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Table 3 Most frequent TEAEs (> 5% of subjects) in double-blind period up to 12 weeks

From: Efficacy and safety of namilumab, a human monoclonal antibody against granulocyte-macrophage colony-stimulating factor (GM-CSF) ligand in patients with rheumatoid arthritis (RA) with either an inadequate response to background methotrexate therapy or an inadequate response or intolerance to an anti-TNF (tumour necrosis factor) biologic therapy: a randomized, controlled trial

Preferred term

Placebo (N = 27)

Namilumab

20 mg (N = 28)

80 mg (N = 25)

150 mg (N = 28)

Nasopharyngitis

5 (18.5)

5 (17.9)

1 (4.0)

4 (14.3)

Dyspnoea

0

1 (3.6)

2 (8.0)

3 (10.7)

Bronchitis

2 (7.4)

1 (3.6)

1 (4.0)

1 (3.6)

Headache

1 (3.7)

1 (3.6)

3 (12.0)

0

Upper respiratory tract infection

0

0

2 (8.0)

1 (3.6)

Rheumatoid arthritis

0

2 (7.1)

2 (8.0)

0

Hypertension

0

0

0

2 (7.1)

Laryngitis

0

0

2 (8.0)

0

Menorrhagia

0

2 (7.1)

0

0

Urticaria

0

2 (7.1)

0

0

  1. Values are n (%). TEAE treatment-emergent adverse event