Axatilimab for Sclerotic Chronic Graft-versus-Host Disease

Launched by FRED HUTCHINSON CANCER CENTER · Jun 2, 2025

Keywords

ClinConnect Summary

This clinical trial is studying a treatment called axatilimab for patients with chronic graft-versus-host disease (cGVHD), specifically focusing on those who have skin that has become thickened or hardened due to this condition. cGVHD can occur after receiving a donor stem cell transplant and can lead to serious disabilities, even though it may not increase the risk of death. The trial aims to see if axatilimab can help improve or prevent worsening of the skin symptoms related to cGVHD, as current treatments often come with unwanted side effects and limited success.

To participate in this trial, you need to be at least 18 years old and have received a donor stem cell transplant with active cGVHD that requires treatment. Your skin must show specific signs of thickening, and you should not have received certain other medications recently. Throughout the study, participants will receive axatilimab and will be monitored for how well it works and any side effects. It's important to note that participants who can become pregnant or father a child will need to use effective birth control during the study. This trial is not yet recruiting participants, but it aims to provide new insights into treating this challenging condition.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Adults aged 18 and older
• • Ability to understand and willingness to sign a written informed consent document
• • Allogeneic stem cell transplant, with active cGVHD requiring systemic treatment. Active cGVHD is defined as the presence of signs and symptoms of cGVHD diagnosed per the 2014 National Institutes of Health (NIH) Consensus Development Project on Criteria for Clinical trials in cGVHD
• • Sclerotic skin score 2-3 or PROM \< 24 due to cGVHD
• • Initial diagnosis of sclerosis within the past 24 weeks (168 days)
• • No new non-corticosteroid systemic immunosuppressive agent within 28 days prior to screening, unless there is a plan to stop them no later than 21 days after the first dose of axatilimab. Receipt of systemic corticosteroids ≤ 1 mg/kg prednisone or prednisone equivalent daily is allowed at the time of enrollment and may be continued after axatilimab initiation
• • If patient has been previously treated with systemic immunosuppression for sclerosis, one of the following two conditions must be true: (a) the systemic immunosuppressive treatment(s) were given for at least 60 days and the sclerotic cGVHD either did not respond or progressed; (b) the systemic immunosuppressive treatment(s) were given for less than 60 days due to lack of sclerotic cGVHD response, sclerotic cGVHD progression, toxicity or logistic reasons and have or will be stopped no later than 21 days after the first dose of axatilimab
• • Karnofsky performance status ≥ 60%
• • Absolute neutrophil count ≥ 1.0 x 10\^9/L (evaluated during the 28-day screening period)
• • Platelet count ≥ 50 x 10\^9/L (evaluated during the 28-day screening period) (without transfusion within 2 weeks of study entry)
• • If no suspected or proven liver cGVHD, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 x upper limit of normal (ULN) (evaluated during the 28-day screening period) unless due to Gilbert's disease
• • If no suspected or proven liver cGVHD, total bilirubin ≤ 1.5 x ULN (evaluated during the 28-day screening period) unless due to Gilbert's disease
• • For patients with suspected or documented liver cGVHD, ALT and AST ≤ 5 x ULN (evaluated during the 28-day screening period) unless due to Gilbert's disease
• • For patients with suspected or documented liver cGVHD, total bilirubin ≤ 1.5 x ULN (evaluated during the 28-day screening period) unless due to Gilbert's disease
• • Estimated creatinine clearance ≥ 30 mL/min/1.73m\^2 based on the institutional formula
• • Male and female participants of reproductive potential must be willing to employ highly effective and acceptable forms of contraception from screening through 90 days after the last dose of study treatment.
• • Adolescent and adult male patients capable of fathering a child who are non-sterilized and who are not abstinent and intend to be sexually active with a female partner of childbearing potential must use two methods of birth control from the time of screening throughout the total duration of the study intervention treatment period and 90 days after the last dose of study intervention. Male patients should refrain from sperm donation throughout this period
• • Female patients of childbearing potential who are not abstinent and intend to be sexually active with a non-sterilized male partner must use at least one highly effective method of contraception from the time of screening throughout the total duration of the study intervention treatment period and 90 days after the last dose of study intervention. Periodic abstinence, the rhythm method, and the withdrawal method are not acceptable methods of birth control. Female patients should also refrain from breastfeeding throughout this period
• • Female subjects of childbearing potential must have a negative serum pregnancy test within 72 hours prior to treatment initiation. Females of childbearing potential are defined as sexually mature females without prior hysterectomy or who have had any evidence of menses in the past 12 months. However, females who have been amenorrheic for 12 or more months are still considered to be of childbearing potential if the amenorrhea is possibly due to prior chemotherapy, anti-estrogens, or ovarian suppression
• Exclusion Criteria:
• • Hospitalization for evaluation or management of an infection within 28 days prior to screening
• • History or other evidence of significant organ dysfunction that would make the patient, in the opinion of the investigator, unsuitable for the study
• • On more than 1 mg/kg/day prednisone or prednisone equivalent
• • History of non-compliance
• • History or other evidence of uncontrolled psychiatric illness that that would limit compliance with study requirements
• • Receipt of an investigational agent within 28 days prior to screening
• • Any evidence (histologic, cytogenetic, molecular, hematologic, or mixed) of relapse of the underlying cancer or post-transplant lymphoproliferative disease at the time of screening
• • Diagnosed with another malignancy (other than malignancy for which transplant was performed) within 3 years of study enrollment, unless previously treated with curative intent (e.g. complete resected basal or squamous cell carcinoma of the skin)
• • Active hepatitis B (defined as hepatitis B virus \[HBV\] surface antigen positive and HBV core antibody positive, with positive HBV deoxyribonucleic acid \[DNA\], or HBV positive core antibody alone with positive HBV DNA) or hepatitis C (defined as positive hepatitis C \[HCV\] antibody with positive HCV ribonucleic acid \[RNA\])
• • Suspected active or latent tuberculosis (as confirmed by a positive QuantiFERON® test or other tuberculosis blood test)
• • History of acute or chronic pancreatitis
• • History of myositis
• • Pregnant or breastfeeding
• • Previous exposure to colony stimulating factor 1 receptor (CSF-1R) therapies