OUR LATEST NEWS

SimpliciTB / PanACEA Annual Meeting 2025 Convenes in Cape Town

Cape Town, South Africa – 3rd to 5th June 2025

A successful and inspiring Annual Meeting of the SimpliciTB and PanACEA II consortium was held in Cape Town earlier this month, bringing together 70 members from across the partnership to review achievements and chart the path forward for PanACEA III.

Originally planned for Uganda, the meeting was relocated to the Protea Hotel, Sea Point, due to unforeseen circumstances. We are deeply grateful to our Ugandan hosts for traveling to Cape Town and for their continued support, and we extend special thanks to our colleagues at TASK for their invaluable assistance in organising the event.

Over the course of the 2.5-day gathering, attendees engaged in a rich programme of presentations and discussions. Dr Michael Makanga, Executive Director of the Global Health EDCTP3 Joint Undertaking, joined us virtually to deliver an insightful presentation. Highlights included updates on the SimpliciTB trial, OptiRiMox developments, and progress in PanACEA’s drug development pipeline. Contributions from site leads, a Community Advisory Board (CAB) member, and updates on community engagement and the Youth Development Programme further enriched the agenda.

The final day focused on collaborative group discussions that explored priorities and strategic planning for the next phase—PanACEA III.

This meeting reaffirmed the consortium’s dedication to advancing tuberculosis research through global collaboration and shared innovation.

 

OptiRiMoxTB – An international pragmatic trial with Optimised dose of Rifampicin and Moxifloxacin for the treatment of drug susceptible pulmonary tuberculosis (TB)

The OptiRiMoxTB clinical trial is part of SimpliciTB programme, which includes an  international clinical trial and supports the development of capacity in the network of African clinical trial sites.  The  grant is funded  by the EDCTP2 Programme (grant number RIA2017S-2012) .

The OptiRiMoxTB trial is being sponsored and led by the team at  Kibong’oto Infectious Disease Hospital, KIDH in Tanzania. Prof.dr. Stella Mpagama is the Principal Investigator and a Senior EDCTP Fellow and honorary member of staff at the University of St Andrews. The KIDH and wider team are  supported and mentored by University of St Andrews,  who are also providing support to Mr Hamu Mlyuka (BPharm) an EDCTP Clinical Research and Product Development Fellow from Muhimbili University of Health and Allied Sciences, Tanzania also working for the trial.  Long established partners, National Institute  for Medical Research Mbeya Medical Research Centre, Mwanza Medical Research Centre, Kilimanjaro Clinical Research Institute and Ifakara Health Institute, Tanzania,  University College London, Radboud University Medical Centre, Netherlands and TB Alliance are also supporting the sites.

The capacity development aspect of the trial aims to allow new TB trial sites so that they can perform therapeutic clinical trials. The new sites are Kamuzu University of Health Sciences KUHeS – Malawi, the Centres de Recherches Médicales de Lambaréné  and the Instituto Nacional de Saúde, Mozambique.

OptiRiMoxTB is an important development that will test an easy to implement shorter regimen that emerges from our programme of research.  It will test whether a 4-month therapy based on Rifampicin (35mg/kg) +/- Moxifloxacin (400mg) is non-inferior to conventional 6-month DS-TB therapy.  It is anticipated the trial will recruit 414 patients.

All 4 trial sites are now recruiting participants, having successfully recruited 50% and are due to complete recruitment in August 2024.  The sites have had many challenges to overcome throughout the clinical trial preparation phase.

If successful the OptiRiMoxTB regimen will allow individuals with-drug susceptible tuberculosis to be treated with well-established antibiotics in just four months, saving time money and reducing the burden on patients with this disease.

 

New Vitalbacteria Website Launches

We’re thrilled to announce the launch of Vitalbacteria, your trusted source for high-quality MBLA (Molecular Bacterial Load Assay) kits. The new website is now live, offering researchers, clinicians, and laboratories an efficient way to access this powerful tool for bacterial load quantification — especially in tuberculosis (TB) diagnostics.

Why MBLA?

The MBLA assay is a molecular diagnostic technique designed to measure the viable bacterial load in clinical samples. Unlike traditional culture methods, MBLA delivers rapid, reliable, and quantitative results, making it an essential component in both clinical research and routine TB monitoring.

At Vitalbacteria, we provide:

  • 🧪 Validated MBLA assay kits ready for research and clinical use
  • 📦 Easy online ordering and secure shipping
  • 📘 Comprehensive product documentation and support

Whether you’re working in infectious disease diagnostics, clinical trials, or microbiological research, MBLA offers the speed and precision needed to advance your work.

Order Now

The MBLA assay kits are available to order today

👉 Place Your Order Now:    https://www.vitalbacteria.com/

Lancet Publication

We are delighted to announce that our paper, resulting from the SimpliciTB Clinical Trial has been published in the lancet – you can read the full text here –  https://www.thelancet.com/journals/laninf/article/PIIS1473-3099%2824%2900223-8/fulltext

Clinical Trial Results Presented at CROI 2023

Clinical Trial for Drug-Sensitive and Drug-Resistant TB Regimen Evaluated Shorter Regimens

A clinician from the SimpliciTB trial in the Philippines preparing treatment for a clinical trial participant in 2019.

A clinician from the SimpliciTB trial in the Philippines preparing treatment for a clinical trial participant in 2019.

 

SEATTLE (February 20, 2023)—Results of TB Alliance’s SimpliciTB clinical trial were presented today at the 30th annual CROI 2023 conference. SimpliciTB was conducted to evaluate the BPaMZ regimen, consisting of bedaquiline (B), pretomanid (Pa), moxifloxacin (M), and pyrazinamide (Z). This combination previously showed high efficacy and treatment shortening potential in both preclinical evaluations and an early-stage clinical study in drug-resistant patients.

SimpliciTB enrolled 455 patients with drug-susceptible (DS) or drug-resistant (DR) tuberculosis (TB) at 26 sites across eight countries: South Africa, Tanzania, Georgia, Brazil, Russia, the Philippines, Uganda, and Malaysia.1 The clinical trial was designed to evaluate the safety and efficacy of BPaMZ in patients with either DS-TB or DR-TB. As presented at CROI, the results of the trial showed that the BPaMZ regimen was highly potent against the TB bacteria, meeting its primary endpoint with DS-TB participants 2.93 times more likely to culture convert by week 8. However, the 4-month experimental BPaMZ regimen did not meet the secondary endpoint of noninferiority in percent favorable outcomes compared to 6 months of HRZE in DS-TB. This was due to adherence challenges, with approximately 10% of patients on the BPaMZ arms discontinuing treatment due to side effects.1

“Innovative clinical trials like SimpliciTB help us better understand how novel drug regimens work against both drug-sensitive and drug-resistant TB, lighting the way to better treatment options for all people with TB,” said Dr. Muge Cevik, infectious diseases clinician and researcher at the University of St. Andrews and presenter of the SimpliciTB trial results at CROI 2023.

In 2021, 10 million people were infected with TB and about 1.6 million people died. It is estimated that about 500,000 people every year are infected by a drug-resistant form of the disease, and in some regions as many as 40% of all cases are drug-resistant.2 Novel drug regimens are urgently needed to help bring the TB pandemic under control.

TB Alliance plans to submit data from SimpliciTB to a peer-reviewed publication – https://www.tballiance.org.za/news/tballiance-simplicitb-results-croi-2023

Professor Stephen Gillespie

Professor Stephen Gillespie spoke at the UNITE4TB Webinar which took place on 8th June.  He summarised the current role of biomarkers in TB treatment and clinical trials. Explaining the concept of microbiological biomarkers, highlighting the current gold standard techniques (liquid and solid mycobacterial culture), and demonstrated the challenges posed. He also gave an overview of the most important TB biomarkers under evaluation.

A link can be found on this page https://www.unite4tb.org/newsroom/unite4tb-webinar-recap-expert-interview-biomarkers-tb-clinical-trials to hear the full webinar recording.

A Webinar for Frontiers in Antibiotics on the subject of “Antibiotic Drug Development- Refilling the Pipeline” was also hosted and convened by Professor Gillespie. Speaking at the Webinar were Dr Derek Sloan and Dr Robert Hammond. Here is the link to the seminar: Refilling the Antibiotic Pipeline – Webinar By Frontiers in Antibiotics https://youtu.be/X-6lP64B7eY 

Professor Gillespie also participated as a board member for the most recent Medical Research Council African Leaders Scheme grant call and was an invited participant in the Wellcome Trust/University of Liverpool Witness Seminar on the “Organisation of Public Health Microbiology”.

 

 

X