} Faster review for new respiratory issue therapy? - Strand
  • Home
  • Insights
  • Faster review for new respiratory issue therapy?

2/7/2019 - Posted in  Pharmaceutical Affairs

Faster review for new respiratory issue therapy?

Our expert's opinion

"Gene Therapy is a technique that modifies a person’s gene to treat or cure a disease.

It replaces or inactivates a disease-causing gene or it introduces a new or modified gene into the body, a technique that could be used to treat cancer and genetic and infectious diseases.

Nevertheless, this raises an inevitable question: could this cause any undesirable and unpredictable outcomes?

The first gene therapy trial was run more than 30 years ago, and the earliest studies showed that gene therapy could have various health risks such as toxicity, inflammation, and cancer.

Since then, researchers have been working to ensure that gene therapy treatments are as safe as possible. However, it also raises ethical concerns: who decides what is considered a disorder?

For now, the US Food and Drug Administration has approved only a few gene therapy products.

This progress shows how far researchers go to improve people’s lives and although it demonstrates a promising future, we are still learning a lot about it."

-  Marie Copée, Consultant

What is Gene Therapy?

Gene therapy is a medical approach that treats or prevents disease by correcting the underlying genetic problem. Gene therapy techniques allow doctors to treat a disorder by altering a person’s genetic makeup instead of using drugs or surgery.

The earliest method of gene therapy, often called gene transfer or gene addition, was developed to:

Introduce a new gene into cells to help fight a disease.
Introduce a non-faulty copy of a gene to stand in for the altered copy causing disease.
Later studies led to advances in gene therapy techniques. A newer technique, called genome editing (an example of which is CRISPR-Cas9), uses a different approach to correct genetic differences. Instead of introducing new genetic material into cells, genome editing introduces molecular tools to change the existing DNA in the cell. Genome editing is being studied to:

Fix a genetic alteration underlying a disorder, so the gene can function properly.
Turn on a gene to help fight a disease.
Turn off a gene that is functioning improperly.
Remove a piece of DNA that is impairing gene function and causing disease.
Gene therapies are being used to treat a small number of diseases, including an eye disorder called Leber congenital amaurosis and a muscle disorder called spinal muscular atrophy. Many more gene therapies are undergoing research to make sure that they will be safe and effective. Genome editing is a promising technique also under study that doctors hope to use soon to treat disorders in people.

Source: Medline Plus

Other insights in Pharmaceutical Affairs