Sanofi to comply with Philippines FDA post Dengvaxia clearance delay
Date: 2018-01-05   Author: Saif Ali Bepari  Category: #news

Sanofi to comply with Philippines FDA post Dengvaxia clearance delay

In what may be regarded as a severe blow to the French pharmaceutical giant Sanofi’s expansion plans in South East Asia, the Food and Drug Administration of Philippines has reportedly suspended clearance for the firm’s dengue vaccine Dengvaxia. The regulator has further levied a symbolic fine of USD 2,000 on the drug maker citing infringements on product registration and marketing practices.

Sanofi had released an advisory last year which reportedly noted that as per its re-evaluation of clinal trials, Dengvaxia is effective in preventing reoccurrence of dengue infections, however administering the vaccine to those with no prior infections could expose them to risk of a fatal strain of the disease. Apparently, the revelation led to widespread concerns across Philippines which, as per reliable sources, spent around USD 70 million on a public immunization programme in 2016 to lower the rising number of dengue cases across the nation.

The concerns compelled the government to institute two congressional inquiries and a criminal investigation in which several pharma experts expressed their reservations pertaining to Sanofi’s dengue vaccine. The Government of Philippines has also ordered the pharma giant to halt its sale, marketing, and distribution of its vaccine. As per official data, Philippines has been adversely affected by the disease with a massive 200,000 dengue cases being reported each year. For the record, the World Health Organization recommends the introduction of Dengvaxia only in the nations where epidemiological data indicates a high burden of disease.

Meanwhile, Sanofi released a statement confirming that it has received a notice from the FDA which mentions a total of a one-year suspension for its marketing authorization of Dengvaxia. The statement further states that the suspension is linked to the firm’s non-compliance with post-marketing regulations and is not associated with the vaccine’s portfolio. However, it has been reported that post the clearance delay, Sanofi has promised 100% cooperation with the FDA’s regulations regarding the drug.



About Author


Saif Ali Bepari

Saif Ali Bepari

Saif currently works as a content writer at Algosonline. A Computer Science graduate who has a zest for writing over coding, commenced his journey in the writing industry as a freelancer. Having had a prior freelance experience, he has tinkered with creative writing, ...

Read More

More from Saif


Post Recommendents

Nomura Holdings to acquire U.S. M&A firm Greentech in US$92m deal
Author: Pankaj Singh

Nomura Holdings, a financial holding company in Japan, has recently announced that it will buy Greentech Capital Advisors, a mergers and acquisitions advisory company from the U.S. that specializes in renewable energy. This will be the company&rsq...


Perfect Day raises $140 Mn in a Series C funding round led by Temasek
Author: Saipriya Iyer

Perfect Day, a US-based food technology startup that has innovated new processes of creating dairy products by using casein, reportedly announced that it raised $140 million in a Series C funding round. This investment...


Current Health raises $11.5 million in Series A funding round
Author: Pankaj Singh

Current Health, a renowned New York based universal patient management platform, reportedly announced that it has closed a $11.5 million Series A funding round which was co-led by UK based MMC Ventures.