Exciting news from the Biden-Harris Administration as they prioritize sickle cell disease for groundbreaking gene therapies! Find out more here.
In a groundbreaking move, the Biden-Harris Administration has announced the prioritization of sickle cell disease for Cell and Gene Therapy (CGT) Access Model. This decision marks a significant step towards revolutionizing the treatment landscape for individuals with sickle cell anemia. The innovative approach is aimed at enhancing access to cutting-edge gene therapies, addressing the challenges faced by those with sickle cell disease.
Furthermore, the Centers for Medicare and Medicaid Services (CMS) are set to negotiate outcomes-based agreements to facilitate Medicaid coverage of these life-changing treatments. By focusing on outcomes and costs, CMS aims to ensure that individuals with sickle cell disease can benefit from transformative therapies without financial constraints.
Adding to the excitement, Comer Children's Hospital in Chicago will be among the pioneering centers offering newly approved gene therapies for sickle cell disease. This development brings hope to many patients and underscores the growing importance of tailored treatments for genetic disorders like sickle cell anemia.
Amidst these advancements, concerns loom over the affordability of these innovative therapies. With significant price tags, the accessibility of gene editing treatments for sickle cell disease remains a pressing issue. Stakeholders continue to navigate the delicate balance between providing state-of-the-art care and managing the financial implications, striving for a healthcare system that prioritizes both quality and equity.
Did you know that the Food and Drug Administration recently approved breakthrough gene editing therapies for sickle cell disease? These treatments offer promising solutions for individuals facing the challenges of this inherited blood cell disorder. Additionally, the focus on outcomes-based agreements in Medicaid coverage highlights the evolving landscape of healthcare pricing and reimbursement, aiming to make revolutionary treatments more accessible to those in need.
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The Biden-Harris Administration announced today that sickle cell disease (SCD) will be the first focus of the Cell and Gene Therapy (CGT) Access Model, ...
The โaccess modelโ is designed to blunt the cost that state Medicaid programs would pay for these curative treatments.
The Biden-Harris Administration announced today that sickle cell disease (SCD) will be the first focus of the Cell and Gene Therapy (CGT) Access Model.
This is an inherited blood cell disorder, and it can cause debilitating pain, even strokes. The Food and Drug Administration approved breakthrough gene editing ...
Comer Children's Hospital will be one of the first centers in the U.S. to offer two recently approved gene therapies for sickle cell disease.
People with sickle cell disease are thrilled there are now approved gene therapies for the inherited blood disorder, but the cost has them wondering if ...
โMany of the more than 100,000 Americans with sickle cell disease face difficulty accessing effective health care and groundbreaking treatments," said ...
This is an inherited blood cell disorder, and it can cause debilitating pain, even strokes. The Food and Drug Administration approved breakthrough gene editing ...
The Centers for Medicare and Medicaid Services will enter talks with manufacturers to come up with a pricing and rebate scheme that will tie the gene ...
The Centers for Medicare and Medicaid Services will pursue so-called outcomes-based agreements that would put discounts or rebates in place on two new ...
The FDA in December also approved Vertex Pharmaceuticals' $2.2 million Casgevy sickle cell disease treatment. The treatments are intended as cures for the more ...
Sickle cell disease (SCD) will be the first focus of the Cell and Gene Therapy (CGT) Access Model; the FTC has challenged the validity of over 100 drug ...