A sponge-like implant in mice helped guide a treatment that slowed or stopped a degenerative condition similar to multiple sclerosis in humans. It also gave researchers a look at how primary ...
The Medical University of South Carolina is expanding its access to state-supported Sickle Cell programs for “warriors,” or ...
An SCD patient in Bahrain received the gene-editing therapy Casgevy, marking the first time the treatment has been given outside the U.S.
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The high cost of sickle cell gene therapies is pushing private insurers and Medicaid programs to develop new payment models.
A team of Bahraini specialists has successfully treated a patient with sickle cell disease using the revolutionary CRISPR gene-editing technology, making Bahrain the first country outside the United ...
Researchers developed a new gene-editing strategy that dramatically boosts the effectiveness of gene therapies in the liver, a breakthrough that could lead to new treatments for about 700 genetic ...
This achievement follows Bahrain’s landmark decision on 2 December 2023 to become the second country globally and the first ...
Bone marrow transplantation is a costly procedure. Depending on the type of transplant the rate may vary from ₹7 lakh to ₹50 ...
Researchers at the New York Blood Center have made a breakthrough in understanding the body’s autoimmune response to sickle ...
Research and Development (R&D) Expenses: R&D expenses were $82.8 million for the fourth quarter of 2024, compared to $77.5 million for the fourth quarter of 2023, and $301.3 million for the full year ...
No doubt 2025 will usher in many more advances in CRISPR therapies, thanks to the FDA’s new Platform Technology Designation ...
New York–based hematologist-oncologist and clinical researcher works to lower the barriers to enrolling in clinical trials.
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