• Hausa Edition
  • Podcast
  • Conferences
  • LeVogue Magazine
  • Business News
  • Print Advert Rates
  • Online Advert Rates
  • Contact Us
Tuesday, September 8, 2026
Leadership Newspapers
No Result
View All Result
  • Home
  • News
  • Politics
  • Business
  • Sport
    • Football
  • Health
  • Entertainment
  • Education
  • Opinion
    • Editorial
    • Columns
  • Others
    • LeVogue Magazine
    • Conferences
    • National Economy
  • Contact Us
Hausa Edition
  • Home
  • News
  • Politics
  • Business
  • Sport
    • Football
  • Health
  • Entertainment
  • Education
  • Opinion
    • Editorial
    • Columns
  • Others
    • LeVogue Magazine
    • Conferences
    • National Economy
  • Contact Us
No Result
View All Result
Leadership Newspapers
No Result
View All Result

US Agency Approves Cure For Sickle Cell Disease

Pamela Ephraim by Pamela Ephraim
3 years ago
in Health
images 13 1 jpeg
Share on WhatsAppShare on FacebookShare on XTelegram

The United States Food and Drug Administration (FDA) has approved a treatment for sickle cell disease.

The therapy, called Casgevy, from Vertex Pharmaceuticals and CRISPR Therapeutics, is the first medicine to be approved in the United States that uses the gene-editing tool CRISPR, which won its inventors the Nobel Prize in Chemistry in 2020.

The approval marks the first of two potential breakthroughs for the inherited blood disorder.

The FDA on Friday also approved a second treatment for sickle cell disease, called Lyfgenia, a gene therapy from drugmaker Bluebird Bio. Both treatments work by genetically modifying a patient’s own stem cells.

Until now, the only known cure for sickle cell disease was a bone marrow transplant from a donor, which carries the risk of rejection by the immune system, in addition to the difficult process of finding a matching donor.

RELATED NEWS

How I Transformed NAFDAC From ‘Good-For-Nothing’ Agency — DG

World Bank Invests N1.5bn To Fight Malaria In Ondo

Sokoto Govt Urged To Sustain Primary Healthcare Reforms

Casgevy, which was approved for people ages 12 and older, removes the need for a donor. Using CRISPR, it edits the DNA found in a patient’s stem cells to remove the gene that causes the disease.

According to NBC News, the new therapy costs $2.2 million per patient.

We’ve got the edge. Get real-time reports, breaking scoops, and exclusive angles delivered straight to your phone. Don’t settle for stale news. Join LEADERSHIP NEWS on WhatsApp for 24/7 updates →

Join Our WhatsApp Channel


Pamela Ephraim

Pamela Ephraim

OTHER NEWS UPDATES

How I Transformed NAFDAC From ‘Good-For-Nothing’ Agency — DG
Health

How I Transformed NAFDAC From ‘Good-For-Nothing’ Agency — DG

5 hours ago
World Bank Invests N1.5bn To Fight Malaria In Ondo
Health

World Bank Invests N1.5bn To Fight Malaria In Ondo

1 day ago
Governor Aliyu Unveils N526bn 2025 Budget
Health

Sokoto Govt Urged To Sustain Primary Healthcare Reforms

2 days ago
Next Post
Akwaba: Yemi Alade Relishes Contribution To 2024 AFCON Official Theme Song

Akwaba: Yemi Alade Relishes Contribution To 2024 AFCON Official Theme Song

Advertisement

LATEST UPDATE

‎Baby Factory: I Sold My Newborn Twins For N300,000, Stole 19 Children — Suspect

2 hours ago

Nigerian Scientist Wins $100,000 NLNG Prize for AI-powered MRI Tech

3 hours ago

Kwara Gov, Speaker Condole With Leadership Correspondent Olesin Over Mother’s Death

3 hours ago

Food Security: Adamu Empowers Farmers, Assures Of Mechanised Farming

4 hours ago

Kaduna Govt Harps On Synergy Between Boards And Management

4 hours ago
Load More
Advertisement
Facebook Twitter Instagram Youtube Whatsapp

© 2026 LEADERSHIP Media Group - All Rights Reserved | Hausa | Online Casino.

No Result
View All Result
  • Home
  • News
  • Politics
  • Business
  • Sport
    • Football
  • Health
  • Entertainment
  • Education
  • Opinion
    • Editorial
    • Columns
  • Others
    • LeVogue Magazine
    • Conferences
    • National Economy
  • Contact Us

© 2026 LEADERSHIP Media Group - All Rights Reserved | Hausa | Online Casino.