A phase 3 randomized trial of mavorixafor, a CXCR4 antagonist, for WHIM syndrome

Blood. 2024 Jul 4;144(1):35-45. doi: 10.1182/blood.2023022658.

Abstract

We investigated efficacy and safety of mavorixafor, an oral CXCR4 antagonist, in participants with warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome, a rare immunodeficiency caused by CXCR4 gain-of-function variants. This randomized (1:1), double-blind, placebo-controlled, phase 3 trial enrolled participants aged ≥12 years with WHIM syndrome and absolute neutrophil count (ANC) ≤0.4 × 103/μL. Participants received once-daily mavorixafor or placebo for 52 weeks. The primary end point was time (hours) above ANC threshold ≥0.5 × 103/μL (TATANC; over 24 hours). Secondary end points included TAT absolute lymphocyte count ≥1.0 × 103/μL (TATALC; over 24 hours); absolute changes in white blood cell (WBC), ANC, and absolute lymphocyte count (ALC) from baseline; annualized infection rate; infection duration; and total infection score (combined infection number/severity). In 31 participants (mavorixafor, n = 14; placebo, n = 17), mavorixafor least squares (LS) mean TATANC was 15.0 hours and 2.8 hours for placebo (P < .001). Mavorixafor LS mean TATALC was 15.8 hours and 4.6 hours for placebo (P < .001). Annualized infection rates were 60% lower with mavorixafor vs placebo (LS mean 1.7 vs 4.2; nominal P = .007), and total infection scores were 40% lower (7.4 [95% confidence interval [CI], 1.6-13.2] vs 12.3 [95% CI, 7.2-17.3]). Treatment with mavorixafor reduced infection frequency, severity, duration, and antibiotic use. No discontinuations occurred due to treatment-emergent adverse events (TEAEs); no related serious TEAEs were observed. Overall, mavorixafor treatment demonstrated significant increases in LS mean TATANC and TATALC, reduced infection frequency, severity/duration, and was well tolerated. The trial was registered at www.clinicaltrials.gov as #NCT03995108.

Publication types

  • Randomized Controlled Trial
  • Clinical Trial, Phase III
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aminoquinolines
  • Benzimidazoles
  • Butylamines
  • Child
  • Double-Blind Method
  • Female
  • Humans
  • Immunologic Deficiency Syndromes* / drug therapy
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Primary Immunodeficiency Diseases* / drug therapy
  • Quinolines / administration & dosage
  • Quinolines / adverse effects
  • Quinolines / therapeutic use
  • Receptors, CXCR4* / antagonists & inhibitors
  • Warts* / drug therapy
  • Young Adult

Substances

  • Receptors, CXCR4
  • CXCR4 protein, human
  • mavorixafor
  • Quinolines
  • Aminoquinolines
  • Benzimidazoles
  • Butylamines

Supplementary concepts

  • WHIM syndrome

Associated data

  • ClinicalTrials.gov/NCT03995108