Editor's note

Whether you’re someone who takes the odd ibuprofen for an occasional headache, or you have a chronic condition requiring regular medication, you can be reasonably confident the drug you’re using will benefit the condition it’s intended for. And it will be safe, if taken as instructed. You can be confident of this because it took years of animal and human studies to prove both the medication’s safety and effectiveness.

Today, we explain the four phases of human trials a drug has to go through before it gets to market, and how the gold standard of drug testing - the randomised controlled trial - actually works. And we have a handy animation to make the concepts easier to digest.

Sasha Petrova

Deputy Editor, Health + Medicine

Top story

A drug needs to pass quite a few hurdles before it gets to the market. The Conversation/Wes Mountain

Explainer: how do drugs get from the point of discovery to the pharmacy shelf?

Sabine Braat, University of Melbourne; Elaine Mary Pascoe, The University of Queensland; Katherine J Lee, Murdoch Childrens Research Institute; Laurent Billot, UNSW

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.

Health + Medicine

  • Randomised control trials: what makes them the gold standard in medical research?

    Katherine J Lee, Murdoch Childrens Research Institute; Elaine Mary Pascoe, The University of Queensland; Laurent Billot, UNSW; Sabine Braat, University of Melbourne

    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.

  • How to talk to your child about suicide

    Rachael Sharman, University of the Sunshine Coast

    If a child is old enough to ask about suicide, then they're probably old enough for a discussion about it.

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