Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The Ineos Oxford Institute for antimicrobial research (IOI) has awarded £5 million to a group of 17 interdisciplinary researchers from Oxford University to develop new therapies for drug-resistant tuberculosis.

Tuberculosis (TB) is the oldest and most deadly disease in human history, causing over 1.2 million deaths every year. TB is an infectious airborne disease that mainly affects the lungs. It is caused by the bacterium Mycobacterium tuberculosis (Mtb). 

The main treatment option for TB is long courses of multiple antibiotics. However antimicrobial resistance (AMR) – a process in which bacteria have developed the ability to resist the action of medicines - has made it harder, longer and more costly to treat TB. Half a million people are infected with multidrug-resistant Mtb each year and the need for new treatment options is urgent.

Insufficient investment and innovation in TB drug development has led to a limited number of potential treatments reaching clinical trials.  

To tackle the global health threat caused by TB, the IOI has awarded £5m to support the establishment of an Oxford consortium comprising chemists, biologists, clinicians, vaccinologists and health sociologists who will work collaboratively through 5 interconnected stages from drug discovery and testing to clinical trials and public engagement to develop new therapies for TB.

Please read the full story on the Ineos Oxford Institute website. 

Similar stories

New study confirms malaria drug is safe for children and could reduce disease spread

A major study in The Lancet Infectious Diseases confirms that single low-dose primaquine is safe and effective in reducing malaria transmission in young children. Analysing data from over 6,000 patients, researchers found it effective even in young children and areas with high malaria burden. The findings support expanding primaquine use to tackle drug-resistant malaria in Africa. A child-friendly formulation is urgently needed to maximise its impact on malaria elimination efforts worldwide.