A lifeline to treatment: the role of Indian generic manufacturers in supplying antiretroviral medicines to developing countries
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- Waning, B., Diedrichsen, E. & Moon, S. JIAS (2010) 13: 35. doi:10.1186/1758-2652-13-35
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Indian manufacturers of generic antiretroviral (ARV) medicines facilitated the rapid scale up of HIV/AIDS treatment in developing countries though provision of low-priced, quality-assured medicines. The legal framework in India that facilitated such production, however, is changing with implementation of the World Trade Organization Agreement on Trade-Related Aspects of Intellectual Property Rights, and intellectual property measures being discussed in regional and bilateral free trade agreement negotiations. Reliable quantitative estimates of the Indian role in generic global ARV supply are needed to understand potential impacts of such measures on HIV/AIDS treatment in developing countries.
We utilized transactional data containing 17,646 donor-funded purchases of ARV tablets made by 115 low- and middle-income countries from 2003 to 2008 to measure market share, purchase trends and prices of Indian-produced generic ARVs compared with those of non-Indian generic and brand ARVs.
Indian generic manufacturers dominate the ARV market, accounting for more than 80% of annual purchase volumes. Among paediatric ARV and adult nucleoside and non-nucleoside reverse transcriptase inhibitor markets, Indian-produced generics accounted for 91% and 89% of 2008 global purchase volumes, respectively. From 2003 to 2008, the number of Indian generic manufactures supplying ARVs increased from four to 10 while the number of Indian-manufactured generic products increased from 14 to 53. Ninety-six of 100 countries purchased Indian generic ARVs in 2008, including high HIV-burden sub-Saharan African countries. Indian-produced generic ARVs used in first-line regimens were consistently and considerably less expensive than non-Indian generic and innovator ARVs. Key ARVs newly recommended by the World Health Organization are three to four times more expensive than older regimens.
Indian generic producers supply the majority of ARVs in developing countries. Future scale up using newly recommended ARVs will likely be hampered until Indian generic producers can provide the dramatic price reductions and improved formulations observed in the past. Rather than agreeing to inappropriate intellectual property obligations through free trade agreements, India and its trade partners - plus international organizations, donors, civil society and pharmaceutical manufacturers - should ensure that there is sufficient policy space for Indian pharmaceutical manufacturers to continue their central role in supplying developing countries with low-priced, quality-assured generic medicines.
India has emerged as a world leader in generic pharmaceuticals production, supplying 20% of the global market for generic medicines . The emergence of generic sources supplying quality antiretroviral (ARV) medicines at prices much lower than originator prices undoubtedly accelerated the global scale up of HIV/AIDS treatment. From 2002 to 2008, more than 4 million people were started on antiretroviral therapy (ART) in developing countries .
To date, the vast majority of people in low- and middle-income countries have been treated with generic ARVs produced by Indian manufacturers unhampered by patent and other intellectual property restrictions . This absence of intellectual property barriers also resulted in the development of improved ARV formulations, such as paediatric dosage forms and fixed-dose combination (FDC) ARVs whereby two or more ARVs are combined into one tablet. As of the end of 2009, the United States Food and Drug Administration and the World Health Organization (WHO) Prequalification Programme approved or pre-qualified 57 adult FDCs and 31 paediatric ARV tablets produced by Indian generic manufacturers but only eight adult FDCs and 14 paediatric ARV tablets produced by non-Indian and originator manufacturers [4–6].
The intellectual property framework that positioned India as the "pharmacy of the developing world", however, is rapidly changing. In 2005, India was obliged to amend its patent law to allow product patents on medicines to comply with the World Trade Organization (WTO) Agreement on Trade Related Aspects of Intellectual Property Rights (TRIPS). The introduction of product patents in India is severely constraining generic competition and supply, particularly for newer medicines. Now, there is a threat that the limited policy space that remains will be further constricted by bilateral or regional free trade agreements. Unfortunately, many free trade agreements that have been concluded or are being negotiated between industrialized and developing countries contain measures that restrict access to medicines .
Agreements involving India are of particular concern because of the country's role as a worldwide supplier of low-priced generic medicines. For example, current free trade agreement negotiations between the European Union and India [8, 9] include measures that delay or restrict competition from generic medicines, including: patent term extensions beyond the 20 years required by TRIPS; data exclusivity (that could delay the registration of generic medicines); and border enforcement measures that could block international trade in generic medicines when they are suspected of infringing patents in the countries through which they transit. These types of border measures blocked medicines from reaching patients in Africa and Latin America in 2008 and 2009 when European customs authorities seized Indian-produced generics transiting via Amsterdam airport on suspicion that they infringed Dutch patents . All of these measures can delay or restrict competition from generic medicines and are in direct conflict with the 2001 WTO Doha Declaration on TRIPS and Public Health, and medical ethics [8, 9].
A better understanding of the role that Indian generic medicines producers play in HIV/AIDS treatment in developing countries will shed light on the potential consequences of recently proposed intellectual property measures for global public health. While their relative importance is widely recognized, reliable quantitative estimates of generic ARVs supplied by Indian producers are not available. The purpose of this paper is to quantify the extent to which Indian pharmaceutical manufacturers have contributed to HIV/AIDS treatment in developing countries to better understand the potential implications of current and future policies that may hamper or restrict market entry of generic ARV manufacturers and generic competition.
Market share by volume is calculated in person-years for Indian generic, non-Indian generic and brand ARVs using WHO-recommended adult doses for persons weighing more than 60 kilogrammes (kg) [18, 19]. We provided estimates of producer market share for all ARVs, but also calculated market share among three ARV market niches: paediatric ARVs (all classes), adult nucleoside reverse transcriptase inhibitors (NRTIs) and non-nucleoside reverse transcriptase inhibitors (NNRTIs), and adult protease inhibitors (PIs).
We compared purchase trends for Indian generic, non-Indian generic and brand ARVs, summarizing the number of manufacturers, products/dosage forms, purchases, purchasing countries and value (in US dollars).
We calculated 2008 antiretroviral regimen prices for the most commonly used first-line regimens recommended by the WHO in its 2003 and 2006 treatment guidelines for adults weighing more than 60 kg [18, 19]. We expressed regimen prices as price per person per year. Because most ARV price distributions were skewed dramatically by a few high price outliers, we presented regimen prices using median and quartile prices to accurately convey central tendencies. We differentiate regimen composition by using a "+" when multiple tablets are used to create a regimen (e.g., 3TC+NVP+TDF) and a "/" for FDC formulations (e.g., 3TC/NVP/d4T). We plotted 2003-2008 trends in generic ARV regimen prices along with those of innovator ARV regimens offered through differential or tiered prices, as reported to Médecins Sans Frontières (MSF) in its "Untangling the web of ARV price reductions" . We obtained all ARV prices in United States dollars and adjusted them to the January-December 2008 period using the annual US Consumer Price Index .
Purchase trends for Indian generic, non-Indian generic and originator ARVs, 2003-2008
# Countries reporting any ARV purchase
Indian generic ARVs
# products/dosage forms
# purchasing countries
value (USD millions)
Non-Indian generic ARVs
# products/dosage forms
# purchasing countries
value (USD millions)
# products/dosage forms
# purchasing countries
value (USD millions)
Summary of Indian-produced generic ARVs for countries with highest 2008 purchase volumes
Purchase volume rank
% of ARV volume supplied by Indian generic producers
Value of Indian- produced generic ARV purchases (USD million)
# Indian-produced generic ARV dosage forms purchased
United Republic of Tanzania
Democratic Republic of the Congo
First-line ARV regimen prices comparisons, 2008
Indian generic median price
Non-Indian generic median price
Innovator actual median price
Innovator survey price**
Cat 1, Cat 2
First-line regimens from 2003 WHO guidelines:
New first-line regimens from 2009 WHO guidelines:
These analyses quantify and confirm the exceptional role that India has played in providing quality ARVs at low prices to people with HIV/AIDS in developing countries. More than 80% of all donor-funded ARVs purchased since 2006 were supplied by Indian generic manufacturers. Price reductions noted for commonly used historical first-line regimens were a result of robust generic competition among Indian manufacturers in an environment largely void of intellectual property barriers [23, 24]. Countries across sub-Saharan Africa with high HIV/AIDS burdens, as well as India, are heavily reliant on the availability of Indian-produced generic ARVs to support their national treatment programmes.
Trade-related and intellectual property-related threats to the supply of generic medicines from India are coming at a time when the prospects of ART scale up are already cloudy. New WHO guidelines recommending early initiation of ART  will result in increased numbers of people in need of treatment. At the same time, countries are trying to adopt the new ARV regimens recently recommended by WHO [19, 25]. These newer ARVs offer better side-effect and tolerability profiles, but some of the key ARVs are more widely patented and are much more expensive than regimens used in the past. These WHO changes are welcome and help eliminate historical inequities whereby people in resource-poor countries receive a different standard of care than those in rich countries. However, country budgets within the Global Fund to Fight AIDS, Tuberculosis, and Malaria have been cut , while pledges and contributions appear flat, raising concerns that funds will not be available in-country to adopt the new WHO recommendations [19, 22, 25].
Our study captures only donor-funded purchases and not those made by government-funded HIV/AIDS treatment programmes through such countries as Brazil, South Africa and Thailand. Similarly, we had no access to comprehensive and reliable data on patents and other intellectual property barriers and were, therefore, unable to quantitatively examine these issues in our study. While we systematically cleaned and validated all transactional data, we cannot be confident that we have identified all reporting errors in publicly available data. Prices are inconsistently reported to the Global Fund and the WHO Global Price Reporting Mechanism. Whereas some organizations, such as UNITAID and the Supply Chain Management System arm of the United States President's Emergency Plan for AIDS Relief, provide prices for drug costs only, Global Fund-supported countries often report prices that include not only drug costs, but also add-on costs, such as transport, insurance and taxes.
We attribute ARV price reduction primarily to generic competition, but we note that these price decreases were also spurred through the efforts of HIV/AIDS activists, civil society organizations, national governments, foundations and other international organizations.
Despite these limitations, our research provides valuable quantitative information demonstrating the critical role that Indian generic pharmaceutical manufacturers play in the global treatment of HIV/AIDS in developing countries. These results can and should be used in ongoing and future discussions around intellectual property and access to medicines.
Free trade agreements that may create new intellectual property obligations for India can increase ARV prices, impede the development of acceptable dosage forms, and delay access to newer and better ARVs. Such measures can undermine the international goal to achieve universal access to HIV/AIDS interventions and the 2001 WTO Doha Declaration on TRIPS and Public Health . Rather than agreeing to inappropriate intellectual property obligations, India and its trade partners - along with international organizations, donors, national governments, civil society and pharmaceutical manufacturers - should ensure that there is sufficient policy space for the Indian generic industry to continue its central role in supplying developing countries with low-cost, quality-assured generic medicines.
This research was financed by the United Kingdom Department for International Development. The authors thank Jenny Hochstadt for data management support, and Kajal Bhardwaj, Benjamin Coriat, Leena Menghaney and Ellen 't Hoen for comments provided on earlier versions of the manuscript.
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