Completed Infection & Immunity Lungs & Breathing

Two-month Regimens Using Novel Combinations to Augment Treatment Effectiveness for drug-sensitive Tuberculosis: the "TRUNCATE-TB" trial

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AI plain-English summary

Tuberculosis patients in countries with overstretched healthcare systems could soon receive just two months of treatment instead of the standard six. The TRUNCATE-TB trial will test whether four novel two-month drug combinations can cure drug-sensitive TB with acceptably low relapse rates, then retreat the small number of patients who do relapse. Current six-month regimens strain already underfunded TB programmes, and long treatment times fuel the emergence of drug-resistant TB. If the shorter regimens work, TB clinics could treat far more patients with the same resources, reduce the pressure that breeds multi-drug-resistant TB, and cut costs. The trial will recruit 1,300 patients across 12 Asian treatment centres, follow them for two years, and compare clinical outcomes, side effects, quality of life, and healthcare costs against the standard six-month course. Success would transform how TB programmes operate globally—not by inventing new tools, but by using existing drugs more efficiently in a strategy that matches real-world resource constraints.

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TB incidence rates are falling only very slowly in many high burden countries that have healthcare systems for TB that are overstretched and experiencing large funding gaps. Current tools and systems are clearly not able to solve the problem in the near future and alternatives must be explored - as a matter of urgency - that allow healthcare systems to use resources more effectively and economically to treat and cure more patients with drug-sensitive disease. Multi-drug-resistant (MDR)-TB is also an increasing problem, and a further advantage of improving treatment for drug-sensitive TB may be that it reduces the drive towards generating new cases of MDR-TB. We propose a new strategic approach: instead of the current standard of care of 6 months treatment for drug-sensitive TB, we propose an approach that focuses resources on optimizing individual treatment for just 2 months, then stopping and following patients in order to re-treat the small proportion of those who relapse subsequently (which is expected to be with drug-sensitive organisms). In addition to saving programme resources, stopping after 2 months may reduce the drug pressure for generating MDR-TB as patients not taking medication cannot breed drug resistance. If relapse rates are relatively low, it is possible that such a strategy could be highly cost effective. With recent advances in TB drug development, it is now likely that we can find one or more 2-month combination regimens with low rate of relapse that can be used in such a strategy. Previous trials show that, even with standard drugs, rates of relapse with shorter course TB treatment are low (usually below 10%). With the new drugs that have new mechanisms of action, it is likely that 2-month treatment combinations can be constructed that will have very low rates of relapse - this has already been shown in a mouse model of TB. The only way to test which of the many promising regimens may achieve good cure rate of TB with just 2 months of treatment is to do human trials in which treatment is stopped at this time point and patients are followed for relapse. The Two-month Regimens Using Novel Combinations to Augment Treatment Effectiveness for drug-sensitive TB (TRUNCATE TB) trial is a randomized open label, multi-arm multi-stage, parallel group trial in which we will compare four novel strategies - each using a different initial 2 month treatment combination including one or more novel drugs, and a subsequent 6-month retreatment course with standard drugs for those who relapse - against a 6 month treatment course with standard drugs from the outset. TRUNCATE TB will recruit 1300 patients with confirmed drug-sensitive pulmonary TB and allocate them at random to receive one of the novel 2 month treatment combinations or 6 months standard-of-care treatment. All patients will be followed for 2 years to detect exacerbation of symptoms and be evaluated for relapse. Information on clinical outcomes, microbiological clearance of TB, adverse events, quality of life and healthcare utilisation and costs will be collected. Treatments will be compared for their overall outcome (what proportion of people still have TB in their sputum at 2 years after study entry). If the strategies are equivalent on this outcome then the various advantages and disadvantages of the strategies can be compared including safety, patient acceptability and quality of life, resource use and costs, and drug resistance. We will also look for markers of response that could permit refinements of the strategy (e.g. by identifing groups of patients, if any, in whom 2 months' treatment can be reliably predicted to be inadequate). The trial will be conducted at approximately 12 large TB treatment centres within an Asian TB trials network. This trial addresses a question of high relevance to real-world TB programme settings. It has the potential to transform the way TB programmes operate and to have a major impact on global health.

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Researchers

Andrew Nunn (Co-Investigator)Angela Crook (Principal Investigator)Chester Drum (Co-Investigator)Erlina Burhan (Co-Investigator)Hong Gao (Co-Investigator)Ibrahim Abubakar (Co-Investigator)Joanne Yoong (Co-Investigator)Jubert Benedicto (Co-Investigator)Lawrence Lee (Co-Investigator)Liang Li (Co-Investigator)Mahesh Parmar (Co-Investigator)Nicholas Paton (Co-Investigator)Patrick Phillips (Principal Investigator)Richard Coker (Co-Investigator)Rovina Ruslami (Co-Investigator)Sabai Phyu (Co-Investigator)Soumya Swaminathan (Co-Investigator)Timothy McHugh (Co-Investigator)Vincent Balanag (Co-Investigator)Yin Bun Cheung (Co-Investigator)

Related Research

Grants with similar aims, by meaning.

Two-month Regimens using novel Combinations to Augment Treatment effectiveness for drug-sensitive Tuberculosis: the "TRUNCATE-TB" trial.
Determining the persister populations in sputum during tuberculosis therapy. A supplementary study to the RIFASHORT trial.
An open-label, multi-centre, randomised controlled trial evaluating the effects of short-course rifapentine-based regimens and additional adherence support on LTBI treatment adherence and completion among adults in the UK
MICA: randomized trial of therapy shortening for minimal TB with new WHO-recommended doses and FDC drugs in African/Indian HIV+/HIV- children
PRecision biomArker Guided MAnagement of TuberculosIs Contacts (PRAGMATIC)

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Research Grant

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