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Read of the following leaflet and mark the letter A, B, C or D on your answer sheet to indicate the option that best fits each of the number...

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Read of the following leaflet and mark the letter A, B, C or D on your answer sheet to indicate the option that best fits each of the numbered blanks from 7 to 12.

CASGEVY—A NEW HOPE FOR SICKLE CELL DISEASE

Revolutionary Gene-Editing Therapy Now Available on the NHS

Great news for patients with severe sickle cell disease!

        On 31 January 2025, NICE approved Casgevy (exagamglogene autotemcel), a (7)_________ treatment for eligible NHS patients aged 12 and over.

        How Does It Work?

        This innovative treatment uses CRISPR gene-editing technology to transform your own stem cells. (8)_________ process involves collecting your cells, editing them in a laboratory, and infusing them back into your body. (9)_________ the cells are your own, there is absolutely no risk of rejection by your immune system.

        Who Is Eligible?

        Casgevy is suitable for patients who need a stem-cell transplant but cannot find a matched (10)_________. Many current treatments only control symptoms and often cause (11)_________ side effects for patients.

        Why This Matters

        For thousands of SCD patients, this therapy could be the light at the end (12)_________ the tunnel after years of suffering. SCD disproportionately affects people from African, Caribbean, Middle Eastern, and South Asian backgrounds—making this approval a significant step toward reducing health inequalities.

        Take Action Today

Contact your GP or specialist to discuss whether Casgevy is right for you.

        Learn more: www.nhs.uk/casgevy-information

        Find your nearest treatment centre: www.nhs.uk/scd-centres

This therapy is offered via a managed access scheme. Eligibility criteria apply.

Together, we can fight sickle cell disease!

https://www.nice.org.uk/z

Question 7:A. gene therapy groundbreaking                         B. groundbreaking gene therapy

C. groundbreaking therapy gene                         D. therapy groundbreaking gene 

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