Just weeks after the WTO agreed to waive COVID-19 vaccine intellectual property protections, governments, vaccine manufacturers, and vaccination sites worldwide report throwing away millions of doses due to oversupply.
In a nutshell: “We don’t have a capacity issue around the planet,” Moderna CEO Stephane Bancel says in The Wall Street Journal. “It was true two years ago, it’s not true today.” Moderna needs to discard 30 million doses after failing to find takers.
Why the oversupply? Drugmakers produced 13.9 billion doses so far, and efforts like COVAX distributed doses to lower-income countries. According to UNICEF, COVAX ensured “there’s now enough supply of COVID-19 vaccines to reach global demand.”
Worldwide, more than 5.26 billion people have received at least one dose of a COVID-19 vaccine—68.5% of the population, The New York Times says. Many who are not vaccinated don’t want to be, The Wall Street Journal notes.
We don’t need a WTO TRIPS waiver now. We never did. “The agreement announced by the WTO will do nothing to increase COVID vaccination rates in the developing world, while at the same time setting a harmful precedent for the world’s ability to respond to the next pandemic” by weakening IP protections that drive innovation, says BIO President and CEO Dr. Michelle McMurry-Heath.
In fact, we can increase access to drugs around the world AND maintain IP. The Medicines Patent Pool (MPP) has been helping lower income countries access medicine while protecting IP since 2010, and they work with WHO and the NIH to share COVID-19 biotech, including Merck’s molnupiravir and Pfizer’s oral COVID-19 treatment through voluntary licensing agreements.
Currently, therapeutics IP is still protected—and the vaccine experience shows it should stay that way.
More Health Care News:
HHS: Administration secures 3.2 million doses of Novavax COVID-19 vaccine
“The protein-based, adjuvanted vaccine will be made available for free to states, jurisdictions, federal pharmacy partners, and federally qualified health centers if it receives U.S. Food and Drug Administration (FDA) Emergency Use Authorization (EUA), and recommendation from the Centers for Disease Control and Prevention (CDC).”