Table 2 Summary of primary and key secondary efficacy endpoint analyses at week 24.

From: Evaluation of gecacitinib vs hydroxyurea in patients with intermediate-2 or high-risk myelofibrosis: final analysis results from a randomized phase 3 study

 

Gecacitinib

HU

P value

(n = 71)

(n = 34)

SVR35 rate assessed by IRC at week 24, %

64.8

26.5

0.0002

TSS50 rate at week 24, %

62

50

0.2065

Transfusion-dependent to independent, %

16.7

0

0.4386

Non-transfusion-dependent baseline HGB ≤ 100 g/L exhibited a ≥20 g/L HGB increase, %

31

15

0.1827

≥50% Reduction in transfusion frequency, %

63.6

60

>0.9999

≥50% Reduction in transfusion units, %

54.5

40

0.4795

Mean absolute change in HGB at week 24, g/L

1.27

−3.5

NA

Mean absolute change in PLT at week 24, 109/L

−93.28

−182.56

NA

Clinical improvement, %

70.4

41.2

NA

  1. HGB hemoglobin level, PLT platelet count, NA not available.