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Table 2 TEAEs that occurred in > 5% of patients overall during the OLE up to and including Week 128 (SAF-OLE population)

From: Long-term evaluation of the safety and efficacy of recombinant human pentraxin-2 (rhPTX-2) in patients with idiopathic pulmonary fibrosis (IPF): an open-label extension study

Preferred term, n (%)

Patients who started rhPTX-2 (n = 37)

Patients who continued rhPTX-2 (n = 74)

Total (n = 111)

Idiopathic pulmonary fibrosis

11 (29.7)

22 (29.7)

33 (29.7)

Dyspnea

6 (16.2)

26 (35.1)

32 (28.8)

Cough

14 (37.8)

16 (21.6)

30 (27.0)

Upper respiratory tract infection

8 (21.6)

18 (24.3)

26 (23.4)

Fatigue

5 (13.5)

14 (18.9)

19 (17.1)

Nasopharyngitis

5 (13.5)

13 (17.6)

18 (16.2)

Diarrhea

2 (5.4)

15 (20.3)

17 (15.3)

Bronchitis

8 (21.6)

8 (10.8)

16 (14.4)

Hypoxia

5 (13.5)

11 (14.9)

16 (14.4)

Arthralgia

4 (10.8)

8 (10.8)

12 (10.8)

Dizziness

2 (5.4)

10 (13.5)

12 (10.8)

Pneumonia

3 (8.1)

9 (12.2)

12 (10.8)

Back pain

3 (8.1)

8 (10.8)

11 (9.9)

Respiratory tract infection

2 (5.4)

9 (12.2)

11 (9.9)

Productive cough

1 (2.7)

9 (12.2)

10 (9.0)

Pulmonary hypertension

4 (10.8)

6 (8.1)

10 (9.0)

Dyspnea exertional

1 (2.7)

8 (10.8)

9 (8.1)

Hypertension

2 (5.4)

6 (8.1)

8 (7.2)

Rash

1 (2.7)

7 (9.5)

8 (7.2)

Blood pressure fluctuation

3 (8.1)

4 (5.4)

7 (6.3)

Gastroesophageal reflux disease

2 (5.4)

5 (6.8)

7 (6.3)

Nausea

1 (2.7)

6 (8.1)

7 (6.3)

Peripheral edema

4 (10.8)

3 (4.1)

7 (6.3)

Headache

1 (2.7)

5 (6.8)

6 (5.4)

Influenza

2 (5.4)

4 (5.4)

6 (5.4)

Pain in extremity

2 (5.4)

4 (5.4)

6 (5.4)

Pyrexia

3 (8.1)

3 (4.1)

6 (5.4)

Sinusitis

3 (8.1)

3 (4.1)

6 (5.4)

  1. OLE, open-label extension; rhPTX-2, recombinant human pentraxin-2; SAF-OLE, Safety Analysis Set of the open-label extension; TEAE, treatment-emergent adverse event
  2. TEAEs were documented according to Medical Dictionary for Regulatory Activities, version 19.0