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Table 2 Summary of adverse events incidence, grade and duration by dose level

From: Safety and efficacy of a novel anti-CD19 chimeric antigen receptor T cell product targeting a membrane-proximal domain of CD19 with fast on- and off-rates against non-Hodgkin lymphoma: a first-in-human study

Adverse Event

 

DL-1 (n = 6)

DL-2 (n = 3)

DL-3 (n = 3)

Total (n = 12)

Cytokine Release Syndrome (CRS)

 Any grade

0

1

3

4 (33.3)

  Grade 1/2

0

1

2

3 (25.0)

  Grade ≥ 3

0

0

1

1 (8.3)

 Time to onset, days (range)

-

11

2

6.5 (2–11)

 Time from onset to resolution, days (range)

-

1

1

1 (1–1)

Immune Cell Associated Neurotoxicity Syndrome (ICANS)

 Any grade

1

1

1

3 (25.0)

  Grade 1/2

0

1

1

2 (16.7)

  Grade ≥ 3

1

0

0

1 (8.3)

 Time to onset, days (range)

12

12

8

12 (8–12)

 Time from onset to resolution, days (range)

6

2

3

3 (2–6)

Other Adverse Events AE):

 Total Patients with Grade ≥ 3 AE

4

1

2

7 (58.3)

  Neutropenia

4

1

2

7 (58.3)

  Anemia

3

0

1

4 (33.3)

  Thrombocytopenia

1

0

1

2 (16.7)

  Infection

1

0

1

2 (16.7)

 vAnorexia

0

0

1

1 (8.3)

  Diarrhea

0

0

1

1 (8.3)

  COVID-19

0

1

0

1 (8.3)

  Hypokalemia

0

0

1

1 (8.3)

  Pneumonia

1

0

0

1 (8.3)

  Sepsis

0

0

1

1 (8.3)