$3.5 million is the price for the world's most expensive drug
Australian pharmaceutical company CSL on November 23 set the list price of its drug to treat hereditary hemophilia B at $3.5 million per dose, Reuters reported.
Browse ScienceInfo articles and explainers related to Gene Therapy.
40 published items.
Australian pharmaceutical company CSL on November 23 set the list price of its drug to treat hereditary hemophilia B at $3.5 million per dose, Reuters reported.
The US FDA has approved the world's most expensive drug at a price of 4.25 million USD per dose to treat rare diseases in children.
The new gene therapy will have to go through many more stages before it is officially tested in humans.
Genetic therapy for Novartis spinal muscular atrophy costs more than $ 2 million a course.
When the cell matures, many of its genes will become permanently inactive. Errors in the process of 1 gene can cause disease.
Along with the advancement of medicine and the desire to conquer the disease of the century, 2011 marked many breakthroughs in HIV treatment.
For the first time, scientists created monkeys from cells of many separate embryos. But the monkey was born after researchers combined many cells of different embryos an…
5 scientists were voted as the outstanding faces of 2015 by great achievements in the fields of science in the hope of improving human life better.
This is the first time that successful researchers have replaced damaged retinal cells, giving hope that someday in the near future can be applied to humans.
Researchers at the University of California (UCLA) in the US have published a study that said a gene therapy using stem cells of hematopoietic patients could extend prot…
Blindness can be cured by using gene therapy to reprogram cells in the retina to make these cells possible.
In a recent study, scientists at Oregon State University (OSU) studied proteins called otoferlin located in the inner ear cochlea.
Scientists at Methodist Reseach Research Institute in Houston (USA) claim to have reversed many signs of aging in cells from children with premature aging (progeria).
This research helps open up the hope of treating this autoimmune disease, which affects millions of children and young people around the world.