment of cystic fibrosis  Michael W. Konstan, Felix Ratjen 
April 12, 2017 Guy Reese, Program Integrity Manager
Pseudomonas Lung Infections in Cystic Fibrosis
The Cardiovascular Inflammation Reduction Trial (CIRT)
Patient-Centered Care in Cystic Fibrosis
Advances in Cystic Fibrosis Views and Perspectives From Basel, Switzerland, 2016.
The What, Why and When? of Annual Studies
Evaluating Effects of CFTR Modulation in Cystic Fibrosis
Shoshi Armoni RN, BSN Cystic Fibrosis Center
SIGNIFY Trial design: Participants with stable coronary artery disease without clinical heart failure and resting heart rate >70 bpm were randomized to.
Screening, Lipid Stabilization, and Placebo Run-in
A. Oliver, A. Mena  Clinical Microbiology and Infection 
Cynthia M. Ward, Tara Brinkman, Keith J. Slifer, Shruti M. Paranjape 
Addressing Treatment Challenges in Cystic Fibrosis
Inherited Metabolic Disorders
UK Cystic Fibrosis Registry Annual Data Report 2017
Inhaled Antibiotics for Patients With CF in the Era of CFTR Modulators
A specific database for providing local and national level of integration of clinical data in cystic fibrosis  T. Leal, G. Reychler, P. Mailleux, J. Gigi,
November, 2018 Ljubljana, Slovenia
Inflammatory and immunological biomarkers are not related to survival in adults with Cystic Fibrosis  K.L. Moffitt, S.L. Martin, A.M. Jones, A.K. Webb,
Absence of calf muscle metabolism alterations in active cystic fibrosis adults with mild to moderate lung disease  N. Decorte, M. Gruet, B. Camara, S.
Strategies for Infection Control in Cystic Fibrosis
Experience using centralized spirometry in the phase 2 randomized, placebo-controlled, double-blind trial of denufosol in patients with mild to moderate.
Gene Regulation and Mutation
Chronic Pseudomonas aeruginosa Pneumonia in a Normal Adult
Presentation transcript:

The Cystic Fibrosis Therapeutics Development Network and CF Clinical Research at UNM Jennifer L. Taylor-Cousar, MD Assistant Professor, Adult CF Program/Associate CF Center Director, University of New Mexico CF Center March 19, 2009

CF Therapeutics Development Network (CF TDN) CF TDN –Initially created in 1982 (Research Development Center) –In 2008 made up of 18 centers –With increasing number of potentially therapeutic drugs, it became clear that there were not enough patients at these 18 centers 2 years ago, RFA distributed to increase number of CF research centers In January 2009, UNM became part of the CF TDN

Cystic Fibrosis Therapeutics Development Pipeline

Summary of pH Cascade in CF Altered pH in CF cells Abnormal glycosylation pattern Predisposition to adherence by P. aeruginosa Inflammatory response Chronic lung damage/early death CFTR Mutation PDEi

Sildenafil (Revatio™) in CF CFTRwt ENaC H+H+ Na + Normal cell H+H+ ENaC CFTRm CF cell Inflammation Infection Na + H+H+ ENaC CFTRm CF cell sildenafil CFTRm ENaC H+H+ Na + CF Cell Inflammation Infection

Study Design Placebo-controlled, blinded, randomized cross-over study of sildenafil in clinically stable patients with mild to moderate CF lung disease –Length of participation for each subject will be approximately 15 weeks, and will consist of: Screening visit Two outpatient study visits with initiation of study drug and/or placebo One interim visit during each therapy period (to review concomitant medications and assess side effects) One visit at the end of each therapy period (to reassess inflammatory markers, laboratory studies and side effects) A 28-day washout period with coordinator phone call A follow-up assessment 2 weeks after subject completion