Research based, people driven CDISC ADaM Datasets - from SDTM to submission CDISC Experience Exchange and ADaM Workshop 15 Dec 2008 Zoë Williams, LEO Pharma.

Slides:



Advertisements
Similar presentations
Dimitri Kutsenko (Entimo AG)
Advertisements

CDISC based eSubmission Key Points of the CDISC SDTM/ADaM Pilot
Principal Statistical Programmer Accovion GmbH, Marburg, Germany
SDTM Implementation Guide Version 3.1.2
ADaM Implementation Guide: It’s Almost Here. Are You Ready?
Quick tour of CDISC’s ADaM standard
Copyright © 2013, SAS Institute Inc. All rights reserved. LEVERAGE THE CDISC DATA MODEL TO STREAMLINE ANALYTICAL WORKFLOWS KELCI J. MICLAUS, PH.D. RESEARCH.
Change/Insert Date & Location via >Insert >Header & Footer 1. Check in Date & Time 2. Type under >Fixed 3. Check in Footer 4. Fill in field 5. Click Apply.
ADaM Standards Wouter van Wyk. Why ADaM –SDTM purpose is to provide collected data Not designed for ease of analysis –ADaM purpose is to provide data.
Life Sciences Accelerated R&D Services The Science of Getting Products to Patients Faster Study Data Standardization Plan Use Case Experience Dave Izard.
Moving from US FDA focus to Global focus – Importance of Standards Margaret Minkwitz Sept 16, 2010.
CDISC and how Stata can help us implement it
Beyond regulatory submission - Standards Metadata Management Kevin Lee CDISC NJ Meeting at 06/17/2015 We help our Clients deliver better outcomes, so.
23 August 2015Michael Knoessl1 PhUSE 2008 Manchester / Michael Knoessl Implementing CDISC at Boehringer Ingelheim.
Dominic, age 8, living with epilepsy SDTM Implementation Guide : Clear as Mud Strategies for Developing Consistent Company Standards PhUSE 2011 – CD02.
JumpStart the Regulatory Review: Applying the Right Tools at the Right Time to the Right Audience Lilliam Rosario, Ph.D. Director Office of Computational.
A Taste of ADaM Presented by: Peng/Zik Liu MSD (Shanghai) Pharma Co.
CBER CDISC Test Submission Dieter Boß CSL Behring, Marburg 20-Mar-2012.
© 2011 Octagon Research Solutions, Inc. All Rights Reserved. The contents of this document are confidential and proprietary to Octagon Research Solutions,
PhUSE SDE, 28-May A SAS based Solution for define.xml Monika Kawohl Statistical Programming Accovion.
Remapping of Codes (and of course Decodes) in Analysis Data Sets for Electronic Submissions Joerg Guettner, Lead Statistical Analyst Bayer Pharma, Wuppertal,
Qualification Process for Standard Scripts Hosted in the Open Source Repository ABSTRACT Dante Di Tommaso 1 and Hanming Tu 2 Tehran 1 F. Hoffmann-La Roche.
Implementation of a harmonized, report-friendly SDTM and ADaM Data Flow General by Marie-Rose Peltier Experience by Marie Fournier Groupe Utilisateurs.
© 2008 Octagon Research Solutions, Inc. All Rights Reserved. 2 Octagon Research Solutions, Inc. Leading the Electronic Transformation of Clinical R&D ©
Antje Rossmanith, Roche 14th German CDISC User Group, 25-Sep-2012
1CDISC 2002 RCRIM – Standard Domains Agenda NCI Presentation Standard Domains Working Group Goals Introduction to FDA Information Model (FIM) Discussion:
Overview and feed-back from CDISC European Interchange 2008 (From April 21 st to 25 th, COPENHAGEN) Groupe des Utilisateurs Francophones de CDISC Bagneux.
Confidential - Property of Navitas Accelerate define.xml using defineReady - Saravanan June 17, 2015.
MODULE B: Case Report Forms Jane Fendl & Denise Thwing April 7, Version: Final 07-Apr-2010.
Second Annual Japan CDISC Group (JCG) Meeting 28 January 2004 Julie Evans Director, Technical Services.
© Copyright 2008 ADaM Validation and Integrity Checks Wednesday 12 th October 2011 Louise Cross ICON Clinical Research, Marlow, UK.
How to go from an SDTM Finding Domain to an ADaM-Compliant Basic Data Structure Analysis Dataset: An Example Qian Wang, MSD, Brussels, Belgium Carl Herremans,
SDTM Validation Delaware Valley CDISC user network Ketan Durve Johnson and Johnson Pharmaceutical Reasearch and Development May 11 th 2009.
Alun, living with Parkinson’s disease QS Domain: Challenges and Pitfalls Knut Müller UCB Biosciences Conference 2011 October 9th - 12th, Brighton UK.
CONFIDENTIAL The Ultimate Integration Challenge Jennifer Chin, Covance Hester Schoeman, Covance PhUSE Conference Berlin 2010 Paper DH06.
SAS Programmer in Teva Pharmaceuticals Job Description The basic responsibilities are to provide SAS programming support in deriving analysis datasets,
Implementation of CDISC Standards at Nycomed PhUSE, Basel (19-21 October 2009) Nycomed GmbH, Dr. B Traub CDISC Implementation at Nycomed.
Overview of CDISC standards and use cases along the E2E data management process Dr. Philippe Verplancke ESUG Marlow, UK 27 May 2009.
Optimizing Data Standards Working Group Meeting Summary
CDISC©2009 February CDISC INTRAchange Carey Smoak Device Team Leader Li Zheng Submission Data Standards Team Member Thurday, April 2, 2009.
Preventing Wide and Heavy ADs Dirk Van Krunckelsven Phuse 2011, Brighton ADaM on a Diet.
From PDF to RDF – Representing the CDISC Foundational Standards
© 2011 Clinovo. All Rights Reserved. The contents of this document are confidential and proprietary to Clinovo 1 Clinovo 1208 E. Arques Avenue, Suite 114.
Research Study Data Standards Standards for research study data for submission to regulatory authorities Standard development divided into three parts:
Copyright © 2015, SAS Institute Inc. All rights reserved. Future Drug Applications with No Tables, Listings and Graphs? PhUSE Annual Conference 2015, Vienna.
Corporate Data Vault Data Warehousing Workshop Sept Data Warehousing Workshop Sept
1 Much ADaM about Nothing – a PROC Away in a Day EndriPhUSE Conference Rowland HaleBrighton (UK), 9th - 12th October 2011.
April ADaM define.xml - Metadata Design Analysis Results Metadata List of key analyses (as defined in change order) Analysis Results Metadata per.
UC3: Complications Related to Unscheduled performed instead scheduled (TK) Raw visit numberVISITNUMLBDYLBDTC 2missing VISITVISITNUMSVDYSVDTCSVUPDES.
1. © CDISC 2014 Presented by Angelo Tinazzi, Cytel Inc, Geneva, Switzerland Presented at 2014 CDISC Europe Interchange, Paris Adapted for CDISC UK Network.
How Good is Your SDTM Data? Perspectives from JumpStart Mary Doi, M.D., M.S. Office of Computational Science Office of Translational Sciences Center for.
MindMajix SAS Clinical TrainingSAS Clinical Training.
ADaM or SDTM? A Comparison of Pooling Strategies for Integrated Analyses in the Age of CDISC Joerg Guettner, Lead Statistical Analyst, Bayer Pharma, Wuppertal,
Mark Wheeldon, Formedix CDISC UK Network June 7, 2016 PRACTICAL IMPLEMENTATION OF DEFINE.XML.
Clinical database management: From raw data through study tabulations to analysis datasets Thank you for your kind introduction, and the opportunity to.
Building Block macro principle for Standard Program Library Design
Secondary Uses Primary Use EHR and other Auhortities Clinical Trial
Beyond regulatory submission - Standards Metadata Management Kevin Lee CDISC NJ Meeting at 06/17/2015 We help our Clients deliver better outcomes, so.
Accenture Accelerated R&D Standards Metadata Management – version control and its governance Kevin Lee CDISC NJ Meeting at 01/28/2015 We help our Clients.
SDTM Work Stream Basel, September 2, 2008.
Why use CDISC for trials not submitted to regulators?
Creating ADaM Friendly Analysis Data from SDTM Using Meta-data by Erik Brun & Rico Schiller (CD ) H. Lundbeck A/S 13-Oct
Traceability between SDTM and ADaM converted analysis datasets
In-Depth Report from Optimizing Data Standards Working Group
Patterns emerging from chaos
Fabienne NOEL CDISC – 2013, December 18th
SDTM and ADaM Implementation FAQ
An FDA Statistician’s Perspective on Standardized Data Sets
SDTM Work Stream Basel, September 2, 2008.
Safety Analytics Workshop – Computational Science Symposium 2019
Presentation transcript:

research based, people driven CDISC ADaM Datasets - from SDTM to submission CDISC Experience Exchange and ADaM Workshop 15 Dec 2008 Zoë Williams, LEO Pharma

research based, people driven 2 Summary  Background  ADaM datasets  Process  Conclusions

research based, people driven 3 Project Background  Therapeutic area – dermatology – psoriasis  Baseline, Efficacy, Safety data  Categorical & continuous efficacy data  Imputed values for missing data

research based, people driven 4 Project  16 phase 1, 2 and 3 studies  Baseline and safety – 16 studies  Efficacy – 7 studies  4500 patients  Majority of studies already reported from non-ADaM datasets  Some ongoing studies still to be reported  Data Management provided SDTM datasets

research based, people driven 5 ADaM Dataset Planning ADaM guidelines Previous ADaMs New Thinking ADaM Specification Practical Use

research based, people driven 6 ADaM Specification Example ADSL: SUBJECT LEVEL ANALYSIS DATASET [ADSL.xpt] 1 record / USUBJID Variable name LabelTy pe Format (codes) OriginRoleComments STUDYIDStudy Identifier ChDM.STUDYIDIdentifier USUBJIDUnique Subject Identifier ChDM.USUBJIDIdentifier RANDRandomised Population Flag ChY or NDerived from SUPPQUAL.QVAL (where QNAM=RAND) Selection SAFETYSafety Population Flag ChY or NDerived from SUPPQUAL.QVAL (where QNAM=SAFETY) SelectionStudy XXX flag is for Induction Phase TRTSTDTStart Date of Treatment DtDerived from EX.EXSTDTC TimingConverted to SAS date AGEGRPAge GroupCh≤ ≥65 Derived from DM.AGEResults Qualifier, Analysis

research based, people driven 7 ADaM Datasets  Approx. 100 study ADaM datasets  Datasets relevant to each study ADSL Drug Acc. 4 EfficacyDisposition Labs3 Adverse Event Exposure Vital Signs

research based, people driven 8 Considerations  Order of variables  Flags  Missing values  Dependencies between datasets  >1 record per patient  One or many datasets  Efficacy/adverse events  ‘Analysis ready’ / ‘One proc away’

research based, people driven 9 Process – Ongoing Studies SDTM ADaM dataset Tables, Figures, Listings Clinical Study Report ADaM.xptDocumentation Electronic submission

research based, people driven 10 Process – Conversion SDTM ADaM dataset Tables, Figures, Listings Clinical Study Report ADaM.xptDocumentation Electronic submission Oracle Clinical ® dataset

research based, people driven 11 Pooled ADaM Datasets  13 pooled ADaM datasets  Data from each relevant study ADSL Drug Acc. EfficacyDisposition LabsAdverse Event Exposure

research based, people driven 12 Pooled Data Documentation Electronic submission ADaM – study 1 ADaM – study 2 ADaM – study 3 ADaM – study n Tables/Analysis Clinical Summaries ADaM – S1 ADaM – S2 ADaM – S3. ADaM - Sn Added Variables Pooled ADaM

research based, people driven 13 Development  Great to have new version of ADaM guidelines  More specific  Hopefully easier to implement  Creating Global Library for Metadata instead of specifications  Use across projects  Standard  Programs/macros  Process  Training to support new process

research based, people driven 14 Challenges  SDTM/ADaM format new  Learning curve  Concept  Terminology  Documentation  Variation in interpretation  Need to use ADaM format?  Additional work  Studies already reported  Additional work/QC

research based, people driven 15 Benefits  Familiarity with CDISC  Sceptics became converts  Pooled data more straightforward  Use of ADaMs now accepted as standard  Submission ready data

research based, people driven 16 Conclusions  CDISC ADaM format usable  Accepted by FDA – now requesting them  Quicker implementation -> less work in future  ADaM is a different data format which can be used as well as any other – need to manage the change

research based, people driven Questions

18

research based, people driven Facilitated Discussion

research based, people driven 20 Individuals (5 minutes)  Beginners  List main (suggest 3) items that you (your company) require to be able to start using ADaM.  Users  List main (suggest 3) items that you (your company) require to be able to take use of ADaMs forward.

research based, people driven 21 Table Discussion (10/15 mins)  Pool/discuss items to create pooled list  Identify the most common

research based, people driven 22 Group Discussion (20/25 minutes)  Take most common issues in turn from each table for discussion

research based, people driven 23 FDA experience (15 mins)  Any discussion with FDA  Prior to submission  After submission  Requests  Feedback