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Table 2 Dosage and application form of concomitant VA treatment during ICM therapy

From: Clinical safety of combined therapy of immune checkpoint inhibitors and Viscum album L. therapy in patients with advanced or metastatic cancer

VA treatment

Number of patients

VA, n (%)

9 (56.3)

 Abnobaviscum, n (%)

7 (43.8)

  Abnobaviscum Fraxini, 0.2 mg, s.c., n (%)

1 (6.3)

  Abnobaviscum Fraxini, 20 mg, i.v., n (%)

1 (6.3)

  Abnobaviscum Fraxini, 40 mg, i.v., n (%)

1 (6.3)

  Abnobaviscum Fraxini, 60 mg, i.v., n (%)

1 (6.3)

  Abnobaviscum Fraxini, 20–60 mg, i.v., n (%)

1 (6.3)

   Abnobaviscum Amygdali, 0.2 mg, s.c. /Abnobaviscum Fraxini, 20–40 mg, i.v., n (%)

2 (12.5)

 Helixor P, 200 mg, i.v., n (%)

1 (6.3)

 Iscador Qu, 5 mg, s.c., n (%)

1 (6.3)

No VA, n (%)

7 (56.3)

  1. VA, Viscum album L.; %, as percent from total patient number n = 16; s.c., subcutaneous; i.v. intravenous