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NCT03005327 · ClinicalTrials.gov registry record · Phase 2

A Dose Determination and Safety Study of X4P-001 (Mavorixafor) in Participants With Warts, Hypogammaglobulinemia, Infections, and Myelokathexis (WHIM) Syndrome

A Phase 2 study, sponsored by X4 Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
8
Enrollment target

NCT03005327 is a Phase 2 study that has completed, run by X4 Pharmaceuticals. The registered enrollment target is 8 participants.

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The verdict

NCT03005327, a Phase 2 study, has completed, sponsored by X4 Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
8 participants
Enrollment target

Study Summary

This is a Phase 2 study with an initial 24-week Treatment Period and an Extension Phase. The primary objectives of this Phase 2 study are to determine the safety, tolerability, and dose selection of mavorixafor in participants with WHIM syndrome. Participants may continue treatment in an Extension Phase, if regionally applicable, until mavorixafor becomes available via an alternative mechanism (for example, drug is commercially available, an expanded access program, etc.) or until the study is terminated by the Sponsor for any reason.

Interventions

  • DRUG X4P-001

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2016-12
Est. Completion 2022-06-16
Phase Phase 2

Sponsor

X4 Pharmaceuticals

11 total trials

What the Registry Record Tells You About NCT03005327

The ClinicalTrials.gov registry entry for NCT03005327 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is X4 Pharmaceuticals, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which X4P-001 is the first listed.

NCT03005327 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03005327 about?

NCT03005327 is a clinical study titled "A Dose Determination and Safety Study of X4P-001 (Mavorixafor) in Participants With Warts, Hypogammaglobulinemia, Infections, and Myelokathexis (WHIM) Syndrome". This is a Phase 2 study with an initial 24-week Treatment Period and an Extension Phase. The primary objectives of this Phase 2 study are to determine the safety, tolerability, and dose selection of mavorixafor in participants with WHIM syndrome. Participants may continue treatment in an Extension P...

What is the current status of trial NCT03005327?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 8 participants. The study started on 2016-12. Estimated completion is 2022-06-16.

What interventions are being tested in trial NCT03005327?

The interventions under investigation include: X4P-001 (DRUG).

Who is sponsoring clinical trial NCT03005327?

This trial is sponsored by X4 Pharmaceuticals, which has 11 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.