Report ID: SQMIG35A2273
Report ID:
SQMIG35A2273 |
Region:
Global |
Published Date: March, 2024
Pages:
219
|
Tables:
63 |
Figures:
75
In January 2024, the Competition and Markets Authority (CMA) started an investigation into Vifor Pharma (Vifor), a worldwide pharmaceutical company, regarding its alleged anti-competitive behavior in the provision of intravenous (IV) iron deficiency treatments for patients under the National Health Service (NHS) in the UK.
In September 2023, Akebia Therapeutics®, Inc. declared that Australia's Therapeutic Goods Administration (TGA) has approved Vafseo® (vadadustat), an oral hypoxia-inducible factor prolyl hydroxylase inhibitor. This approval is for anemia treatment related to chronic kidney disease (CKD) in adults undergoing chronic maintenance dialysis.
In June 2023, Daiichi Sankyo, Inc. and American Regent, Inc., a Daiichi Sankyo Group company, reported that the U.S. The Food and Drug Administration (FDA) approved INJECTAFER (ferric carboxymaltose injection) for treating iron deficiency in adult patients with heart failure categorized as New York Heart Association class II/III to enhance exercise capacity.
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Report ID: SQMIG35A2273