Articles by Sabrina Ahle
New legislation would set time limits around FDA accelerated approvals.
The designation was granted to ex vivo investigational T-cell receptor therapy NTLA-5001.
The FDA has accepted the sNDA for ivosidenib tablets as a proposed treatment for previously untreated IDH1-mutated AML.
The FDA has published draft recommendations for potential manufacturers of gene therapy products.
Mocravimod is a sphingosine 1 phosphate receptor modulator.
Researchers shared additional data on the immune response of patients with chronic myeloid leukemia to COVID-19 infection and ...
At least one-quarter of patients experienced arterial occlusive events (AOE), but rates varied depending on the approach.
Researchers surveyed the reasons for low recruitment and early closure of the UK National Cancer Research Institute’s ...
The FDA has granted accelerated approval to pacritinib for the treatment of adult patients with intermediate or high-risk.
Many side effects of the COVID-19 pandemic have disproportionately impacted older Americans.
According to a recent HHS report, the percentage of uninsured Black Americans has decreased since the ACA became law in 2010.
Oxford Biodynamics has announced the US launch of the clinical blood test.
Cilta-cel has been approved by the FDA for the treatment of patients with relapsed or refractory multiple myeloma who have ...
The EU proposed the first international regulation for artificial intelligence.
Researchers examined survival rates by age in patients with Hodgkin lymphoma receiving response-adapted therapy on ...
In patients with high-risk essential thrombocythemia and polycythemia vera, both hydroxyurea and pegylated interferon-α.
A recent study of brexu-cel supports its use for the treatment of MCL.
Post-transplant response-adapted consolidation therapy with Dara-KRd using MRD led to high rates of MRD negativity in ...
After failing to complete the requisite confirmatory trials following accelerated approval, Gilead has announced it will ...
Allogene Therapeutics has been cleared by the U.S. Food and Drug Administration (FDA) to resume trials of its allogeneic ...
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