CRISPR Will Allow to Cure Genetic Diseases That Were Previously Incurable
The MHRA has approved Casgevy to treat sickle cell disease (SCD) and transfusion-dependent beta thalassaemia. These are lifelong genetic disorders caused by mutations in the genes that code for haemoglobin, the protein red blood cells need to transport oxygen around the body. CRISPR could treat a common form of inherited blindness. The 2020 Nobel Prize in Chemistry has gone to two women who developed a gene-editing tool called CRISPR-Cas9, which cuts DNA like molecular scissors.
The drug “Lenacapavir” provides long-term protection and guarantees 100% protection against HIV infection
The American company Gilead Sciences, Inc. has conducted the first clinical trials of the last, third phase of its new drug for the human immunodeficiency virus (HIV) lenacapavir. And the medicine has shown absolute effectiveness: according to the manufacturer, this is the first medication in history that protects against HIV by 100%.