VICH Task Force for Efficacy Studies for Combination Products Progress Report for the 32 th SC /6 th VOF meeting (Final)

Slides:



Advertisements
Similar presentations
EPAA Annual conference November Regulatory acceptance of alternative approaches for pharmaceuticals Jean-Marc Vidal Safety & Efficacy of Human Medicines.
Advertisements

OIE First Global Conference on Veterinary Legislation 1 Control of Veterinary Products: The Need for Global Standards Merton V. Smith, Ph.D., J.D. Director,
Research & Innovation Evolution from IMI1 to IMI2: challenges ahead Elmar Nimmesgern, PhD DG Research & Innovation 1.
Environment case Episode 3 - CAATS II Final Dissemination Event Brussels, 13 & 14 Oct 2009 Hellen Foster, Jarlath Molloy NATS, Imperial College London.
WHO Training Course on Prequalification Introduction Efficacy and Safety Issues Hans Kemmler Consultant to WHO Accra, 5.Nov
Integrating CMC Review & Inspection Industry Recommendations Joe Anisko April 24, 2003.
The ICH E5 Question and Answer Document Status and Content Robert T. O’Neill, Ph.D. Director, Office of Biostatistics, CDER, FDA Presented at the 4th Kitasato-Harvard.
Effectiveness Evaluation for Therapeutic Drugs for Non-Food Animals
U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only.
Clinical Trials of Traditional Herbal Medicines In India Y.K.Gupta Professor & Head, Department of Pharmacology, All India Institute of Medical Sciences,
TANZANIA August Note on Choice of Comparator Products: Current status Note to Applicants on Choice of Comparator Products in the Prequalification.
Training Workshop on Pharmaceutical Development with a Focus on Paediatric Medicines / October |1 | Regulatory Requirement on Dossier of Medicinal.
Good Clinical Practice GCP
3rd Baltic Conference on Medicines Economic Evaluation, Reimbursement and Rational Use of Pharmaceuticals Pricing and Reimbursement of Pharmaceuticals.
Whilst the pharmaceutical industry plays a key role in developing and producing medicines, there is a tension between industry’s need to expand product.
Exploratory IND Studies
Artemisinin combined medicines, Kampala, February |1 | Training workshop on regulatory requirements for registration of Artemisinin based combined.
Anthelmintics Or ‘Why I like drugs” Nick Sangster Faculty of Veterinary Science University of Sydney.
Review of veterinary medicines legislation in 2010 Mario Nagtzaam Unit F2 „Pharmaceuticals“ Directorate-General Enterprise and Industry European Commission.
44th GRSP Session Status report of Informal Group on FI Pierre CASTAING Chairman Informal Document No. GRSP (44th session, December 2008, agenda.
WHO Workshop on Assessment of Bioequivalence Data Addis Ababa, 31. August – 3. September 2010 Selection of comparators Compiled by Jan Welink WHO Workshop.
EC actions against the rising threats from Antimicrobial Resistance
TANZANIA AUGUST TRAINING WORKSHOP ON PHARMACEUTICAL QUALITY, GOOD MANUFACTURING PRACTICE AND BIOEQUIVALENCE WITH A FOCUS ON ARTEMISININS.
Deficiencies in Bioequivalence dossiers Overview and Examples.
FDA Advisory Committee for Pharmaceutical Science and Clinical Pharmacology July 22-23, 2008 Introduction and Update Helen N. Winkle Director, Office of.
Creating the environment for business Assessment of the Implementation by the Member States of the IPPC Directive Advisory Group Meeting Friday 13 th January.
Role of VICH and VICH guidelines in the approval process for veterinary medicinal products David Mackay, European Medicines Agency VICH Workshop – Dar.
Application of VICH GLs – extract from group discussion General: VICH GLs do not prescribe the data package to be submitted for registration, they merely.
JMAFF (Chair of Biologicals Quality Monitoring EWG)
VICH Guidelines: Stability Testing of New Veterinary Drug Substances and Medicinal Products Mai Huynh U.S. FDA Center for Veterinary Medicine Washington.
VICH General Principles and current update of VICH Outreach Forum activity 1.
Health and Food Safety EU strategy for Pharmaceuticals in the Environment Patrizia Tosetti DG SANTE European Commission China/EU Pharmaceutical Industry.
VICH Training Strategy Steven D. Vaughn, DVM Director, Office of New Animal Drug Evaluation, Center for Veterinary Medicine U.S. Food and Drug Administration.
Introduction to the VICH Outreach Forum Steven D. Vaughn, DVM VICH Workshop Dar Es Salaam, Tanzania – June 24, 2015.
-What is VICH, History and Objectives Hervé MARION, DVM VICH Secretariat.
1 VICH AND VETERINARY MEDICINES AVAILABILITY VICH5 CONFERENCE, OCTOBER 2015, TOKYO VICH AND VETERINARY MEDICINES AVAILABILITY VICH5 CONFERENCE, OCTOBER.
Session 3: How to use VICH GLs VICH5 Conference, October 2015, Tokyo 1.
An agency of the European Union Principles for the assessment and authorisation of antimicrobials in the EU VICH Outreach Forum, October 2015 Presented.
Abstract A step-wise or ‘tiered’ approach has been used as a rational procedure to conduct environmental risk assessments in many disciplines. The Technical.
VICH Outreach Forum OIE contribution 2 nd meeting of the Forum members Washington, 19 – 20 February 2013 S. Munstermann, JP Orand, C. Lambert.
Compassionate use programs and the European regulatory system Filip Josephson M.D., Ph.D. Clinical Assessor.
New data collection-State of play Residues of Veterinary Medicinal Products in live animals and animal products Anca Stoicescu, Scientific Officer Zagreb,
Link between legal framework of VMP regulation and VICH GLs in Japan Takashi Kozasa DVM Ministry of Agriculture, Forestry and Fisheries Government of Japan.
Session 9: The Vision for the Future 1 Dr. Yuko Endo JMAFF.
Session 7: VICH Conference
How to comment VICH guidelines Shixin XU, PhD, Prof. China IVDC.
VICH Task Force for Efficacy Studies for Combination Products Progress Report (Final) VICH members JMAFF (chair)K. Noda JVPAE. Oishi IFAH-EUM. Bobey EUK.
1 THE OIE REPORT 32 nd VICH SC Meeting / 6 th VICH Outreach Forum Meeting Jean-Pierre Orand, Anses, France, OIE Collaborating Centre.
How to get involved in VICH Dr. Allen Bryce Independent consultant Canberra, Australia VICH Workshop: Dar Es Salaam, Tanzania – 24.
Waiving TABST for vaccines Argentina: Not an allowed procedure today Require batch safety tests in laboratory animals, repeated by authorities Currently.
1 1 Topics “out of the scope of VICH” Brigitte Boenisch IFAH-Europe 2 nd VICH Outreach Forum Meeting Washington, 19 th /20 th February 2012 – how and by.
1 The contribution of VICH to the global One Health approach VICH5 CONFERENCE, OCTOBER 2015, TOKYO Jean-Pierre Orand, Anses, France, OIE Collaborating.
Update of Results of the Survey on training Priorities
POST APPROVAL CHANGE MANAGEMENT PROTOCOLS IN THE EUROPEAN UNION
Hervé Marion, DVM VICH Secretariat
VICH General Principles and
Pre-Investigational New Drug (pre-IND) Meeting with FDA
The Vision for the Future
Report by the VICH Steering Committee on issues raised by Forum members during the 1st Outreach Forum meeting Hervé Marion, DVM VICH Secretariat.
Multinational collaboration in the Authorisation of VMPs: the EU approach VICH Outreach Forum Tokyo, Nov 2017 Noel Joseph European Commission.
Waiving Target Animal Batch Safety Testing for vaccines
The Benefits of VICH to Emerging Countries
GL50(R)- HARMONISATION OF CRITERIA TO WAIVE TARGET ANIMAL BATCH SAFETY TESTING FOR INACTIVATED VACCINES FOR VETERINARY USE ( May 2017) GL55- HARMONISATION.
Developments in the EU medicines regulatory network
Quality guidelines on impurities
GL8 (R) – Stability testing for medicated premixes
Hervé Marion, DVM VICH Secretariat
VICH GL 54, Studies to evaluate the safety of residues of veterinary drugs in human food: General approach to establish an Acute Reference Dose (ARfD)
Control of Veterinary Drugs in South Africa
Presentation transcript:

VICH Task Force for Efficacy Studies for Combination Products Progress Report for the 32 th SC /6 th VOF meeting (Final)

Introduction  At the 3 rd VOF meeting in Nov 2013, China PR presented a Concept Paper for a VICH guideline on “efficacy studies for combination drug products”.  The SC & VOF members welcomed the proposal confirming that it is an important topic where guidance is currently lacking.  The scope of this topic is very broad and could lead to several GLs.  It would be useful to identify the different combinations available in order to reach agreement on which GLs should be developed. The SC decided to create a task force (TF) chaired by JMAFF.

Mandate for TF  To elaborate a discussion paper proposing a more focused scope for the development of a VICH GL for efficacy studies for combination products. <<< Concept paper from China  The TF will  Prioritize the target products  Explore the possibility of a general policy document >Explore Major combination >Analyse GLs already in Place

TF members VICH members JMAFF (chair)K. Noda JVPAE. Oishi IFAH-EUM. Bobey EUK. Healey US FDAC. Groesbeck AHIB. McKusick Observer South Africa, Nat. Dept. healthV. Naidoo VOF members China PR, IVDCS. Xu Argentina, SENASAL. Sbordi Taiwan, Council of AgricultureT-R. Jan UEMOAK.Th. Domagni CAMEVETL. Sbordi Additional contributors Australia, APVMAP. Reeves NZ, Min. Primary IndustryW. Hughes

Part 1 Major Combination

How to categorize the products? Categorization elements Code Antiparasitics AnthelminticsAP-Hl AntiprotozoalsAP-Pr EctoparasiticidesAP-Ec EndectocidesAP-EnEc Other AntiparasiticsAP-X Antimicrobials AntibacterialsAM-Bc AntimycoticsAM-Mc AntiviralsAM-Vr Intramammary antibacterials AM-IM-Bc Other AntimicrobialsAM-X Anti-inflammatoriesAI AntisepticsAS DisinfectantsDI (others, if any)X

Combination-category VICH membersObserverVOF members Sub- total Total JMAFFJVPAEU IFAH- EU US FDAAHIS.AfricaAsust.NZChinaPR Argentina/ CAMEVET TaiwanUEMOA AP-Hl AP-Pr AP-Ec AP-EnEc AP-HlAP-Pr 11 2 AP-HlAP-Ec AP-HlAP-EnEc 1 1 AP-HlAP-x AP-HlX 1 1 AP-EcAP-x 1 1 AP-EnEcAP-x 1 1 AM-Bc AM-Mc 0 AM-Vr 0 AM-IM-Bc AM-BcAM-Mc 0 AM-IM-BcAM-Bc 1 1 AM-McAI AM-BcAI AM-BcAI Analgesics 1 1 AM-BcAP-Pr AM-BcHormones 1 1 AI AS 1 11 DI Vitamins1 11 Minerals1 11 Gastrointestinal1 11 Hormones Cardiology X 1 11 Total / legislation Total / member status Major combination-products

Major Combination-products

Combination category Ingredients Number of Country/Region AP-HI Abamectin +Derquantel 1 Abamectin +albendazole +selenium +cobalt 1 Albendazole +closantel, 1 Emodepside +Praziquantel 3 Fenbendazole +levamisole, 1 Fenbendazole+Praziquantel 1 Febantel+pyrantel 1 Febantel +Praziquantel +Pyrantel 5 Ivermectin +Clorsulon 2 Ivermectin +closantel 1 Ivermectin+pyrantel 1 Levamisole +Abamectin, 1 Levamisole +Albendazole, 1 Levamisole +closantel +albendazole +abamectin, 1 MilbemycinOxime+praziquantel 1 Moxidectin+triclabendazole 1 Oxfendazole +Levamisole, 1 AP-Pr Amprolium +ethopabate, 1 Amprolium +Ethopabate +Sulfaquinoxaline 2 Dinitolmide+glycarbylamide 1 Pyrimethamine+sulfadimethoxine 1

Combination category Ingredients Number of Country/Region AP-Ec Amitraz+Fipronil+(S)-methoprene 1 Amitraz +cypermethrin, 1 Amitraz+Metaflumizone 1 Betacyfluthrin +piperonyl butoxide, 1 Cipermethrin+ethion 1 Cymiazol +cypermethrin, 1 Diazinon +pyriproxyfen, 1 Dicyclanil +diflubenzuron, 1 Dinotefuran+permethrin+pyriproxyfen 1 Fipronil+cyphenothrin 1 Fipronil+(S)-methoprene 1 Fipronil+permethrin 1 Imidacloprid+flumethrin 1 Imidacloprid+moxidectin 1 Imidacloprid +permethrin, 1 Imidacloprid+permethrin+piperonyl butoxide 1 Indoxacarb+permethrin 1 Pyrethrins +piperonyl butoxide 1 AP-EnEc Abamectin +levamisole,1 Abamectin +praziquantel, 1 Closantel+ivermectin 1 Closantel+mebendazole, 1 Clorsulon+Ivermectin 1 Eprinomectin+fipronil+praziquantel+(S)-methoprene 1 Fluazuron +ivermectin, 1 Imidacloprid+Ivermectin, 1 Imidacloprid+Moxidectin, 3 Ivermectin+Pyrantel 2 Ivermectin+Praziquantel, 2 Milbemycin+Spinosad 1 MillbemycinOxime+Lufenuron 3 MilbemycinOxime+Lufenuron+Praziquantel 2 MilbemycinOxime+spinosad 1

Combination category Ingredients Number of Country/Region AP-HlAP-Pr Emodepside+toltrazuril 1 AP-HlAP-Ec Emodepside+praziquantel 1 Fipronil+methoprene+amitraz 1 Ivermectin+albendazole 1 Narasin+nicarbazin 1 AP-HIAP-EnEc Levamisole HCI +praziquantel, 1 Levamisole HCI +oxyclosanide, 1 Albendazole +closantel, 1 Levamisole HCI +rafoxanide, 1 AP-HIX Levamisole +Sodium Selenate, 1 Albendazole +Sodium Selenate, 1 Abamectin +Sodium Selenate, 1 Levamisole +Disodium Cobalt EDTA, 1 AP-HlAP-x Albendazole+praziquantel 1 fenbendazole+praziquantel+pyrantel 1 MilbemycinOxime+lufenuron, 1 MilbemycinOxime+lufenuron+Praziquantel 1 AP-EcAP-x Moxidectin + imidacloprid, 1 Ivermectin + closantel, 1 AP-EnEcAP-x abamectin+Ivermectin 1 clorsulon+Ivermectin 1 Ivermectin+nitroxinil 1

Specific consideration #1  The EU member insisted not to include AM combination as a target category, supported by other countries.  Regulators do not wish to encourage new developments of AM combination.  A VICH GL on such combination products could be misunderstood as encouragement for their development.

Specific consideration #2  Antimicrobial agents and coccidiostats for “growth/ feed efficiency promotion” is regulated under the “feed safety legislation” rather than “pharmaceutical legislation” in Japan.  Some antiseptics (AS) and an antiprotozoal (AP-Pr) are not within the remit of VMP authority in Australia.  Chemicals used in animal barn and/or fish preserve may be regulated under “environmental legislation” in some countries. Currently outside the reach of VICH

Part 2 Guidelines in Place

ItemTitle Product Category Type of document #1 Guidance on pharmaceutical fixed combination products (EMEA/CVMP/83804/05) General Technical requirement guideline #2 Questions and answers on the CVMP guideline on fixed combination products (EMEA/CVMP/83804/2005) APAdditional document to #1 #3 European Legislation (EU Directive 2001/82/EC ), (p16)Art 13b GeneralLegal basis for #1 and #2 #4 CVM GFI #24 Drug Combinations for Use in Animals GeneralTechnical requirement guideline #5 WAAVP guideline: Anthelmintic combination products targeting nematode infections of ruminants and horses AP Technical requirement guideline #6 Australian Pesticide and Veterinary Medicine Agency: Preamble for WAAVP guideline: Combination anthelmintic products for ruminants and horses AP Statement adopting #5 WAAVP GL as National GL Guidelines/Guidance in Place

Item TitleCategoryScope #1 Guidance on pharmaceutical fixed combination products General EU data requirements for efficacy, safety and residues documentation for veterinary medicinal products, containing 2 or more active substances. #4 CVM GFI #24 Drug Combinations for Use in Animals General Information and data to demonstrate that the combination of drugs provides a benefit that cannot be obtained by the use of each of the drugs individually #5 WAAVP guideline: Anthelmintic combination products targeting nematode infections of ruminants and horses AP A scientific basis for the approval Anthelmintic products with two or more constituents with similar spectra of activity from different pharmacological classes For use in addition to the existing requirements/GLs for single-API products. Technical Requirement GLs in Place

Parts#1: EMEA/CVMP/83804/05#4: FDA/ CVM GFI #24 Introductory part  Introduction (background)  Scope  Legal Basis  Introductory statement Discussion part  Justification of the Combination  Interactions  Indications  Potential Advantages Improvement of activity Broadening of the activity spectrum Use of a combination product versus combined use of single substances  Risk-Benefit assessment  Non-Interference  Rational  Titration  Ranges  General Efficacy  Combination Claims and Treatment Comparisons (very in detail) Dossiers Requirements part  General requirements  New fixed combination products  Combination products that meet the criteria for well established use  Combination products that meet the criteria for generic application  Specific Requirements  Safety and residues documentation  Preclinical and clinical documentation (Preclinical data, Dose-finding, Tolerance, Clinical data, Resistance, Exceptions) Structure –General GLs-

Parts#5: WAAVP/Australia Introductory part  Introduction (general)  Combining anthelmintics: current situation  Objectives of the anthelmintic combination guideline Discussion part  Rationales for the use of anthelmintic combination products Managing existing resistance Delaying anthelmintic resistance Specific targeting of dose-limiting species Maximizing breadth of spectrum  Concerns about fixed-dose anthelmintic combination products Drug–drug interactions Common mechanisms of resistance Best-practice management of combination anthelmintics Dossiers Requirements part  Justification for the combination  Dose determination data on the anthelmintic constituent actives in the combination  Target animal safety and pharmacokinetic data showing non- interference and acceptable safety  Product bioequivalence  Dose confirmation studies  Field efficacy studies Structure –AP GL –

Conclusion  General combination GL  EU(#1) and US(#4) are the representative General GLs.  Internationally harmonized GL by extracting appropriate elements from them.  Specific combination GL  Main target : Anti-Parasitics  Drug resistance control will be a main objective.  Inclusion of WAAVP(#5)GL into VICH framework should be explored in collaboration with the Anthelmintics-EWG.  Other specific combination may be a target in the future.  After some experiences  Further discussion by the VOF and SC members needed

Mission Completed Thank you 感謝