AbbVie and the Medicines Patent Pool have negotiated a royalty-free licensing and sublicensing agreement on a priority hepatitis C direct acting antiviral, glecaprevir and pibrentasvir (G/P).  This G/P combo is recommended by the WHO as a pan-genotypic adult first-line regimen with ongoing Phase 3 trials for adolescents and children.  G/P has a high resistance barrier and the shortest treatment duration of any HCV regimen to date.

The main drawback of the MPP-AbbVie license is its limited geographic scope – particularly its exclusion of India, a high burden country with a significant population of people living with HCV.  Not only are there fewer countries and territories included in the license (95 and 4 respectively, Table 1) than in previous licenses for direct acting antivirals (DAAs) for HCV, but the percentage of the global population living with HCV covered –  47.5% – is lower than Gilead’s bilateral license for sofosbuvir (105 territories, 62.3% coverage) and BMS’s license for daclatasvir (112 territories, 54.3% coverage).  Consistent with previous licenses, AbbVie has prioritized exclusion of so-called “emerging markets” and upper-middle-income markets, in order to maximize profit in those markets.

This will have grave health consequences now for people suffering with untreated HCV in those countries, and in the future.  Excluding countries with more capacity to finance reasonably priced HCV elimination strategies shrinks the overall market for generic G/P, reduces economies-of-scale for generic producers, and thus undermines treatment and elimination strategies in licensed territories as well.  As another negative, the license restricts production to companies located within the licensed geographies plus India (as a manufacturing country only).

The patent situation in India and other excluded territories is important.  There are five relevant patents filed on G, P, and G/P in India, one of which involving pibrentasvir is being opposed by I-MAK and Third World Network.  A first examination report on that application, since amended, detailed multiple grounds for denying a patent. If oppositions are expanded to the other four applications, if they are all successful, and if AbbVie does not unduly extend evaluation of its patent applications via substitutions, selection, amended or protracted appeals, then Indian generic companies would eventually be permitted to supply India and other excluded territories where no granted patent is in force.  Thus, the MPP licenses accomplish some “wholesale” work in facilitating generic entry and competition in 99 countries and territories.  Moreover, complementary oppositions could eventually open up opportunities in some excluded territories as well, since the license allows supply to countries and territories if no granted patent will be infringed.  Unfortunately, G/P appears to be very widely patented in LMICs, with 30 out of 32 extra-territorial LMICs in the MedsPAL database reporting granted and pending patents (Table 2). http://www.medspal.org/?product_standardized_name=Glecaprevir/Pibrentasvir%20100/40%20mg. On the plus side, there is some possibility that the MPP, countries, and activists will be able to convince AbbVie to expand the licensed territory, including in India, while generic licensees develop and register the licensed product.  AbbVie should clearly do so, but even if it does not expand the licensed territory, countries where patents are in effect still have the option to issue compulsory licenses and to be lawfully supplied by generic sublicensees.

No one should have to suffer from untreated HCV—a virus with very good prognosis for cure but where gross inequities are keeping medicines out of reach. Countries should urgently deploy all available mechanisms, including compulsory licensing, in order to obtain low cost, generic versions of G/P.

Table 1:  Countries and Territories Included in the License

Afghanistan  Marshall Islands
 Angola  Mauritania
 Antigua and Barbuda  Mauritius
 Bangladesh  Micronesia
 Belize  Morocco
 Benin  Mozambique
 Bhutan  Myanmar
 Bolivia  Namibia
 Botswana  Nauru
 Burkina Faso  Nepal
 Burundi  Niger
 Cambodia  Nigeria
 Cameroon  Niue
 Cape Verde  Pakistan
 Central African Republic  Palau
 Chad  Papua New Guinea
 Comoros  Philippines
 Congo  Rep.
 Cook Island  Reunion Islands
 Côte d’Ivoire  Rwanda
 Democratic Republic of the Congo  Saba
 Djibouti  Saint Eustatius
 Dominica  Saint Kitts and Nevis
 Egypt  Saint Lucia
 Equatorial Guinea  Saint Vincent & the Grenadines
 Eritrea  Samoa
 Ethiopia  Sao Tome and Principe
 Fiji  Senegal
 Gabon  Seychelles
 Gambia  Sierra Leone
 Georgia  Solomon Islands
 Ghana  Somalia
 Grenada  South Africa
 Guadeloupe  South Sudan
 Guinea  Sri Lanka
 Guinea-Bissau  Suriname
 Guyana  Swaziland
 Haiti  Tanzania
 Indonesia  Timor-Leste
 Jordan  Togo
 Kenya  Tunisia
 Kiribati  Turkmenistan
 Laos  Tuvalu
 Lesotho  Uganda
 Liberia  Vanuatu
 Libya  Vietnam
 Madagascar  West Bank & Gaza
 Malawi  Yemen
 Maldives  Zambia
 Mali  Zimbabwe

Countries in bold have filed or granted patents

 

Table 2:  LMICs with Granted or Pending Patents Excluded from the License

(MedsPAL Nov. 13, 2018)

Albania Macedonia
Armenia Malaysia
Azerbaijan Mexico
Belarus Moldova
Bosnia & Herzegovina Mongolia
Brazil Montenegro
China Paraguay
Colombia Peru
Costa Rica Russia
Dominican Republic Serbia
Ecuador Tajikistan
Guatemala Thailand
India Turkey
Kazakhstan Ukraine
Kyrgyz Republic Venezuela

*Nicaragua and El Salvador listed at having no relevant patent filed