Table 1 Baseline characteristics of participants in the modified full-analysis cohort

From: Heterologous AD5-nCOV plus CoronaVac versus homologous CoronaVac vaccination: a randomized phase 4 trial

 

Group A (two doses primed + Convidecia, n = 96)

Group B (two doses primed + CoronaVac, n = 102)

Group C (one dose primed + Convidecia, n = 51)

Group D (one dose primed + CoronaVac, n = 50)

Age in years (%)

 18–50

67 (69.8)

69 (67.7)

37 (72.6)

39 (78.0)

 51–59

29 (30.2)

33 (32.4)

14 (27.5)

11 (22.0)

 Median age (IQR)

47.0 (40.3, 51.0)

47.0 (41.0, 52.0)

47.0 (35.0, 51.0)

43.5 (38.5, 49.3)

Sex (%)

 Male

58 (60.4)

64 (62.8)

27 (52.9)

30 (60.0)

 Female

38 (39.6)

38 (37.3)

24 (47.1)

20 (40.0)

Baseline neutralizing antibody against SARS-CoV-2 (%)a

 Negative

70 (72.9)

90 (88.2)

48 (94.1)

48 (96.0)

 Positive

26 (27.1)

12 (11.8)

3 (5.9)

2 (4.0)

Ethnicity

 Han

96 (100)

102 (100)

51 (100)

50 (100)

Time since the last priming dose of inactivated vaccine (months)

 Median (IQR)

3.2 (3.2, 4.6)

3.3 (3.2, 4.6)

1.8 (1.8, 1.8)

1.8 (1.8, 1.8)

Pre-existing AD5-neutralizing antibodies (%)

 Participants with titer ≤ 1:200

27 (28.1)

38 (37.3)

19 (37.3)

15 (30.0)

 Participants with titer > 1:200

69 (71.9)

64 (62.7)

32 (62.7)

35 (70.0)

  1. Data are n (%) or mean ± s.d. or median (IQR). The analysis was based on the modified full-analysis cohort, with some participants reclassified into the correct groups according to the vaccines that they actually received. aSeropositivity for neutralizing antibody against SARS-CoV-2 before receiving a booster vaccination at day 0 is defined as a detectable neutralizing antibody titer ≥ 1:4.