Unexplained Illness In Participant Halts J&J Vaccine Trials

Johnson & Johnson has said that it has temporarily paused its COVID-19 vaccine candidate clinical trials due to an unexplained illness in a study participant, delaying one of the highest profile efforts to contain the global pandemic.

The participant’s illness is being reviewed and evaluated by an independent data and safety monitoring board as well as the company’s clinical and safety physicians, the company said in a statement.

J&J said that such pauses are normal in big trials, which can include tens of thousands of people. It said the “study pause” in giving doses of the vaccine candidate was different from a “regulatory hold” required by health authorities. The current case is a pause.

However, J&J’s move follows a similar one by AstraZeneca Plc. In September, AstraZeneca paused late-stage trials of its experimental coronavirus vaccine, developed with the University of Oxford, due to an unexplained illness in a UK study participant.

While trials in the UK, Brazil, South Africa and India have resumed, the U.S. trial is still on hold pending a regulatory review.

Dr. William Schaffner, a professor of infectious diseases at the Vanderbilt University School of Medicine, said by email that “Everybody is on the alert because of what happened with AstraZeneca,” adding that it could take a week to gather information.

“It would have to be a serious adverse event. If it was something like prostate cancer, uncontrolled diabetes or a heart attack – they wouldn’t stop it for any of those reasons. This is likely to be a neurological event,” he said.

Last month, J&J said its experimental COVID-19 vaccine produced a strong immune response against the novel coronavirus in an early-to-mid stage clinical trial, following which the company kicked off a final 60,000-person trial, whose results had been expected by the end of this year or early 2021.

Johnson & Johnson declined to elaborate about the illness due to privacy concerns. It did say that some participants in studies get placebos, and it was not always clear whether a person suffering a serious adverse event in a clinical trial received a placebo or the treatment.

Stat News reported the pause earlier in the day citing a document sent to outside researchers, which stated that a “pausing rule” had been met, the online system used to enroll patients in the study had been closed and the data and safety monitoring board would be convened.

Recent Posts

  • Featured

PM Modi Is Scared, He May Even Shed Tears On Stage: Rahul Gandhi

On Friday, April 26, Congress leader Rahul Gandhi retaliated against Prime Minister Narendra Modi over his attack on the grand…

10 hours ago
  • Featured

Climate Change Poses Dire Health And Human Rights Risks

Climate change has not traditionally been seen as a health and human rights concern — but that may be changing…

12 hours ago
  • Featured

Tech To Decrease Food Loss & Increase Farmer Incomes

Food loss after harvest has economic implications for the farmer and also impacts the environment due to loss of agricultural…

15 hours ago
  • Featured

E-Bikes Could Cut Smog, Congestion & Energy Use — But Will They?

The global market for e-bikes is surging. These bicycles, usually equipped with pedals and an electric motor assist, are popular…

1 day ago
  • Featured

Difference In Environmental Footprints Between Economic Strata

A new study that analysed consumption data in India found stark differences in the water, particulate matter and carbon footprints…

1 day ago
  • Featured

How Climate Change Is Killing Us, In More Ways Than One

We’ve all heard about climate change’s effect on our planet — but do you know about the many ways it…

3 days ago

This website uses cookies.