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Clinical Trial 21114

Cancer Type: Malignant Hematology
Study Type: Treatment
NCT#: NCT04710576

Phase: Phase II
Principal Investigator: Khimani, Farhad

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Study Title

AGAVE-201, A Phase 2, Open-label, Randomized, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of Axatilimab at 3 Different Doses in Patients with Recurrent or Refractory Active Chronic Graft Versus Host Disease who have Received at least 2 Lines of Systemic Therapy


This is a Phase 2 study to evaluate the efficacy, safety, and tolerability of axatilimab at 3 different dose levels in participants with recurrent or refractory active chronic graft versus host disease (cGVHD) who have received at least 2 prior lines of systemic therapy.


Primary: To evaluate the overall response rate (ORR) of axatilimab at 0.3 mg/kg IV Q2W, 1 mg/kg IV Q2W, and 3 mg/kg IV Q4W in patients with cGVHD after failure of least 2 prior lines of therapy. Secondary: To evaluate key secondary measures of clinical benefit; To evaluate secondary measures of clinical benefit; To evaluate the safety and tolerability of axatilimab in patients with cGVHD; Bone morphology; To assess the plasma population PK (pop PK) profile of axatilimab in patients with cGVHD; To assess pharmacodynamic profile of axatilimab; To determine or assess the changes in monocyte level with response; To determine or assess the baseline in monocyte level with response; Immunogenicity



Therapy (NOS)


Axatilimab ()

Inclusion Criteria

Inclusion Criteria:

  • Participants who are allogeneic hematopoietic stem cell transplantation (HSCT) recipients with active cGVHD requiring systemic immune suppression. Active cGVHD is defined as the presence of signs and symptoms of cGVHD per 2014 NIH Consensus Development Project on Criteria for Clinical trials in cGVHD.
  • Participants with refractory or recurrent active cGVHD despite at least 2 lines of systemic therapy. Refractory disease defined as meeting any of the following criteria: The development of 1 or more new sites of disease while being treated for cGVHD. Progression of existing sites of disease despite at least 1 month of standard or investigation therapy for cGVHD. Participants who have not achieved a response within 3 months on their prior therapy for cGVHD and for whom the treating physician believes a new systemic therapy is required. Recurrent cGVHD is active, symptomatic disease (after an initial response to prior therapy) as defined, based on the NIH 2014 consensus criteria, by organ-specific or global assessment or for which the physician believes that a new line of systemic therapy is required.
  • Participants may have persistent, active acute and cGVHD manifestations (overlap syndrome), as defined by 2014 NIH Consensus Development Project on Criteria for Clinical trials in cGVHD.
  • Karnofsky Performance Scale of >60 (if aged 16 years or older); Lansky Performance Score of >60 (if aged > Adequate organ and bone marrow functions evaluated during the 14 days prior to randomization.
  • Creatinine clearance (CrCl) >30 milliliter/minute/1.73 square meter based on the Cockcroft-Gault formula in adult participants and Schwartz formula in pediatric participants.
  • Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
  • Concomitant use a of systemic corticosteroid is allowed but not required. Topical and inhaled corticosteroid agents are allowed. If a participant is taking corticosteroids at study randomization, they must be on a stable dose of corticosteroids for at least 2 weeks prior to Cycle 1 Day 1.
  • Concomitant use of CNI or sirolimus is allowed but not required.
  • Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and protocol.

  • Exclusion Criteria

    Exclusion Criteria:

  • Has acute GVHD without manifestations of cGVHD.
  • Any evidence (histologic, cytogenetic, molecular, hematologic, or mixed) of relapse of the underlying cancer or post-transplant lymphoproliferative disease at the time of screening.
  • History of acute or chronic pancreatitis.
  • History of myositis.
  • History or other evidence of severe illness, uncontrolled infection, allergy to excipients, or any other conditions that would make the participant, in the opinion of the Investigator, unsuitable for the study.
  • Participants with acquired immune deficiency syndrome (AIDS).
  • 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. Hepatitis C (defined as positive hepatitis C [HCV] antibody with positive HCV ribonucleic acid [RNA]).
  • Diagnosed with another malignancy (other than malignancy for which transplant was performed) within 3 years of randomization, unless previously treated with curative intent and approved by Sponsor's Medical Monitor (for example, completely resected basal cell or squamous cell carcinoma of the skin, resected in situ cervical malignancy, resected breast ductal carcinoma in situ, or low-risk prostate cancer after curative resection).
  • Female participant who is pregnant or breastfeeding.
  • Previous exposure to CSF1-R targeted therapies.
  • Taking agents for treatment of cGVHD other than corticosteroids or either a CNI or mTOR inhibitor is prohibited.
  • For approved or commonly used agents, other than corticosteroids, CNI and mTOR inhibitor, a washout of 2 weeks or 5 half-lives, whichever is shorter, is required at study enrollment.
  • Receiving another investigational treatment within 28 days of randomization.
  • Participants should not be participating in any other interventional study.
  • Participants with a of history of latent or active TB before screening; signs or symptoms suggestive of active TB upon medical history and/or physical examination; recent close contact with a person with active TB; positive QuantiFeron TB test at screening.

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