Wednesday, July 8, 2026

Drug profile · INN

mavorixafor

mavorixafor (XOLREMDI) is a c-x-c chemokine receptor type 4 antagonist. Route of administration: oral. Current US regulatory status: approved.

FDA: approved EMA: approved Antineoplastic and immunomodulating agents (L03) L03AX24
US status approved
Patents linked 10
Pipeline programs 7
News articles 2
Drug details — mavorixafor

Quick answer

mavorixafor (XOLREMDI) is a c-x-c chemokine receptor type 4 antagonist. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN mavorixafor
Brand XOLREMDI
Mechanism C-X-C chemokine receptor type 4 antagonist
Target C-X-C chemokine receptor type 4
Therapeutic class Antineoplastic and immunomodulating agents (L03)
Route ORAL
Formulation CAPSULE
ATC code L03AX24

Mechanism of action

C-X-C chemokine receptor type 4 antagonist

Primary target: C-X-C chemokine receptor type 4

Approval history

Authority Status Date
FDA approved
EMA approved

Recent coverage

Pipeline programs

  1. Mavorixafor Phase 3 · X4 Pharmaceuticals · Neutropenia
  2. Mavorixafor Phase 3 · X4 Pharmaceuticals · WHIM Syndrome
  3. Mavorixafor, Mavorixafor Placebo Capsules Phase 3 · X4 Pharmaceuticals · Neutropenias
  4. Mavorixafor, Placebo to Test IMP Phase 3 · X4 Pharmaceuticals · WHIM Syndrome
  5. Mavorixafor Phase 1 · X4 Pharmaceuticals · Healthy Participants
  6. Mavorixafor Phase 1 · X4 Pharmaceuticals · Waldenstrom's Macroglobulinemia
  7. Mavorixafor Phase 1 · X4 Pharmaceuticals · Hepatic Insufficiency

Related & competitor drugs

  1. abiraterone acetate Antineoplastic and immunomodulating agents (L02)
  2. anagrelide Antineoplastic and immunomodulating agents (L01)
  3. apremilast Antineoplastic and immunomodulating agents (L04)
  4. arsenic trioxide Antineoplastic and immunomodulating agents (L01)
  5. axitinib Antineoplastic and immunomodulating agents (L01)
  6. azacitidine Antineoplastic and immunomodulating agents (L01)

Related patents

  1. US 12377090

    Methods for treating neutropenia

    Expires Mon Jul 31 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  2. US 12285424

    Methods for treating neutropenia

    Expires Mon Apr 24 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  3. US 12115156

    Compositions of CXCR4 inhibitors and methods of preparation and use

    Expires Mon Oct 10 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  4. US 11357742

    Methods for treating cancer

    Expires Mon Jun 09 2042 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  5. US 11337969

    Methods for treating cancer

    Expires Mon May 19 2042 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  6. US 11219621

    Methods for treating immunodeficiency disease

    Expires Mon Jan 06 2042 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  7. US 11045461

    Compositions of CXCR4 inhibitors and methods of preparation and use

    Expires Mon Jun 24 2041 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  8. US 10953003

    Methods for treating cancer

    Expires Mon Mar 18 2041 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  9. US 10610527

    Methods for treating immunodeficiency disease

    Expires Mon Apr 02 2040 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  10. US 10548889

    Compositions of CXCR4 inhibitors and methods of preparation and use

    Expires Mon Jan 30 2040 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is mavorixafor?

mavorixafor (XOLREMDI) is a c-x-c chemokine receptor type 4 antagonist. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for mavorixafor?

XOLREMDI is a marketed brand name for mavorixafor. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of mavorixafor?

mavorixafor has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.