Sunday, February 13, 2011 11:21:08 AM
Times Of India Examines Dengue Vaccine Trials
Thursday, February 10, 2011
India could soon become a site for clinical trials to evaluate the effectiveness of a dengue vaccine, the Times of India reports. According to the drug controller general of India (DCGI), vaccine maker Sanofi Pasteur recently submitted a proposal to test the vaccine to the country. If approved, India would be the latest country to join in studies of the vaccine's effectiveness in adults and children, which are already taking place in Australia, Colombia, Honduras, Mexico, Peru, Philippines, Puerto Rico, Singapore, Thailand and Vietnam, according to the newspaper.
"There is no vaccine available for dengue fever that is a threat to around three billion people, mostly in Latin America and Asia," the Times of India writes, adding, Sanofi's vaccine "targets all four virus serotypes circulating in the U.S., Asia and Latin America."
"In India, the two-year trial will involve 1,000 people," explained Jean Lang of Sanofi's vaccine program. "We will first try the three-shot vaccine on the 2-45 age group. After reviewing that result, we will use it on those between 9 months and 65 years. We want to see the immunogenicity response in Indians," he added.
According to Lang, the company hopes to "have a viable, effective and safe dengue vaccine by 2015," but will be watching closely as the results of an ongoing efficacy trial involving 4,000 children in Thailand wrap up. Lang said the data from that trial are expected to be available by the end of 2012. "Of the estimated 220 million people infected annually, two million – mostly children – develop dengue hemorrhagic fever (DHF). Globally, the projected number of annual dengue infections is estimated between 50-100 million, with 24,000 deaths, who are mainly children," according to the Times of India (Sinha, 2/10).
The Kaiser Daily Global Health Policy Report is published by the Kaiser Family Foundation. © 2011 Henry J. Kaiser Family Foundation. All rights reserved.
Thursday, February 10, 2011
India could soon become a site for clinical trials to evaluate the effectiveness of a dengue vaccine, the Times of India reports. According to the drug controller general of India (DCGI), vaccine maker Sanofi Pasteur recently submitted a proposal to test the vaccine to the country. If approved, India would be the latest country to join in studies of the vaccine's effectiveness in adults and children, which are already taking place in Australia, Colombia, Honduras, Mexico, Peru, Philippines, Puerto Rico, Singapore, Thailand and Vietnam, according to the newspaper.
"There is no vaccine available for dengue fever that is a threat to around three billion people, mostly in Latin America and Asia," the Times of India writes, adding, Sanofi's vaccine "targets all four virus serotypes circulating in the U.S., Asia and Latin America."
"In India, the two-year trial will involve 1,000 people," explained Jean Lang of Sanofi's vaccine program. "We will first try the three-shot vaccine on the 2-45 age group. After reviewing that result, we will use it on those between 9 months and 65 years. We want to see the immunogenicity response in Indians," he added.
According to Lang, the company hopes to "have a viable, effective and safe dengue vaccine by 2015," but will be watching closely as the results of an ongoing efficacy trial involving 4,000 children in Thailand wrap up. Lang said the data from that trial are expected to be available by the end of 2012. "Of the estimated 220 million people infected annually, two million – mostly children – develop dengue hemorrhagic fever (DHF). Globally, the projected number of annual dengue infections is estimated between 50-100 million, with 24,000 deaths, who are mainly children," according to the Times of India (Sinha, 2/10).
The Kaiser Daily Global Health Policy Report is published by the Kaiser Family Foundation. © 2011 Henry J. Kaiser Family Foundation. All rights reserved.
Recent NNVC News
- Phase II Clinical Trial of Monkeypox Treatment by NV-387 to Commence Soon, Announces NanoViricides • ACCESS Newswire • 04/01/2026 12:30:00 PM
- NanoViricides Presenting at NIBA's 152nd Investment Conference in Fort Lauderdale, FL March 12, 2026 - Announces Manufacture of Phase II Clinical Product NV-387 Oral Gummies is Complete • ACCESS Newswire • 03/11/2026 12:30:00 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/17/2026 09:30:47 PM
- MPox Orphan Drug Designation Application Filed for NV-387, Declares NanoViricides • ACCESS Newswire • 02/12/2026 01:30:00 PM
- Measles Orphan Drug Designation Application Filed for NV-387, Declares NanoViricides • ACCESS Newswire • 02/10/2026 01:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 12/30/2025 09:30:18 PM
- Form DEL AM - Delaying amendment • Edgar (US Regulatory) • 12/16/2025 09:30:05 PM
- Form S-3 - Registration statement under Securities Act of 1933 • Edgar (US Regulatory) • 12/15/2025 09:26:07 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/26/2025 09:30:33 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/14/2025 09:32:10 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/12/2025 07:54:28 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/12/2025 04:29:54 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/01/2025 09:07:54 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 09/29/2025 08:33:17 PM
