Matching articles for "Jakafi"
Axatilimab (Niktimvo) for Chronic Graft-Versus-Host Disease (online only)
The Medical Letter on Drugs and Therapeutics • November 11, 2024; (Issue 1715)
Axatilimab-csfr (Niktimvo – Incyte), a colony
stimulating factor-1 receptor-blocking antibody, has
been approved by the FDA for intravenous treatment
of chronic graft-versus-host disease (cGVHD)...
Axatilimab-csfr (Niktimvo – Incyte), a colony
stimulating factor-1 receptor-blocking antibody, has
been approved by the FDA for intravenous treatment
of chronic graft-versus-host disease (cGVHD) after
failure of at least 2 lines of systemic therapy in patients
weighing ≥40 kg. Corticosteroids are generally the
first-line treatment for cGVHD. The oral kinase
inhibitors ibrutinib (Imbruvica), ruxolitinib (Jakafi),
and belumosudil (Rezurock) are also approved for
treatment of cGVHD. Extracorporeal photopheresis
has been used off-label.
Ritlecitinib (Litfulo) for Severe Alopecia Areata
The Medical Letter on Drugs and Therapeutics • November 27, 2023; (Issue 1690)
The FDA has approved ritlecitinib (Litfulo – Pfizer), an
oral JAK and TEC kinase family inhibitor, for treatment
of severe alopecia areata in patients ≥12 years old.
Ritlecitinib is the second oral drug...
The FDA has approved ritlecitinib (Litfulo – Pfizer), an
oral JAK and TEC kinase family inhibitor, for treatment
of severe alopecia areata in patients ≥12 years old.
Ritlecitinib is the second oral drug to be approved
in the US for treatment of severe alopecia areata;
baricitinib (Olumiant), a JAK inhibitor, is approved
only for use in adults.
Baricitinib (Olumiant) for Severe Alopecia Areata
The Medical Letter on Drugs and Therapeutics • September 5, 2022; (Issue 1658)
The oral Janus kinase (JAK) inhibitor baricitinib
(Olumiant – Lilly), which was previously approved by
the FDA for treatment of moderately to severely active
rheumatoid arthritis and treatment of COVID-19...
The oral Janus kinase (JAK) inhibitor baricitinib
(Olumiant – Lilly), which was previously approved by
the FDA for treatment of moderately to severely active
rheumatoid arthritis and treatment of COVID-19 in
certain hospitalized adults, has now been approved
for treatment of severe alopecia areata in adults.
Baricitinib is the first systemic treatment to be
approved in the US for this indication.
Ruxolitinib (Opzelura) for Atopic Dermatitis
The Medical Letter on Drugs and Therapeutics • January 24, 2022; (Issue 1642)
The FDA has approved a 1.5% topical cream
formulation of the Janus kinase (JAK) inhibitor
ruxolitinib (Opzelura – Incyte) for short-term, non-continuous
chronic treatment of mild to moderate
atopic...
The FDA has approved a 1.5% topical cream
formulation of the Janus kinase (JAK) inhibitor
ruxolitinib (Opzelura – Incyte) for short-term, non-continuous
chronic treatment of mild to moderate
atopic dermatitis (AD) in non-immunocompromised
patients ≥12 years old whose disease has not been
adequately controlled with other topical prescription
drugs. Ruxolitinib is the first JAK inhibitor to be
approved for topical use and the first to be approved
in the US for treatment of AD. An oral formulation
of ruxolitinib (Jakafi) is approved for treatment of
myelofibrosis, polycythemia vera, and graft-versus-host
disease.
Table: Treatments Considered for COVID-19 (Archived) (online only)
The Medical Letter on Drugs and Therapeutics • April 6, 2020; (Issue 1595)
...
View the Table: Treatments Considered for COVID-19
Ruxolitinib (Jakafi) for Myelofibrosis
The Medical Letter on Drugs and Therapeutics • April 2, 2012; (Issue 1387)
The FDA has approved ruxolitinib (Jakafi – Incyte), a
janus-associated kinase (JAK) inhibitor, for treatment
of myelofibrosis. Jakafi is the first JAK inhibitor to be
approved for any indication and the...
The FDA has approved ruxolitinib (Jakafi – Incyte), a
janus-associated kinase (JAK) inhibitor, for treatment
of myelofibrosis. Jakafi is the first JAK inhibitor to be
approved for any indication and the only drug
approved for treatment of myelofibrosis.