Evidence map›Paper›PMID 32870250›Full record

Trial reportBlood2020

Results of a phase 2 trial of an oral CXCR4 antagonist, mavorixafor, for treatment of WHIM syndrome.

David C Dale, Frank Firkin, Audrey Anna Bolyard, Merideth Kelley, Vahagn Makaryan, Kenneth J Gorelick, Tarek Ebrahim, Varun Garg, Weihua Tang, Honghua Jiang and 2 more

Erratum issued Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Blood, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT03005327 (A Phase 2, Open-Label, Multi-Center Trial of Mavorixafor in Patients With WHIM Syndrome), which is not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.9field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03005327 phase2completednot on this map

A Phase 2, Open-Label, Multi-Center Trial of Mavorixafor in Patients With WHIM Syndrome

TypeinterventionalSponsorX4 PharmaceuticalsRan2016 to 2022Enrolled8ConditionsWHIM SyndromeArmsX4P-001
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 67 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. Review
  6. Article
  7. Article
  8. Current infectious disease management challenges in inborn errors of immunity.Annals of clinical microbiology and antimicrobials · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

David C DaleDepartment of Medicine, University of Washington, Seattle, WA.
Frank FirkinDepartment of Medicine and.
Audrey Anna BolyardUniversity of Washington, Severe Chronic Neutropenia International Registry, Seattle, WA; and.
Merideth KelleyDepartment of Medicine, University of Washington, Seattle, WA.
Vahagn MakaryanDepartment of Medicine, University of Washington, Seattle, WA.
Kenneth J GorelickX4 Pharmaceuticals, Inc, Cambridge, MA.
Tarek EbrahimX4 Pharmaceuticals, Inc, Cambridge, MA.
Varun GargX4 Pharmaceuticals, Inc, Cambridge, MA.
Weihua TangX4 Pharmaceuticals, Inc, Cambridge, MA.
Honghua JiangX4 Pharmaceuticals, Inc, Cambridge, MA.
Renato SkerljX4 Pharmaceuticals, Inc, Cambridge, MA.
Sarah Beaussant CohenX4 Pharmaceuticals, Inc, Cambridge, MA.
University of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome is a rare primary immunodeficiency caused by gain-of-function mutations in the CXCR4 gene. We report the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy of mavorixafor from a phase 2 open-label dose-escalation and extension study in 8 adult patients with genetically confirmed WHIM syndrome. Mavorixafor is an oral small molecule selective antagonist of the CXCR4 receptor that increases mobilization and trafficking of white blood cells from the bone marrow. Patients received escalating doses of mavorixafor, up to 400 mg once daily. Five patients continued on the extension study for up to 28.6 months. Mavorixafor was well tolerated with no treatment-related serious adverse events. At a median follow-up of 16.5 months, we observed dose-dependent increases in absolute neutrophil count (ANC) and absolute lymphocyte count (ALC). At doses ≥300 mg/d, ANC was maintained at >500 cells per microliter for a median of 12.6 hours, and ALC was maintained at >1000 cells per microliter for up to 16.9 hours. Continued follow-up on the extension study resulted in a yearly infection rate that decreased from 4.63 events (95% confidence interval, 3.3-6.3) in the 12 months prior to the trial to 2.27 events (95% confidence interval, 1.4-3.5) for patients on effective doses. We observed an average 75% reduction in the number of cutaneous warts. This study demonstrates that mavorixafor, 400 mg once daily, mobilizes neutrophil and lymphocytes in adult patients with WHIM syndrome and provides preliminary evidence of clinical benefit for patients on long-term therapy. The trial was registered at www.clinicaltrials.gov as #NCT03005327.

Indexed as

Administration, OralAdolescentAdultAminoquinolinesBenzimidazolesButylaminesFemaleHumansLeukocyte CountMaleMiddle AgedNeutrophilsPrimary Immunodeficiency DiseasesProspective StudiesReceptors, CXCR4WartsAminoquinolinesBenzimidazolesButylaminesCXCR4 protein, humanmavorixaforReceptors, CXCR4

Identifiers

PMID32870250
PMCPMC7770568
OpenAlexW3082684961

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.