Takeda Pharmaceutical (TYO: 4502) says that data from an 18-month interim analysis of the ongoing Phase II DEN-204 trial of its live, attenuated tetravalent dengue vaccine candidate, TAK-003 (also referred to as TDV), have been published in The Lancet Infectious Diseases. The data showed increased seropositivity rates against dengue virus types 3 and 4 in children who were not previously exposed to infection.
The results of this interim analysis, a pre-planned evaluation of data from an ongoing trial, show that TAK-003 is associated with a reduction in the incidence of dengue in children and adolescents. These data were also presented yesterday at the American Society of Tropical Medicine and Hygiene Annual Meeting, says Takeda, Japan’s largest drugmaker.
“The reduced incidence of dengue in children and adolescents receiving TAK-003 is encouraging, however data from our ongoing Phase III efficacy trial, TIDES, are required to confirm these findings,” Derek Wallace, the lead at Takeda’s dengue program, said in a statement.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze