Winter 2017 - Integrated Care

FDA Approves First Human Trial of a Zika Vaccine

The U.S. Food and Drug Administration has approved the first human trial of an experimental Zika virus vaccine. Developed by Inovio Pharmaceuticals and GeneOne Life Science, the DNA-based vaccine known as GLS-5700 will be given to 40 people in a Phase I trial that began in July. Preclinical data from animal studies suggested that the vaccine could include a strong immune response that might protect against mosquito-transmitted Zika. The human study, however, will not test how effective the vaccine is at fighting the Zika virus. Instead, the trial will test the vaccine’s safety and appropriate dosage levels. If found to be safe, larger trials of the vaccine will test its efficacy, and those will take years to complete.

References

  1. Mole B. First Experimental Zika Vaccine Gets Nod from FDA, Moves to Human Trials. Ars Technica, June 20, 2016. Accessed at arstechnica.com/science/2016/06/first-experimental-zika-vaccine-gets-nod-from-fdamoves-to-human-trials.
BSTQ Staff
BioSupply Trends Quarterly [BSTQ] is the definitive source for industry trends, news and information for the biopharmaceuticals marketplace. With timely and critical information, each themed issue covers topics ranging from product breakthroughs, industry insights and innovations, up-to-the-minute news on the latest clinical trials, accessibility, and service and safety concerns.