UK authorizes gene therapy for blood disorders in world first
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[November 16, 2023]
LONDON (Reuters) - Britain has authorized a gene therapy that
aims to cure sickle-cell disease and another type of inherited blood
disorder for patients aged 12 and over, the country's medical regulator
said on Thursday, becoming the first in the world to do so.
Casgevy is the first medicine to be licensed that uses the gene-editing
tool CRISPR, which won its inventors the Nobel Prize in 2020, Britain's
Medicines and Healthcare products Regulatory Agency (MHRA) said.
Sickle cell disease and β-thalassemia are genetic conditions caused by
errors in the genes for haemoglobin, which is used by red blood cells to
carry oxygen around the body.
"Both sickle cell disease and β-thalassemia are painful, life-long
conditions that in some cases can be fatal," MHRA Interim Director
Julian Beach said in the statement.
In clinical trials Casgevy has been found to restore healthy haemoglobin
production in the majority of participants with sickle-cell disease and
transfusion-dependent β -thalassaemia, relieving the symptoms of
disease, Beach added.
The MHRA said no significant safety concerns were identified during the
trials, adding that it was closely monitoring the safety of the
medicine.
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A sign hangs in front of the world headquarters of Vertex
Pharmaceuticals in Boston, Massachusetts, U.S., October 23, 2019.
REUTERS/Brian Snyder
The medicine is administered by
taking stem cells out of a patient’s bone marrow and editing a gene
in the cells in a laboratory, with the modified cells then infused
back into the patient after conditioning treatment to prepare the
bone marrow.
U.S.-based companies Vertex Pharmaceuticals and CRISPR Therapeutics
welcomed the approval in a separate statement.
"I hope this represents the first of many applications of this Nobel
Prize winning technology to benefit eligible patients with serious
diseases," said CRISPR CEO Samarth Kulkarni said.
(Reporting by Muvija M; editing by Sarah Young)
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