Albuquerque Journal

Drugmakers pledge no shortcuts on covid vaccine

Effort is to ‘help ensure public confidence in the ... process’

- BY NAOMI KRESGE BLOOMBERG

Drugmakers racing to produce Covid-19 vaccines pledged to avoid shortcuts on science as they face pressure to rush a shot to market.

In an unusual public letter, the companies agreed to submit the vaccines for clearance only when they’re shown to be safe and effective in large clinical studies. The chief executive officers of nine frontrunne­rs in the push for a coronaviru­s inoculatio­n signed the pledge: AstraZenec­a, BioNTech, GlaxoSmith­Kline, Johnson & Johnson, Merck, Moderna, Novavax, Pfizer and Sanofi.

“In the interest of public health, we pledge to always make the safety and well-being of vaccinated individual­s our top priority,” the executives wrote.

The document is intended to counter perception­s that political pressure to deliver a shot as soon as possible may compromise its safety. U.S. President Donald Trump has said a vaccine could be ready before the presidenti­al election in November, and has accused the Food and Drug Administra­tion of slowing its work to hurt him politicall­y.

Public trust in a vaccine will be crucial as public health authoritie­s try to convince millions of healthy people around the world to take it. The pledge also included a promise that companies would work to ensure there are vaccine options “suitable for global access.”

“We believe this pledge will help ensure public confidence in the rigorous scientific and regulatory process by which Covid-19 vaccines are evaluated and may ultimately be approved,” the CEOs said in the letter.

Drugmakers have condensed the developmen­t timeline for their vaccines -- normally a matter of years -- down to months, with early results from some of the frontrunne­rs expected before the end of the year. Pfizer has said it could have crucial test readings by October.

The companies said they would meet FDA expectatio­ns for studies with participan­ts across diverse population­s. Moderna recently slowed the enrollment of its trial, resulting in a delay of about a week, in order to recruit more people from minority communitie­s at high risk from the virus, CNBC has reported.

Any data that form the basis of an emergency-use authorizat­ion for a vaccine should be made public, Merck CEO Ken Frazier said last week. “The scientific community can actually pore through that data and assure the public that it has been looked at objectivel­y,” Frazier said at a meeting of pharma manufactur­ers.

The pledge did not include China’s Sinovac Biotech or CanSino Biologics. Russia and China have already started using experiment­al vaccines on a limited basis before tests in humans were complete.

 ?? HANS PENNINK/ASSOCIATED PRESS ?? Nurse Kathe Olmstead, right, gives volunteer Melissa Harting, of Harpersvil­le, N.Y., an injection as the world’s biggest study of a possible COVID-19 vaccine, developed by the National Institutes of Health and Moderna Inc., gets underway during July in Binghamton, N.Y.
HANS PENNINK/ASSOCIATED PRESS Nurse Kathe Olmstead, right, gives volunteer Melissa Harting, of Harpersvil­le, N.Y., an injection as the world’s biggest study of a possible COVID-19 vaccine, developed by the National Institutes of Health and Moderna Inc., gets underway during July in Binghamton, N.Y.

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