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Hu Yuanqiong China Access to Medicines Research Group OSF Seminar Bangkok; 2011.12.13 Access to Medicines and IPR Advocacy in China -- Review and initial.

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Presentation on theme: "Hu Yuanqiong China Access to Medicines Research Group OSF Seminar Bangkok; 2011.12.13 Access to Medicines and IPR Advocacy in China -- Review and initial."— Presentation transcript:

1 Hu Yuanqiong China Access to Medicines Research Group OSF Seminar Bangkok; 2011.12.13 Access to Medicines and IPR Advocacy in China -- Review and initial SWOT discussion

2 Context  International ◦ MSF launched campaign in 1999 ◦ Major players: WHO, Clinton Foundation, TWN, HAI, ITPC… ◦ Local groups in developing countries: South Africa, Brazil, India, Thailand… ◦ Spotlight: ARV  National ◦ 2003, Chinese government launched national ARV treatment program, first revealed access issues ◦ Major players: INGOs, UN Agencies, local PHA groups ◦ Spotlight: ARV ( 3TC, TDF, EFV, LPV… )

3  National law in nutshell ◦ Patent law  Started product patent on medicine from 1992  WTO accession in 2001, no transition time to implement TRIPS  Flexibilities in law: CL, government use, Bolar exception, parallel import…  Patentability: combination, formulation, new form, new use  Opposition/Invalidation: rare between MNC and generic ◦ Drug regulatory  Proxy exclusive rights: administrative protection…  Data exclusivity: 6 years, not in force  Linkage: non-infringement claim, start changing in practice  Fast track registration: ARVs, national emergency

4 Evaluation Goal: what? Subject: who is advocating? Target: advocate to whom? Content: what?Approach: how? Justification: why? Locating advocacy

5 Lamivudine: 1990 process patent, no product patent thick layers of proxy exclusive protection HIV formulation no marketing GSK donation to gov Supply unstable 2007 process patent due, GSK warning 2009 generic registered, no production 2010 generic invalidation won, 4 months margin TDF: 2006, more than 5000 Chinese PHA opposition 2007 , TDF and pre-drug patented in China 2006 , Brazilian and Indian PHA opposition 2008 and 2009,TDF patent rejected in Brazil and India Others…… All second line ARV patented Intermediate and API patented? What’s wrong and how to change?

6  Sustainable access to affordable, reliable, stable supplied essential medicines  Prioritize health in public policies and laws  Scope of advocacy determined by objective and expertise: ARV

7 Who is advocating?  International in China: ◦ MSF CAME ◦ Oxfam * ◦ TWN ◦ WHO ◦ Clinton Foundation ◦ UNAIDS ◦ UNDP ◦ UN Theme group – Sub- working group ◦ DFID *  National: ◦ ITPC-China ◦ AIDS Care China ◦ Ark of Love ◦ Mangrove ◦ Aizhixing ◦ Yirenping ◦ China Global Fund Watch Initiative ◦ Shanghai Beautiful Life ◦ China Access to Medicines Research Group ◦ Grass roots PHA groups…

8  Maximizing patent flexibility in law ◦ Expanding CL grounds ◦ Balancing protection on patent holder and licensee  Utilizing patent flexibility for public health ◦ ARV as potential breakthrough ◦ Feasibility of CL and non-commercial use ◦ Patentability discussion – which is suitable?

9  Target: Government – MOH, MofCom, SIPO, SFDA  Approaches: ◦ Law review, comments ◦ Civil motion to NPC ◦ Ally with academic & gov think tank  Examples: ◦ CL motion ◦ Patent law, CL rules revision comments ◦ MOH submission  Target: MNC  Approaches: ◦ Price Negotiation ◦ Patent opposition ◦ Boycott campaign  Examples: ◦ EFV negotiation with Merk (ACA) ◦ TDF opposition ◦ 2007 Abbott boycott  Crosscutting approaches: ◦ Seminar, workshop (international, national) ◦ Research (joint), translation, information sharing, publication ◦ Network building and maintaining

10  Raising issue? ◦ Gov increased use of language (CL, public interest…) ◦ Gov – NGO intercourse in law making started shifting ◦ Informal intellectual network set, incl. media ally ◦ Law and policy progress in paper  Setting agenda? ◦ Drug based, issue based ◦ Face-to-face lobby based ◦ Opportunistic, individual  Actual change? ◦ No actual breakthrough in using flexibility  Sensitive to external change? ◦ Little done on new phenomena of FTA, ACTA, IMPACT… ◦ Little done on innovation discussion  All stakeholders engagement? ◦ not enough strategic engagement with generic companies

11 S trength: - Existing intellectual network - Experiences with ARV advocacy - Potential technical allies with patent practitioners - Right political will in SIPO and SFDA - Developing civil society culture - Regional and international NGO network W eakness: - Local knowledge building and research - Transparent and collaborative NGO culture in making - Civil society and capacity in developing - MOH not on board - Local linking to regional & international - Restricted to ARV - Public engagement low O pportunities: -Health reform - Global Fund phase out ? - Continued IP network engagement - Evolving civil society - Power of new media - Increasing local industry awareness - Positive research ally and advocate T hreats: - Corruption and non-transparent policy making - Access to information and data - Freedom of speech and assembly - Overwhelmed pro-WTO/IP phenomena - NGO policy in general - Global financial crisis

12 Thanks!


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