{"id":5288,"date":"2023-12-25T21:42:36","date_gmt":"2023-12-25T20:42:36","guid":{"rendered":"https:\/\/www.bioga.org\/?p=5288"},"modified":"2023-12-30T18:02:40","modified_gmt":"2023-12-30T17:02:40","slug":"zendal-and-iavi-receive-funding-to-advance-spanish-tuberculosis-vaccine-efficacy-trial-in-africa","status":"publish","type":"post","link":"https:\/\/www.bioga.org\/en\/zendal-and-iavi-receive-funding-to-advance-spanish-tuberculosis-vaccine-efficacy-trial-in-africa\/","title":{"rendered":"Zendal and IAVI receive funding to advance Spanish tuberculosis vaccine efficacy trial in Africa"},"content":{"rendered":"
TB kills 1.3 million people a year and sickens more than 10 million people annually.\u00a0<\/strong><\/h6>\n
A new TB vaccine is needed to reach the global End TB goals.\u00a0<\/strong><\/h6>\n
MTBVAC is a highly promising vaccine candidate that has the potential to be used as an alternative to BCG vaccination in infants and for prevention of TB disease in adolescents and adults.\u00a0<\/strong><\/h6>\n
Grant from the Bill & Melinda Gates Foundation to IAVI will support efficacy trial.<\/strong><\/h6>\n

NEW YORK, U.S. and O PORRI\u00d1O, SPAIN \u2014 December 18, 2023 \u2014 IAVI, a global nonprofit scientific research organization, and Spanish biopharmaceutical company Biofabri, a subsidiary of Zendal, today announced that the Bill & Melinda Gates Foundation has awarded IAVI US$55 million to conduct a Phase IIb trial assessing the safety and efficacy of the tuberculosis (TB) vaccine candidate MTBVAC to prevent active TB lung disease in adolescents and adults. This funding has been made possible in part through a grant provided by Open Philanthropy, a grant-making organization that aims to use its resources to help others as much as it can. This trial is also supported by additional funding provided by the German Federal Ministry of Education and Research (BMBF) through the KfW Development Bank, which provides funding to IAVI and partners<\/a>\u00a0in support of developing MTBVAC. It is anticipated that the trial will begin enrolling participants in mid-2024.<\/p>\n

\u201cWe\u2019re thrilled to have secured the investment needed to advance this promising vaccine candidate into an efficacy study,\u201d said Mark Feinberg, M.D., Ph.D., president and CEO of IAVI. \u201cThe world urgently needs a new, effective vaccine that can prevent TB disease in adults and adolescents, and we are hopeful that MTBVAC will be part of the solution to finally end the TB epidemic. We are grateful to the Bill & Melinda Gates Foundation for their support of our late-stage development work on MTBVAC and to Open Philanthropy, whose visionary investment could accelerate the availability of MTBVAC by several years, if it is shown to be safe and efficacious in the upcoming efficacy trial.\u201d<\/p>\n

\u201cThis is a historic opportunity to learn whether this promising TB vaccine candidate, MTBVAC, can prevent active TB disease in adolescents and adults, the population among whom most TB disease and transmission occurs,\u201d said Lewis Schrager, M.D., senior leader of TB vaccine development efforts at IAVI. \u201cIf MTBVAC were shown to safely prevent TB disease in this population, this vaccine could prove to be critically important in global strategies to suppress the TB pandemic given its ease of use, low cost, and anticipated widespread availability.\u201d<\/p>\n

Previous Phase Ib\/IIa dose-ranging studies of MTBVAC in adults and neonates demonstrated favorable immunogenicity and safety profiles. In addition to this Phase IIb trial, Biofabri is conducting a Phase III trial of MTBVAC (NCT04975178<\/a>) in neonates in South Africa, Madagascar, and Senegal, with support from the European & Developing Countries Clinical Trials Partnership (EDCTP). Biofabri and the HIV Vaccine Trials Network are planning a Phase IIa trial (NCT0547890<\/a>) evaluating the safety and immunogenicity of MTBVAC in people living with HIV whose viral loads are well controlled on antiretroviral therapy, scheduled to begin in South Africa in mid-January 2024.<\/p>\n

Only a handful of TB vaccine candidate efficacy trials have ever been conducted. This study of MTBVAC to prevent TB disease will be conducted in approximately 4,300 people who have latent TB infection. Participants will be between the ages of 14 and 45, living in South Africa and select other sub-Saharan African countries in areas with high TB burden. Participants at 15-20 trial sites will receive either a single dose of MTBVAC or placebo and be observed for two to three years.<\/p>\n

Kundai Chinyenze, M.D., MPH, IAVI Africa director, said, \u201cWe are gratified to be able to begin working on this efficacy trial in a region of the world where TB is a leading contributor to morbidity and mortality, especially for people living with HIV. IAVI\u2019s long history in conducting clinical trials in Africa and our strong network of regional and global partners provide a solid foundation for the successful conduct of this important trial.\u201d<\/p>\n

MTBVAC, designed by the Spanish researcher Carlos Martin, Ph.D., from the University of Zaragoza, and Brigitte Gicquel, Ph.D., of Institut Pasteur, was in-licensed by Biofabri (Zendal Group). Theonly available TB vaccine,bacille Calmette-Gu\u00e9rin (BCG), is derived from\u00a0Mycobacterium bovis,\u00a0<\/em>a bacterium that causes a TB-like disease in cows.\u00a0<\/em>BCG is largely ineffective in preventing TB in adolescents and adults. MTBVAC is the only live, attenuated vaccine derived from\u00a0Mycobacterium tuberculosi<\/em>s, the bacterium that causes TB disease in humans, in the pipeline. Given its derivation from the human, rather than the bovine, TB-causing organism, MTBVAC has the potential to generate a broad protective immune response against TB. The vaccine is administered as a single dose via intradermal delivery and does not require the use of an adjuvant.<\/p>\n

Esteban Rodriguez, CEO, Biofabri, said, \u201cWe are delighted by the fantastic opportunity \u2014 through the tremendous efforts of IAVI, and the valuable support provided by the Bill & Melinda Gates Foundation, Open Philanthrophy, and the German Federal Ministry of Education and Research (BMBF) through the KfW Development Bank \u2014 to now evaluate the efficacy of MTBVAC in adolescents and adults. The outcome of the efficacy studies in neonates as well as those in adolescents and adults will provide us with a pathway to license MTBVAC for all age groups.\u201d<\/p>\n

Should MTBVAC be shown to be safe and efficacious, Biofabri, in partnership with IAVI and other collaborators, will ensure that MTBVAC is manufactured and supplied in sufficient quantities globally and is accessible at affordable prices in low- and middle-income countries.<\/p>\n

TB\u00a0<\/strong><\/p>\n

Since the COVID-19 emergency has ended, TB is on track once again to be the deadliest infectious disease in the world. TB killed an estimated\u00a01.3 million people in 2022<\/a>, about 16% of whom were children. Around\u00a010.6 million<\/a>\u00a0people fell ill with TB in 2022, and the disease is one of the 10 leading causes of death worldwide.<\/p>\n

Drug-resistant\/multi-drug resistant TB (DR\/MDR TB) is becoming an increasing threat, with about\u00a0410,000 cases in 2022<\/a>. Treating DR\/MDR TB is lengthy and expensive, often causes debilitating side effects, and is not always successful. A vaccine that prevents TB disease would play an important role in reducing the incidence of DR\/MDR TB, by reducing the transmission of DR\/MDR TB and reducing the use of TB drugs and the emergence of drug-resistant strains.<\/p>\n

MTBVAC<\/strong><\/p>\n

MTBVAC is being developed for two purposes: as a more effective and potentially longer-lasting vaccine than BCG for newborns, and for the prevention of TB disease in adults and adolescents, for whom there is currently no effective vaccine.<\/p>\n

Two Phase II trials have been completed, one\u00a0supported by EDCTP<\/a>\u00a0and sponsored by Biofabri in infants in South Africa, and one\u00a0sponsored by IAVI<\/a>\u00a0and supported by the U.S. National Institutes of Health and the U.S. Department of Defense through its Congressionally Directed Medical Research Program. Results are expected to be published in late 2023.<\/p>\n

Original article: IAVI and Zendal announce funding for efficacy trial of promising TB vaccine candidate in Africa, Zendal (19-12-2023).<\/a><\/h6>\n
\n

For\u00a0BIOGA<\/a>, it is a priority to promote intersectoral collaboration between entities and to power networking activities, both national and international. If you want to know more about us, please click the following\u00a0link<\/a>.<\/strong><\/p>\n