(Reuters) – Takeda Pharmaceutical’s experimental dengue vaccine has produced promising long-term results in clinical tests, boosting the Japanese company’s global hopes for a product that will take on Sanofi’s Dengvaxia.
Japan’s top drugmaker has become more international under its French CEO Christophe Weber, who took over in 2015. Its vaccine to prevent the mosquito-borne fever is a chance to make a significant impact on a global neglected tropical disease.
Sanofi’s Dengvaxia is the first-ever approved vaccine for dengue, but it is not perfect and did not protect equally against the four different types of the virus in clinical tests.
The latest 18-month data published in the journal Lancet Infectious Diseases showed Takeda’s vaccine TAK-003 produced sustained antibody responses against all four virus strains, regardless of previous dengue exposure and dosing schedule.
Symptomatic dengue was recorded in 21, or 1.3 percent, of 1,596 Asian and Latin America children and adolescents vaccinated with TAK-003 compared with nine, or 4.5 percent, of 198 placebo recipients.
In April this year, Takeda completed enrolment for a final-stage Phase III trial – the largest clinical study in the company’s history – that will test the experimental vaccine on 20,100 subjects in eight countries in Latin America and Asia where dengue is endemic.
Results from the Phase III trial are expected in 2018.
Although dengue is not as serious as malaria, it is spreading rapidly in many parts of the world. The virus kills about 20,000 people a year and infects hundreds of millions.
Sanofi initially had high hopes for its dengue vaccine, touting it as a potential $1-billion-a-year-plus product, but initial sales last year were only 55 million euros ($64 million) and industry analysts have been dialing back expectations.
Current consensus analyst forecasts point to annual sales of around 360 million euros for Dengvaxia by 2022, Thomson Reuters data shows.
Reporting by Ben Hirschler; Editing by Hugh Lawson