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Table 1 Clinical characteristics and baseline data of the participants

From: Efficacy and safety of SHEN26, a novel oral small molecular RdRp inhibitor for COVID-19 treatment: a multicenter, randomized, double-blinded, placebo-controlled, phase II clinical trial

Variables

Placebo group

(n = 24)

200 mg group

(n = 30)

400 mg group

(n = 24)

P1

P2

P3

General information

      

Gender (%)

      

 Male

21 (87.5)

19 (61.3)

16 (66.7)

0.0304

0.0860

0.6810

 Female

3 (12.5)

12 (38.7)

8 (33.3)

 Age (years)

30.4 ± 7.61

35.9 ± 12.50

33.5 ± 10.50

0.0653

0.2502

0.4585

Body weight (kg)

67.75 ± 11.79

67.22 ± 12.97

62.03 ± 10.34

0.8780

0.0807

0.1145

BMI (kg/m2)

23.39 ± 3.09

23.76 ± 3.81

22.18 ± 2.68

0.6999

0.1535

0.0895

Viral load (log10 copies/mL)

7.13 ± 1.02

6.62 ± 1.52

7.41 ± 0.85

0.1665

0.2964

0.0259

COVID-19 severity (%)

      

 Mild

23 (95.8)

31 (100.0)

22 (91.7)

0.2514

0.5510

0.1016

 Moderate

1 (4.2)

0

2 (8.3)

 Severe

0

0

0

History of vaccination (%)

      

 Yes

23 (95.8)

29 (93.5)

22 (91.7)

0.7113

0.5510

0.7898

 No

1 (4.2)

2 (6.5)

2 (8.3)

Time from administration to onset (days)

4.8 ± 0.79

4.5 ± 0.81

5.0 ± 1.38

0.2894

0.4464

0.1106

High risk factors of COVID-19 (%)

   

0.3745

NA

0.3745

 Yes

0

1 (3.2)

0

 No

24 (100.0)

30 (96.8)

24 (100.0)

History of allergy (%)

      

 Yes

2 (8.3)

0

0

0.1016

0.1486

NA

 No

22 (91.7)

31 (100.0)

24 (100.0)

Vaccination within 1 month (%)

      

 Yes

0

0

0

NA

NA

NA

 No

24 (100.0)

31 (100.0)

24 (100.0)

Time since the last COVID-19 vaccination (days)

23

29

22

0.1007

0.3704

0.4946

Attention of the other COVID-19 related clinical trials (%)

   

0.2514

> 0.9999

0.2514

 Yes

1 (4.2)

0

1 (4.2)

 No

23 (95.8)

31 (100.0)

23 (95.8)

  1. P1 = 200 mg group vs. Placebo, P2 = 400 mg group vs. Placebo, P3 = 200 mg group vs. 400 mg group