MedPath

A Study of ARGX-110 in Combination With Azacytidine in Participants With Newly Diagnosed Acute Myeloid Leukemia (AML) or High Risk Myelodysplatic Syndrome (MDS)

Phase 1
Completed
Conditions
Leukemia, Myeloid, Acute
Myelodysplastic Syndromes
Interventions
Registration Number
NCT03030612
Lead Sponsor
OncoVerity, Inc.
Brief Summary

The purpose of this study is to determine the maximum tolerated dose (MTD) of ARGX-110 and/or the recommended Phase II dose (RP2D) in combination with a standard dose of azacytidine (AZA) in Phase 1; and to evaluate efficacy of ARGX-110 when administered at a RP2D level established in Phase I in combination with a standard dose of AZA (proof-of concept) by evaluating overall response rate (ORR) in Phase 2.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
38
Inclusion Criteria
  • Signed informed consent form (ICF) indicating an understanding of the purposes, risks, and procedures required for the study and willingness and ability to participate in the study
  • Acute myeloid leukemia (AML) or high risk myelodysplastic syndrome (MDS) (according to 2016 World Health Organization [WHO] classification definition of greater than or equal to [>=] 20 percent [%] blasts) (bone marrow) unsuitable for intensive treatment (including stem cell transplantation) with a curative intent, but eligible to receive azacytidine (AZA) treatment
  • Expected life expectancy >= 3 months, at the discretion of the investigator
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
  • Women of childbearing potential having a negative serum pregnancy test at screening and within 48 hours before infusion of ARGX-110 on Day -14, and willing to use an effective contraceptive method (intrauterine devices, hormonal contraceptives, contraceptive pill, implants, transdermal patches, hormonal vaginal devices, infusions with prolonged release) during the study and for at least 3 months after the last study drug administration
Exclusion Criteria
  • Prior or concurrent malignancy, except for the following: (1) adequately treated basal cell or squamous cell skin cancer; (2) carcinoma in situ of the cervix; (3) carcinoma in situ of the breast; (4) incidental histological finding of Prostate cancer (Tumour, Node, Metastasis [TNM] stage T1a or T1b), or; (5) Any other cancer from which the subject has been disease-free for more than 2 years
  • Any previous AML or MDS chemo- or radiotherapy (with the exception of hydroxyurea/Litalir for leukocyte control which should be discontinued by the first day of AZA, local radiation therapy, therapy for basal or squamous cell carcinoma of the skin)
  • Treatment with any investigational product within 4 weeks before the first administration of ARGX-110
  • Any known active or chronic infection, including human immunodeficiency virus (HIV) and hepatitis B or C virus infection
  • Any other concurrent disease or medical condition that is likely to interfere with study procedures or results, or that in the opinion of the investigator would constitute a hazard for participating in this study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
ARGX-110 with Azacytidine (AZA)AZAPhase 1: Participants will receive loading dose of ARGX-110 1 milligram per kilogram (mg/kg) body weight (cohort 1), 3 mg/kg body weight (cohort 2), 10 mg/kg body weight (cohort 3) or 20 mg/kg body weight (cohort 4) administered intravenously (IV) in combination with AZA standard dose of 75 milligram per meter square (mg/m\^2) body surface area (BSA) administered subcutaneously (SC) / intravenously (IV). Phase 2: Participants will receive loading dose of ARGX-110 IV at a recommended dose for Phase 2 (RP2D) level from phase 1 in combination with AZA standard dose of 75 mg/m\^2 BSA, administered SC/IV as per local practice.
ARGX-110 with Azacytidine (AZA)ARGX-110Phase 1: Participants will receive loading dose of ARGX-110 1 milligram per kilogram (mg/kg) body weight (cohort 1), 3 mg/kg body weight (cohort 2), 10 mg/kg body weight (cohort 3) or 20 mg/kg body weight (cohort 4) administered intravenously (IV) in combination with AZA standard dose of 75 milligram per meter square (mg/m\^2) body surface area (BSA) administered subcutaneously (SC) / intravenously (IV). Phase 2: Participants will receive loading dose of ARGX-110 IV at a recommended dose for Phase 2 (RP2D) level from phase 1 in combination with AZA standard dose of 75 mg/m\^2 BSA, administered SC/IV as per local practice.
Primary Outcome Measures
NameTimeMethod
Phase 2: Overall Response Rate (ORR)Up to 3.6 years

ORR is defined as the sum of Complete remission (CR), CR with incomplete recovery (CRi), morphologic leukemia-free state (MLFS), partial remission (PR) at the ARGX-110 RP2D level that was established in Phase 1 according to established response criteria for Acute myeloid leukemia (AML).

Phase 1: Number of Participants with Dose Limiting Toxicity (DLT)Up to 3.6 years

DLTs will be defined as any of the following drug-related events: Any grade 3 or higher drug related non-hematological toxicity or; Grade 3 or higher IRRs or; inability to administer the next dose due to a drug-related adverse event or a delay of the administration of the next dose due to toxicities for more than 14 days despite adequate medication or; drug-related grade 4 febrile neutropenia or; drug-related grade 4 anemia which cannot be adequately treated.

Secondary Outcome Measures
NameTimeMethod
Phase 1 and Phase 2: Area Under the Serum Concentration-Time Curve from Time Zero to Infinite (AUC[0-infinity]) of ARGX-110Up to 3.6 years

AUC(0-infinity) is defined as area under the serum analyte concentration-time curve from time 0 to infinite time of ARGX-110.

Phase 1 and Phase 2: Elimination Half-Life (t1/2) of ARGX-110Up to 3.6 years

t1/2 is defined as the time measured for the serum concentration to decrease by 1 half of its original concentration.

Phase 1 and Phase 2: Number of Participants with Minimal Residual Disease (MRD) to ARGX-110Up to 3.6 years

Minimal residual disease assessments will be performed on bone marrow aspirates and/or whole blood by flow cytometry.

Phase 1 and Phase 2: Time to ResponseUp to 3.6 years

Time to response is defined as response measured from the time from first dose of study drug to date of response (CR, CRi, MLFS, PR).

Phase 1 and Phase 2: Number of Participants Achieving Transfusion Independence (TI)Up to 3.6 years

Number of participants reaching greater than or equal to (\>=) 8 consecutive weeks without red blood cell (RBC-TI) and/or platelet (PLT-TI) transfusion. The first day of the \>=8-week period with no transfusions is noted as the time at which participants first achieved TI.

Phase 1 and Phase 2: Number of Participants with Adverse EventsUp to 3.6 years

An AE is any untoward medical event that occurs in a participant administered an investigational product, and it does not necessarily indicate only events with clear causal relationship with the relevant investigational product.

Phase 1 and Phase 2: Trough Concentration (Ctrough) of ARGX-110Up to 3.6 years

Ctrough is defined as the observed serum concentration before dosing or at the end of the dosing interval.

Phase 1 and Phase 2: Maximum Observed Concentration (Cmax) of ARGX-110Up to 3.6 years

Cmax is the maximum observed concentration.

Biomarker Assessment of ARGX-110Up to 3.6 years

Biomarkers including CD70 and CD27 assessment will be performed on bone marrow aspirates and/or whole blood.

Phase 1 and Phase 2: Number of Participants with Anti-drug Antibodies (ADA) to ARGX-110Up to 3.6 years

Venous blood samples and bone marrow aspirate will be used to evaluate presence of anti-drug antibodies to ARGX-110. Participants with titer of confirmed positive samples for ARGX-110 antibodies will be reported.

Phase 1 and Phase 2: Number of Participants with Complete Remission (CR)Up to 3.6 years

Complete remission is defined as number of participants who have bone marrow blasts less than (\<) 5 percent (%); absence of blasts with Auer rods; absence of extramedullary disease; absolute neutrophil count greater than (\>) 1.0 \* 10\^9 per liter (L) (1000 per microliter \[µL\]); platelet count \> 100 \* 10\^9/L (100.000/mc); independence of red cell transfusions.

Phase 1 and Phase 2: Area Under the Serum Concentration-Time Curve During the Dosing Interval (AUCtau)Up to 3.6 years

AUCtau is the area under the serum concentration-time curve during the dosing interval.

Phase 1 and Phase 2: Apparent Volume of Distribution (Vd/F) of ARGX-110Up to 3.6 years

Vd/F is defined as Dose/\[Lambda (z)\*AUC (0-infinity)\].

Phase 1 and Phase 2: Number of Participants with CR with Incomplete Recovery (CRi)Up to 3.6 years

CRi is defined as number of participants who have all CR criteria except for residual neutropenia (\< 1.0 \* 10\^9/L \[1000/mc\]) or thrombocytopenia (\< 100 \* 10\^9/L \[100.000/mc\]).

Phase 1 and Phase 2: Number of Participants with Morphologic Leukemia-free State (MLFS)Up to 3.6 years

MLFS is defined as number of participants who have bone marrow blasts \< 5%; absence of blasts with Auer rods; absence of extramedullary disease; no hematologic recovery required.

Phase 1 and Phase 2: Number of Participants with Partial remission (PR)Up to 3.6 years

PR is defined as number of participants who have all hematologic criteria of CR; decrease of bone marrow blast percentage to 5% to 25%; and decrease of pretreatment bone marrow blast percentage by at least 50%.

Phase 1 and Phase 2: Overall Survival (OS)Up to 3.6 years

OS is defined as death from any cause; measured from the date of first dose to the date of death from any cause.

Phase 1 and Phase 2: Total Systemic Clearance (CL) of ARGX-110Up to 3.6 years

CL is the total systemic clearance of drug after intravenous (IV) administration.

Phase 1 and Phase 2: Time to Neutrophil RecoveryUp to 3.6 years

Time to neutrophil recovery will be calculated from number of days from Day 1 of commencing study treatment to first day neutrophils 0.5 \* 10\^9 per liter or 1.0 \* 10\^9 per liter.

Phase 1: Levels of B CellsUp to 3.6 years

Levels of B cells will be reported.

Phase 1: Levels of NK CellsUp to 3.6 years

Levels of NK cells will be reported.

Phase 1 and Phase 2: Number of Participants with 30 Day and 60 Day Mortality30 and/or 60 days after the first administration

Number of participants with 30 Day and 60 Day Mortality will be reported.

Phase 1 and Phase 2: Time to Transfusion IndependenceUp to 3.6 years

Time until TI for RBC and/or PLT will be measured from the date of entry into a study to the first day of the 8-weeks period with no transfusions.

Phase 1 and Phase 2: Duration of Transfusion IndependenceUp to 3.6 years

Time between the last transfusion before the start of the TI period and the first transfusion after the start of the TI period, which occurred \>=8 weeks later.

Phase 1: Levels of T, B and NK CellsUp to 3.6 years

Levels of T, B and NK cells will be reported by immunophenotyping (performed by flow cytometry or mass cytometry). .

Phase 1 and Phase 2: Duration of ResponseUp to 3.6 years

Duration of response is defined as the date of achievement of a response (CR, CRi, MLFS, PR) until the date of relapse.

Phase 1 and Phase 2: Relapse-Free Survival (RFS)Up to 3.6 years

RFS is defined as disease relapse or participant death from any cause; measured from the date of achievement of a remission (CR, CRi) until the date of relapse or death from any cause.

Phase 1 and Phase 2: Time to Platelet RecoveryUp to 3.6 years

Time to platelet recovery will be calculated from number of days from day 1 of commencing study treatment to first day neutrophils 50 \* 10\^9 per liter or 100 \* 10\^9 per liter.

© Copyright 2025. All Rights Reserved by MedPath