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Table 3 Overview of AEs

From: A phase II study of belumosudil for chronic graft-versus-host disease in patients who failed at least one line of systemic therapy in China

AE

Data are n (%) unless stated otherwise

Belumosudil 200 mg once daily (N = 30)

Any AEs

29 (96.7%)

Grade ≥ 3 AEs

11 (36.7%)

Drug-related AEs

19 (63.3%)

SAEs

11 (36.7%)

Drug-related SAEs

4 (13.3%)

AEs leading to dose reduction

1 (3.3%)

AEs leading to dose interruption

2 (6.7%)

AEs leading to treatment discontinuation

5 (16.7%)

AEs leading to death

4 (13.3%)

All-grade TEAEs (≥ 10% of patients)

 Respiratory tract infectiona

14 (46.7%)

 Sinus tachycardia

11 (36.7%)

 Pneumonia

7 (23.3%)

 Hypoproteinemiab

6 (20.0%)

 Hyperuricemia

5 (16.7%)

 Liver injury

5 (16.7%)

 Alanine aminotransferase increased

3 (10.0%)

 Blood creatinine increased

3 (10.0%)

 Blood glucose increased

3 (10.0%)

 Hypertension

3 (10.0%)

 Nausea

3 (10.0%)

 Vomiting

3 (10.0%)

Grade ≥ 3 TEAEs (≥ 5% of patients)

 Pneumonia

5 (16.7%)

  1. AE adverse event, SAE serious adverse event, TEAE treatment-emergent adverse event
  2. aRespiratory tract infection includes AE of upper respiratory tract infection and respiratory tract infection
  3. bHypoproteinemia includes AE of hypoalbuminemia and hypoproteinemia