Month: January 2018

EB142: KEI statement on WHO’s decision on the Global strategy and plan of action on public health, innovation and intellectual property

Posted on by Thiru

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After lengthy negotiations, on Friday, 26 January 2018 the World Health Organization’s Executive Board approved a decision to reinvigorate the Organization’s work program on innovation and access to medicines. Here are two quotes from KEI on the decision: James Love,…

EB142: KEI statement on Preparation for the third High-level Meeting of the General Assembly on the Prevention and Control of Non-communicable Diseases

Posted on by Thiru

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The World Health Organization’s (WHO) Executive Board is expected to discuss agenda item 3.8 on Preparation for the third High-level Meeting of the General Assembly on the Prevention and Control of Non-communicable Diseases, to be held in 2018 the either…

EB142: KEI statement on the Global Strategy and plan of action on public health, innovation and IP

Posted on by Thiru

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The World Health Organization’s (WHO) Executive Board is expected to discuss agenda item 3.7 on the Global strategy and plan of action on public health, innovation and intellectual property either on Wednesday, 24 January 2018 or Thursday, 25 January 2018.…

EB142: KEI statement on Addressing the global shortage of, and access to, medicines and vaccines

Posted on by Thiru

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On Wednesday, 24 January 2018, the World Health Organization’s (WHO) Executive Board is expected to discuss agenda item 3.6 on Addressing the global shortage of, and access to, medicines  and vaccines. Non-state actors in official relations with the WHO are…

PhRMA letter on Colombia Resolution 5246

Posted on by James Love

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On January 15, 2018, PhRMA provided comments on the Colombian Resolution 5246, a public interest declaration for several drugs for the hepatitis c virus (HCV). A copy of the PhRMA letter is attached below. It is a combination of complaints…

Expert Panel charts a road map for WHO’s engagement on transparency and R&D

Posted on by Thiru

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In November 2017, the World Health Organization (WHO) published a report charting a path forward for the expansion of WHO’s work on the transparency of R&D costs and medicines prices while rekindling the prospects for WHO to assume the mantle of…

NIH wants to give Gilead a new, government subsidized monopoly on CAR T technology, this one for CD-30 proteins.

Posted on by James Love

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We have a briefing note on this license here: 2018: Briefing note on NIH proposed license to Gilead for CD-30 CAR T technology

2018: Briefing note on NIH proposed license to Gilead for CD-30 CAR T technology

Posted on by James Love

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Contact: Kim Treanor 202-332-2670; kim.treanor@keionline.org January 5, 2018 The National Institutes of Health (NIH) has proposed an exclusive license with Gilead for certain patent applications for inventions that target CD-30 proteins and CAR T technologies. The proposed license is to…

Chilean Cámara de Diputados Votes Overwhelmingly To Proceed With Compulsory Licenses for HCV Drugs

Posted on by Andrew Goldman

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The Cámara de Diputados of the Chilean Congress has overwhelmingly passed a resolution calling on the President to advance the compulsory licensing request on HCV drugs made in March 2017 by patients, advocates including Innovarte NGO, and elected officials. The resolution, Number…