Health Canada is proposing a new system to fast-track urgent drugs for children, the elderly and those with serious or life-threatening conditions. This would rely on decisions made by regulators in other jurisdictions.
Health Canada is proposing to allow some prescription drugs into the country with only 'cursory clinical review.' Here's why we should be worried.
Black mambas are extremely dangerous.
Coordinated international efforts may be key to improving the life expectancy and health of many snakebite victims.
Baroness Tessa Jowell speaking in the House of Lords.
There are several things we can do to speed up the development of new drugs, without putting patients at risk.
How a technology born from finance – the blockchain – can help the pharmaceutical industry to carry out clinical trials that protect patients.
The experimental technique of ‘deep brain stimulation’ has improved the lives of patients with treatment-resistant depression, despite the ‘failure’ of a large clinical trial.
For some patients, drilling a hole in the skull and inserting an electrode into the 'sadness centre' of the brain offers relief from debilitating and otherwise treatment-resistant depression.
Apple's Eyes Studio/Shutterstock.com
We need to ensure cancer research addresses what matters most.
Even if they are not treated, only about three per cent of men will die of prostate cancer over their lifetime, most in their 70s or 80s.
A family physician and public health researcher explains why he isn't getting a prostate cancer test in Movember or at any time in the near future.
A drug needs to pass quite a few hurdles before it gets to the market.
The Conversation/Wes Mountain
Only around 10% of new drugs in development make it onto the market. A drug needs to go through animal trials, and then four phases of human trials to be deemed suitable for use in patients.
Randomisation is the only commonly accepted method of ensuring an unbiased estimate of the treatment effect.
The Conversation/Wes Mountain
A randomised controlled trial is the best way to compare a new treatment with the standard treatment. And randomising trial participants is a core feature of the experiment.
It’s hard to test therapies for rare cancers because there are too few people to study.
Rare cancers are hard to research given the few patients that have each type of cancer, so how can we improve treatment for these patients?
Animals have played a pivotal role in countless life-saving discoveries.
Virtually every medical therapy in use today owes its existence to animal experiments. But we can't assume what works in animals will in humans. And sometimes, the mismatch can be dangerous.
Done well, translational science can save lives.
Systematic reviews are rarely applied to basic research. A new study shows how they could separate good data from bad, saving millions in research dollars and speeding life-saving treatments.
In many trials, patients have been told they're getting the sugar pill. They still got better.
DNA holds the secrets of human existence, and studying rare diseases can reveal some of these facts of life.
Rare diseases may only affect a handful of people but their treatment benefits everyone.
There is evidence many conditions can be treated without drugs or surgery.
In many cases, the most appropriate treatment for a health condition isn't a drug. It could be a recommendation for a dietary change, a specific exercise, or even a phone app.
Scientists hope that stem cells may be able to repair nerves and other cells that support transmission of electrical impulses in the spinal cord.
Claims that stem cell treatments can repair spinal injuries right now are overblown. But it's not for lack of trying, and the science is certainly progressing.
Better technologies should be adopted in sub-Saharan Africa to deal with childhood cancer.
Better technology to diagnose, treat and manage the disease early enough is needed to improve the survival rates of childhood cancer in sub Saharan Africa.
President Barack Obama signs the 21st Century Cures Act on Tuesday, Dec. 13, 2016, in Washington.
Kevin Wolf/AP Images for Parker Foundation
Lowering the threshold for FDA approval and feeding the agency less rigorous information will increase the likelihood of approvals of unsafe or ineffective drugs and devices.
Despite dozens of trials internationally, the evidence on medical cannabis is unconvincing.
NSW is about to embark on the largest and most definitive clinical trial ever of medicinal cannabis for chemotherapy-induced nausea and vomiting.
If only we had a few more recruits.
Trials into the effectiveness of drugs and treatments struggle to recruit enough participants, yet we rely on their results anyway.