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Chronic Graft Vs. Host DiseaseNCT05544032

Expanded Access of Axatilimab to Treat a Single Patient With Chronic Graft Versus Host Disease (GVHD)

A study testing axatilimab in people with Chronic Graft Vs. Host Disease, run by Incyte Corporation.

Approved For Marketing

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record

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Trial summary

This program is being offered on a patient by patient basis and will require company, Institutional Review Board/Independent Ethics Committee and Single Patient IND approval. Read more about this study

Who is it for?
Any age
Conditions the study is for
Chronic Graft Vs. Host Disease
What is being tested?
axatilimab
Type of treatment
Injection or infusion
How many people
Not given
Where
No sites listed yet
Study dates
Start not givento not given
Phase
Expanded access

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Child, Adult, Older adult

Who may be able to join

  • -

Who cannot join

  • -

About this study

This program is being offered on a patient by patient basis and will require company, Institutional Review Board/Independent Ethics Committee and Single Patient IND approval.

Being tested
axatilimab
Keywords
Chronic Graft Vs. Host Disease, cGVHD

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • axatilimabDrug

    Also called INCA34176

    Treatment with axatilimab includes receiving intravenous (IV) doses of axatilimab every 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Expanded access
IDs, dates and publications
ClinicalTrials.gov ID
NCT05544032
Sponsor's protocol ID
I-34176-25-07
Status last verified
Jul 2026
First submitted
14 Sep 2022
Last updated
10 Jul 2026
Results posted
No

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