1 | with relapsed or refractory | | | | | | | 7 | 0.41% |
2 | patients with relapsed or | | | | | | | 6 | 0.35% |
3 | days range 1 to | | | | | | | 6 | 0.35% |
4 | adult patients with relapsed | | | | | | | 6 | 0.35% |
5 | of patients with all | | | | | | | 5 | 0.29% |
6 | is a cd19directed genetically | | | | | | | 5 | 0.29% |
7 | of patients with mcl | | | | | | | 5 | 0.29% |
8 | modified autologous t cell | | | | | | | 5 | 0.29% |
9 | median time to onset | | | | | | | 5 | 0.29% |
10 | the median time to | | | | | | | 4 | 0.24% |
11 | relapsed or refractory mantle | | | | | | | 4 | 0.24% |
12 | immunotherapy indicated for the | | | | | | | 4 | 0.24% |
13 | indicated for the treatment | | | | | | | 4 | 0.24% |
14 | or refractory mantle cell | | | | | | | 4 | 0.24% |
15 | refractory mantle cell lymphoma | | | | | | | 4 | 0.24% |
16 | patients with mcl and | | | | | | | 4 | 0.24% |
17 | days for patients with | | | | | | | 4 | 0.24% |
18 | not resolved by day | | | | | | | 3 | 0.18% |
19 | following treatment with tecartus | | | | | | | 3 | 0.18% |
20 | days with a median | | | | | | | 3 | 0.18% |
21 | overall response rate and | | | | | | | 3 | 0.18% |
22 | cytopenias not resolved by | | | | | | | 3 | 0.18% |
23 | tecartus® brexucabtagene autoleucel is | | | | | | | 3 | 0.18% |
24 | grade 3 or higher | | | | | | | 3 | 0.18% |
25 | for patients with all | | | | | | | 3 | 0.18% |
26 | under accelerated approval based | | | | | | | 3 | 0.18% |
27 | relapsed or refractory bcell | | | | | | | 3 | 0.18% |
28 | or refractory bcell precursor | | | | | | | 3 | 0.18% |
29 | refractory bcell precursor acute | | | | | | | 3 | 0.18% |
30 | days range 2 to | | | | | | | 3 | 0.18% |
31 | brexucabtagene autoleucel is a | | | | | | | 3 | 0.18% |
32 | signs and symptoms of | | | | | | | 3 | 0.18% |
33 | for signs and symptoms | | | | | | | 3 | 0.18% |
34 | accelerated approval based on | | | | | | | 3 | 0.18% |
35 | response rate and durability | | | | | | | 3 | 0.18% |
36 | approved under accelerated approval | | | | | | | 3 | 0.18% |
37 | genetically modified autologous t | | | | | | | 3 | 0.18% |
38 | is approved under accelerated | | | | | | | 3 | 0.18% |
39 | of adult patients with | | | | | | | 3 | 0.18% |
40 | autologous t cell immunotherapy | | | | | | | 3 | 0.18% |