Search Results for "tocilizumab"
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Searched for tocilizumab. Results 21 to 24 of 24 total matches.
See also: Actemra
Tofacitinib (Xeljanz) for Rheumatoid Arthritis
The Medical Letter on Drugs and Therapeutics • Jan 07, 2013 (Issue 1407)
IV twice, 2 weeks apart6 2599.447
Tocilizumab – Actemra (Genentech) 80, 200, 400 mg single-use vials ...
The FDA has approved tofacitinib (toe” fa sye’ ti nib;
Xeljanz – Pfizer), an oral Janus kinase (JAK) inhibitor, for
treatment of adults with moderately to severely active
rheumatoid arthritis (RA) who have had an inadequate
response to or are intolerant of methotrexate. Ruxolitinib
(Jakafi) is the only other JAK inhibitor available in the
US; it is FDA-approved for treatment of myelofibrosis.
Tisagenlecleucel (Kymriah) for ALL
The Medical Letter on Drugs and Therapeutics • Oct 23, 2017 (Issue 1532)
inhibitor tocilizumab (Actemra), with or without other
anti-inflammatory agents.5 No CRS-related deaths ...
The FDA has approved tisagenlecleucel (Kymriah —
Novartis), an individualized, genetically-modified
cellular product, for treatment of relapsed or refractory
B-cell precursor acute lymphoblastic leukemia (ALL)
in patients ≤25 years old. The patient's own T cells
are genetically modified to express chimeric antigen
receptors (CAR) and then reinfused. Kymriah is the
first CAR T-cell immunotherapy to become available in
the US. A CAR T-cell product for B-cell non-Hodgkin's
lymphoma is expected to be approved soon.
Idecabtagene Vicleucel (Abecma) for Multiple Myeloma (online only)
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022 (Issue 1663)
. CRS has been successfully
treated with the IL-6 receptor antagonist tocilizumab
(Actemra ...
The FDA has approved idecabtagene vicleucel
(Abecma – BMS), a B-cell maturation antigen (BCMA)-directed genetically-modified cellular product, for
treatment of relapsed or refractory multiple myeloma in
adults who received ≥4 prior lines of therapy, including
a proteasome inhibitor, an immunomodulatory drug,
and an anti-CD38 monoclonal antibody. Abecma is
an individualized cellular product prepared from the
patient’s own T cells, which are genetically modified
to express chimeric antigen receptors (CAR) and
then infused back into the patient. Ciltacabtagene
autoleucel...
Ciltacabtagene Autoleucel (Carvykti) for Multiple Myeloma (online only)
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022 (Issue 1663)
has been successfully treated with the
IL-6 receptor antagonist tocilizumab (Actemra), with
or without corticosteroids ...
The FDA has approved ciltacabtagene autoleucel
(Carvykti – Janssen), a B-cell maturation antigen
(BCMA)-directed genetically-modified cellular product,
for treatment of relapsed or refractory
multiple myeloma in adults who received ≥4 prior
lines of therapy, including a proteasome inhibitor,
an immunomodulatory drug, and an anti-CD38
monoclonal antibody. Carvykti is an individualized
cellular product prepared from the patient's own
T cells, which are genetically modified to express
chimeric antigen receptors (CAR) and then infused
back into the patient. Idecabtagene...