Clinical Trials Importance in future therapies. What are the Requirements to Produce New Drugs? Drug must work significantly better than a control treatment.

Slides:



Advertisements
Similar presentations
Randomized Controlled Trial
Advertisements

Single-Patient Use of Investigational Drugs and Biologic Products for Treating Cancer Grant Williams, M.D. Medical Team Leader DODP/CDER/FDA.
Research Study Designs
天 津 医 科 大 学天 津 医 科 大 学 Clinical trail. 天 津 医 科 大 学天 津 医 科 大 学 1.Historical Background 1537: Treatment of battle wounds: 1741: Treatment of Scurvy 1948:
Elements of a clinical trial research protocol
Clinical Trials Medical Interventions
HIV Clinical Trials Janice Price, M.Ed, RN HIV Clinical Research Program Coordinator Swedish Medical Center Seattle, WA USA.
25/5/2009 Dr. Salwa Tayel 1. 25/5/2009 Dr. Salwa Tayel2 Associate Professor Family and Community Medicine Department King Saud University By.
Clinical Trials Hanyan Yang
Pharmaceutical Development and Review Process Rev. 10/21/2014 APGO Interaction with Industry: A Medical Student Guide.
+ Drug Development and Review Process. + Objectives Learn the processes involved in drug discovery and development Define the phases involved in FDA drug.
11/11/04 Clinical Research and Development in the Pharmaceutical and Biotechnology Industry Robert Anderson, MHA, CCRA, CCRCP Director, Clinical Trials.
Experimental Study.
RANDOMIZED CLINICAL TRIALS. What is a randomized clinical trial?  Scientific investigations: examine and evaluate the safety and efficacy of new drugs.
Biomedical research methods. What are biomedical research methods? An integrated approach using chemical, mathematical and computer simulations, in vitro.
INVESTIGATIONAL DRUG SERVICES IN THE HOSPITAL Sheree Miller, Pharm.D. University of Washington Medical Center
Drug trials Learning Outcome: DESCRIBE THE USE OF OPEN LABEL, BLIND AND DOUBLE BLIND TESTS IN HUMAN TRIALS (HIGHER) AND THE USE OF PLACEBOS.
BC Jung A Brief Introduction to Epidemiology - XI (Epidemiologic Research Designs: Experimental/Interventional Studies) Betty C. Jung, RN, MPH, CHES.
Essential Question: How are clinical trials set up to ensure all data collected is valid and that all human subjects are treated ethically?
Clinical Trials. What is a clinical trial? Clinical trials are research studies involving people Used to find better ways to prevent, detect, and treat.
Yesterday, today, and tomorrow
Testing People Scientifically.  Clinical trials are research studies in which people help doctors and researchers find ways to improve health care. Each.
Jasper Ogwal-Okeng Gulu University Research Workshop 3 rd -6 th March 08.
What is a Clinical Trial (alpha version) John M. Harris Jr., MD President Medical Directions, Inc.
Study Design. Study Designs Descriptive Studies Record events, observations or activities,documentaries No comparison group or intervention Describe.
Epidemiology The Basics Only… Adapted with permission from a class presentation developed by Dr. Charles Lynch – University of Iowa, Iowa City.
Stefan Franzén Introduction to clinical trials.
A substance used in the diagnosis, treatment, or prevention of a disease or as a component of a medication A substance used in the diagnosis, treatment,
ECON ECON Health Economic Policy Lab Kem P. Krueger, Pharm.D., Ph.D. Anne Alexander, M.S., Ph.D. University of Wyoming.
Investigational Drugs in the hospital. + What is Investigational Drug? Investigational or experimental drugs are new drugs that have not yet been approved.
Applied Epidemiology Sharla Smith. Discussion Assignments How to complete a discussion assignment –Read the chapters –Evaluate the question –Be very specific.
Research Study Design. Objective- To devise a study method that will clearly answer the study question with the least amount of time, energy, cost, and.
AN INTRODUCTION TO CLINICAL PHARMACOLOGY. BEFORE STARTING DRUG THERAPY, DOCTORS CONSIDER  Whether intervention needed ?  Objective of treatment ? 
Copyright © 2013, 2009, and 2007, Pearson Education, Inc. Chapter 4 Gathering Data Section 4.3 Good and Poor Ways to Experiment.
Experimental Studies Randomized Trials Clinical Trials.
CLINICAL TRIALS IN NEW DRUG DEVELOPMENT Michael A Ross,M.D. President CPL Inc.
 A test of a new intervention or treatment on people.
Lecture 5 Objective 14. Describe the elements of design of experimental studies: clinical trials and community intervention trials. Discuss the advantages.
EXPERIMENTAL EPIDEMIOLOGY
Unit 2 – Public Health Epidemiology Chapter 4 – Epidemiology: The Basic Science of Public Health.
The FDA: Basic Facts It takes 12 to 15 years to develop a single drug Only 1 in 10,000 potential medications makes it completely through the process Only.
بسم الله الرحمن الرحيم جامعة أم درمان الإسلامية كلية الطب و العلوم الصحية - قسم طب المجتمع مساق البحث العلمي / الدفعة 21 Basics of Clinical Trials.
$100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 Terms Clinical Trial Facts.
Is the conscientious explicit and judicious use of current best evidence in making decision about the care of the individual patient (Dr. David Sackett)
C LINICAL R ESEARCH. CONTENTS Drug Development Process Pre – Clinical Studies Clinical Trials Phase I Phase II Phase III Phase IV 2.
Understanding Clinical Trials – Part 2 Georgianne Arnold, MD Professor of Pediatrics University of Pittsburgh Medical Center Pittsburgh Children’s Hospital.
EVALUATING u After retrieving the literature, you have to evaluate or critically appraise the evidence for its validity and applicability to your patient.
What about VIOXX?. Adenomatous Polyp Prevention on Vioxx (APPROVe) Vioxx (rofecoxib) versus Placebo Basic Clinical Trial Objective: Assess whether Vioxx.
Purpose of Clinical Trials Assess safety and efficacy of Experimental treatments New combinations of drugs New approaches to surgery or radiation therapies.
Clinical Trials - PHASE II. Introduction  Important part of drug discovery process  Why important??  Therapeutic exploratory trial  First time in.
Introduction to General Epidemiology (2) By: Dr. Khalid El Tohami.
Clinical Trials and You Ellen Valentine, M.S., CCC-SLP Community Outreach and Education Program Science Park Research Division, Smithville, Texas.
A substance used in the diagnosis, treatment, or prevention of a disease or as a component of a medication recognized or defined by the U.S. Food, Drug,
An Introduction to Clinical Trials and Pharmaceutical Statistics Workshop Robbie Peck University of Bath Student-Led Symposia 16 th Feb 2016.
Section I General principle of Pharmacology. Where can you get information about general principle of Pharmacology?  Text books:  Katzung, Basic and.
The process of drug development. Drug development 0,8 – 1 mld. USD.
Clinical Trials.
Study Development and Design Suzanne Adams RN MPH Director, Clinical Operations Jefferson Clinical Research Institute.
Drug Development Process Stages involved in Regulating Drugs
CLINICAL TRIALS.
The Stages of a Clinical Trial
If you had the power what disease would you like to cure?
Prof. Dr. Basavaraj K. Nanjwade
Clinical Trials Medical Interventions
Randomized Trials: A Brief Overview
Bozeman Health Clinical Research
Clinical Trials.
Is a Clinical Trial Right for Me?
Speeding access to therapies
Introduction to Research Methods in Psychology
Presentation transcript:

Clinical Trials Importance in future therapies

What are the Requirements to Produce New Drugs? Drug must work significantly better than a control treatment Indicated by at least two double-blind randomized controlled clinical trials with 95% power or by three double (triple) -blind randomized controlled clinical trials with 90% power.

Causal Hierarchy Epidemiologists evaluate evidence to determine whether an exposure is directly responsible for an outcome Studies follow a hierarchy in terms of the quality of evidence that they can provide Strongest study is the randomized clinical trial

Introduction to Clinical Trials  Definition  Keywords  Randomized  Placebo Controlled  Blinded  Phases of Clinical Trials  Phase I  Phase II  Phase III  Phase Iv

All clinical trials are prospective studies in which individuals are exposed (or not) and followed for an outcome (or a few different outcomes). The outcomes must be clearly defined. Definition

What’s involved in a clinical trial? 1. Internal Review Board (IRB). Forms need to be filed with the IRB. A committee determines whether the study is ethical. The committee must include some lay people as well as scientists. It should contain an "ethics expert," such as a clergy-person.

2. Protocol. Before conducting a clinical trial, a protocol must be written, describing exactly what you are going to do 3. On site Patient Monitoring and Data collection 4. Data analysis, write results and conclusions 5. Written report: includes clinical and statistical sections

Must have comparability In a clinical trial, need comparability among study groups Best way to assure comparability is by randomization

Examples of confounding Food outbreak: suspect the ham salad, but everyone who ate the ham salad (and only those who ate the ham salad) also ate ice cream. Problem: ham or ice-cream? Observe lower death rate in Alaska than in Florida; conclude sunlight is bad. Problem: people in Florida are older.

Assure comparability by randomization Best way to assure comparability is by randomization

What does randomization do? 1. It forms the basis for the derivation of statistical tests 2. It prevents selection bias by not allowing the physician to decide who to enroll/treat. 3. It minimizes confounding – e.g.: It minimizes the possibility that the observed association between the exposure and the outcome is really caused by a third factor.

Placebo Effects “Inert” substitute for a treatment or intervention “Inert” means the compound has no known activity that would be expected to affect the outcome

Placebo Effects In actuality, a placebo effect is a psychosomatic effect brought about by relief of fears, anxiety or stress because of study participation. It's not just the little white pill that brings about the effect; it's the additional attention and the belief that your condition might be being treated with a superior new treatment. All outcomes affected by psychosomatics are prone to placebo effects.

A component of every specific treatment effect can be attributed to the placebo response. The question that a study should be asking is whether the treatment has any effect on outcome aside from the stress- relieving effect of study participation.

Blinding, also called masking If the outcome can conceivably be affected by patient or investigator expectations, then blinding is important.

Types of Blinding Single Blind: The patient is blind Double Blind: The patient and the investigator are blind Triple Blind: The patient, investigator and data-cleanup people are blind. The statistician can only be partially blinded since he/she has to know which patients are in the same treatment group.

IND: Investigational new drug (device) application Filed prior to beginning clinical trials NDA: New drug application Filed after pivotal trials to get drug (device) approval

1992, 1997 Food and Drug Administration Modernization Act Major drug companies pay a fee of $350,000 when an NDA is submitted. The money is spent to hire a qualified person to review the NDA. Drugs are now approved in less than a year.

Phase 1: Small studies conducted in healthy volunteers. These studies are usually uncontrolled and open labeled. 1. Initial tolerability and safety 2. Pharmacodynamics 3. Dose-finding 4. Pharmacokinetics 5. Bioequivalence studies (these are usually double-blind crossover studies) 6. Food interaction/drug interaction studies

Phase 2. Small to moderate sized trials (usually controlled double or triple blinded) studies in patients. 1. Safety and tolerability 2. Preliminary efficacy. These trials are done with 80% power. 3. Dose-ranging. Find the dose that produces the optimal outcome.

Phase 3. Pivotal clinical trials Two trials with sample size adequate to determine a clinically important difference with 95% power or three trials with sample size adequate to determine a clinically important difference with 90% power are required. For things like blood pressure or cholesterol, sample sizes most often are in the vicinity of per trial (150 to 300 per treatment group). For a drug (does not apply to vaccines), if all trials show a significantly greater effect then placebo, the drug is considered efficacious. The magnitude of the effect does not matter.

Phase IV Post marketing studies: Another hodgepodge of studies, of which clinical trials are a minority. By and large these are descriptive, case-control or cohort studies. 1.Surveillance 2.Answer FDA inquiries 3. Cost effective analyses versus other treatments 4. Validation studies for rating scales 5. Large scale clinical Epidemiology (outcome) studies, usually sponsored by NIH

Summary Clinical trials –Controlled –Randomized –Placebo-controlled –Blinded Phases of clinical trials –Application/ethical approval –Phase I-IV studies

Why participate in a clinical trial? Clinical trials provide opportunity to contribute to development of future therapies Opportunity to test new therapies before they are publicly available

Clinical Trial Opportunities Studies for patients who have never taken PD medication Patients who are advanced and have dyskinesia Patients who are in need of medication