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Johnson & Johnson says FDA has approved extended vaccine expiration date

Johnson & Johnson announced Thursday that the Food and Drug Administration (FDA) has authorized an extension of its COVID vaccine's shelf life from three months to 4.5 months.

Why it matters: Amid a slowdown in vaccine uptake, a number of state health officials had been sounding the alarm that hundreds of thousands of single-shot J&J doses could expire this month.


  • Prior to the FDA's extension, J&J's vaccine could be stored at normal refrigeration temps for up to three months. Pfizer and Moderna's two-shot vaccines must be stored in colder temperatures, but can last for up to six months.
  • The extension is based on "data from ongoing stability assessment studies, which have demonstrated that the vaccine is stable at 4.5 months when refrigerated at temperatures of 36 – 46 degrees Fahrenheit (2 – 8 degrees Celsius)," J&J said in a statement.

The FDA did not immediately respond to Axios' request for comment.

What they're saying: "A single-shot vaccine that provides protection and prevents hospitalization and death is an important tool in the global fight against COVID-19," J&J said.

  • "Evidence from our Phase 3 ENSEMBLE study demonstrates the efficacy of our single-shot COVID-19 vaccine, including against viral variants that are highly prevalent. Regardless of race and ethnicity, age, geographic location and comorbidities, these results remain consistent."
  • Vaccine providers should check the J&J website to confirm the vaccine's latest expiration dates, the company added.

The big picture: The authorization comes as COVID vaccine demand declines in the U.S., though it continues to skyrocket abroad.

  • In the U.S., over 10.1 million J&J doses have been delivered but not administered, according to CDC data.
  • President Biden has said he will send 20 million doses of COVID vaccines, including Pfizer, Moderna and J&J, to other countries by the end of June.

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Women's soccer will get major U.S. exposure this weekend

Women's soccer will get major U.S. exposure this weekend, with the NWSL kicking off its seven-week "Fall Series" on CBS and the FA Women's Super League (England) beginning its season on NBCSN.

Why it matters: It's an exciting time for the sport, which has grown from four million players worldwide in 2006 to roughly 30 million today, and is still riding the momentum of the 2019 Women's World Cup.

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FDA authroizes emergency use of Regeneron antibody treatment given to Trump

The Food and Drug Administration announced Saturday evening it has granted emergency use authorization for Regeneron Pharmaceuticals' antibody cocktail given to President Trump to treat his COVID-19 infection last month.

Why it matters: Regeneron's two monoclonal antibodies, casirivimab and imdevimab, are for people who tested positive for the coronavirus and "who are at high risk for progressing to severe COVID-19," including people who are 65 and older, and/or people with certain chronic illnesses, per an FDA statement.

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Your guide to Congress' certification of Biden's win

There's no doubt about the outcome — Congress will ratify Joe Biden's election win and he'll be sworn in on Jan. 20 — but that won't stop today's political theater that may drag late into the night.

  • Here's our guide to watching the certification debate, with input from legislative aides, historians, election experts and Axios' Ursula Perano.
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4 board members of Texas power grid operator ERCOT resign

Four members of Texas' power grid operator resigned from their posts Tuesday after a winter storm led millions of homes to lose power across the state last week, according to a public filing.

Why it matters: Their resignations come days after Texas' public utility commission launched a probe to discover the "factors that combined with the devastating winter weather to disrupt the flow of power," throughout the state.

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