New TB drugs in the pipeline
Issued by: Simeka TWS Communications
The Global Alliance for TB Drug Development (TB Alliance), a not-for-profit, product development partnership accelerating the discovery and development of new drugs to fight tuberculosis (TB), today announced the advancement of two promising TB treatment candidates into the next phases of research in patients, marking pivotal milestones in the development of faster, simpler regimens.
New York and Cape Town, South Africa, November 8, 2007 –
Moxifloxacin Phase III
A large scale, pivotal Phase III clinical trial in TB patients is beginning with the antibiotic moxifloxacin, already approved for other respiratory indications. The study launching initially at six clinical trial sites in Africa is designed to test whether a four-drug combination regimen including moxifloxacin can reduce treatment time for TB. Earlier studies suggest that combination therapy including moxifloxacin has the potential to shorten the treatment period for drug-susceptible TB from at least six months to four months or less.
PA-824 Phase II
PA-824 is the first novel TB drug candidate developed by a not-for-profit organization to reach clinical trials, and is now in its first test in TB patients in Cape Town. Due to its novel mechanism of action, PA-824 shows promise for treatment of drug-susceptible and drug-resistant TB, and may contribute to treatment shortening when in an effective combination regimen.
Two new promising TB drugs in our portfolio are moving forward in clinical trials, offering patients worldwide the hope of a markedly shorter and better TB treatment, said Dr. Maria C. Freire, CEO and President of the TB Alliance. This is a historic milestone in our accelerated drive to develop new TB drugs that fight the disease in different, faster and better ways to help save millions of lives.
A shorter TB regimen, which may be possible with new drugs such as moxifloxacin and PA-824, should lead to improved patient compliance, helping to maximize cure and limit the emergence of new, resistant strains. Novel compounds like PA-824, which fight TB in different and potentially better ways, are needed to battle the growing threat of drug-resistance.
The development of faster, simpler drug regimens is essential to eliminating the needlessly high burden of TB in Africa and around the world, said Professor Anthony MBewu, President of the South Africa Medical Research Council and a member of the TB Alliance Board of Directors. With the launch of pivotal drug trials in sub-Saharan Africa, where TB takes a particularly devastating toll, the involvement of African researchers and patients is helping pave the way to a revolution in TB treatment.
The moxifloxacin Phase III program, called REMoxTB, is being led by investigators from UCL (University College London) and the British Medical Research Council, and is the pivotal next step in a groundbreaking TB development program between the TB Alliance and Bayer HealthCare AG (Bayer), which developed and markets moxifloxacin globally for other indications. Recruitment for the global REMoxTB program will begin at six sites in Kenya, South Africa, Tanzania and Zambia.
The study will assess whether each of two, four-month regimens substituting moxifloxacin for one of the current standard drugs (ethambutol or isoniazid) is equally effective as the standard six-month therapy in terms of failure and relapse. Phase III studies are needed to build on results of three shorter, smaller Phase II studies, which used similar substitution strategies with moxifloxacin.
In the other key TB Alliance clinical advance, PA-824 is undergoing a Phase IIa Early Bactericidal Activity (EBA) study in TB patients, an evaluation of its short-term potency given as a single drug. Patients enrolled at two sites in Cape Town receive either PA-824 or the standard, four-drug TB treatment for 14 days. If Phase IIa EBA results are positive, the drug will advance to Phase IIb studies in which PA-824 will be given in combination with other current, effective drugs to further test its safety, tolerability and efficacy. Phase I studies of PA-824 in healthy volunteers revealed that the drug is well-tolerated with no dose-limiting adverse events.
Our clinical programme highlights the importance of rigorous standardization in research methods that should serve as a solid foundation for future TB drug development, said Dr. Mel Spigelman, TB Alliance Director of Research and Development. With these clinical advances, and our growing TB drug pipeline, we are confident we will succeed in developing new, novel regimens that are faster-acting, work against drug-resistant disease, and help improve treatment of the growing number of patients co-infected with TB and HIV.
Moxifloxacin is a member of the fluoroquinolone class of antibiotics. It has already been approved for other indications including acute respiratory infections and is the first drug in the TB Alliance portfolio to enter a pivotal registration trial. Moxifloxacin has a different mechanism of action from those of current first-line TB drugs and has demonstrated activity against Mycobacterium tuberculosis (M.tb), the bacillus that causes TB, in both in vitro and in vivo studies. Unlike some existing TB drugs, moxifloxacin does not interact with enzymes that are involved in the body’s handling of antiretroviral therapies used to treat HIV patients.
Moxifloxacin has an excellent safety record, having been used in more than 76 million patients in more than 140 countries. If clinical development is successful, the TB Alliance and Bayer are committed to making moxifloxacin affordable and available for TB patients where it is needed most, especially in developing regions.
PA-824 is a member of the nitroimidazole class. The TB Alliance received worldwide exclusive rights to PA-824 and its analogs for the treatment of TB in a landmark 2002 agreement with Chiron, now part of Novartis, which includes ensuring that the technology will be made available royalty-free in endemic countries. The TB Alliance directs and funds PA-824’s development through a global network of contractors. The US National Institute of Allergy and Infectious Diseases of the National Institutes of Health has provided in-kind support.
The U.S. Food and Drug Administration (FDA) recently approved a request for orphan drug designation for PA-824. The Orphan Drug Act is designed to reduce the costs of developing and registering drugs for some diseases and conditions that are rare in the U.S. The designation confers a number of benefits for the development of PA-824, including a waiver of the nearly $1 million fee usually paid on submission of a New Drug Application. The European Union has just approved similar Orphan Medical Product status for PA-824. The FDA also has granted PA-824 fast-track designation, which is designed to expedite the application and review process for products that have the potential to address a serious or life-threatening condition.
About TB Disease
Tuberculosis (TB) kills someone every 20 seconds more than 1.5 million each year, according to the World Health Organization (WHO).
The WHO estimates about one-third of the world’s population is infected with Mycobacterium tuberculosis (M. tb), the bacillus that causes TB, and the disease is second only to HIV as the leading infectious killer of adults worldwide.
New drugs are critical to ending the needless burden of TB. The current four-drug TB regimen, a product of the best scientific advances of the 1960s, works for drug-susceptible TB as long as patients complete at least six months of treatment. The problem is, many do not or cannot. As patients start to feel better within a few weeks, many find it difficult to complete the cumbersome treatment or maintain access to the drugs. This can lead to the emergence of TB strains that are resistant to first-line and even second-line drugs.
Reducing the time it takes for patients to finish the full course of drugs needed for a cure would make treatment much easier for patients and healthcare workers, saving lives and money, and curbing the threat of deadly drug-resistance.
About The Global Alliance for TB Drug Development
The Global Alliance for TB Drug Development (TB Alliance) is a not-for-profit, product development partnership accelerating the discovery and development of new TB drugs that will shorten treatment, be effective against susceptible and resistant strains, be compatible with antiretroviral therapies for those HIV-TB patients currently on such therapies, and improve treatment of latent infection.
Working with public and private partners worldwide, the TB Alliance is leading the development of the most comprehensive portfolio of TB drug candidates in history, and is committed to ensuring that approved new regimens are affordable, adopted and available to those who need them.
The TB Alliance operates with funding from the Bill & Melinda Gates Foundation, the Rockefeller Foundation, Irish Aid, the Netherlands Ministry of Foreign Affairs (DGIS), the United Kingdom Department for International Development (DFID), and the United States Agency for International Development (USAID). For more information on TB drug development and the TB Alliance, please visit www.tballiance.org.
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