A Study to Evaluate Lanraplenib (LANRA) in Combination With Gilteritinib in Participants With FLT3-mutated Relapsed or Refractory Acute Myeloid Leukemia (AML)
Stopped early · Phase 1/Phase 2
Conditions studied: Acute Myeloid Leukemia, Relapsed Acute Myeloid Leukemia, Refractory Acute Myeloid Leukemia
In brief
The primary objective of this study is to evaluate the safety of lanraplenib (LANRA) in combination with the FMS-like tyrosine kinase 3 (FLT3) inhibitor gilteritinib, in participants with relapsed or refractory (R/R) FLT3-mutated acute myeloid leukemia (AML).
Key facts
- Study ID
- NCT05028751
- Run by
- Kronos Bio
- People needed
- 24
- Starts
- 2022-08-05
- Expected to finish
- 2024-04-09
- Last updated by the study team
- 2024-08-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults ≥18 years of age with acute myeloid leukemia (AML) and at least 1 prior line of therapy
- FMS-like tyrosine kinase 3 (FLT3)-mutated disease documented in a local reference laboratory at the time of consideration for enrollment in the study
- Have the ability to understand the requirements and procedures of the study and sign a written informed consent form
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1 or 2
- Adequate hepatic and renal function
- Prothrombin time (PT), activated partial thromboplastin time (aPTT) and international normalized ratio (INR) ≤1.5x upper limit of normal (ULN) unless receiving therapeutic anticoagulation
- Negative serum ß-human chorionic gonadotropin (HCG) test in women of child-bearing potential (WOCBP)
- Left ventricular ejection fraction ≥50% confirmed by echocardiogram (ECHO) or multi-gated acquisition (MUGA) scan
You may not qualify if…
- Known central nervous system (CNS) involvement with leukemia
- Clinical signs/symptoms of leukostasis that have failed therapy including hydroxyurea and/or leukapheresis of at least 3 days duration
- Pregnant or breastfeeding women
- Active infection with hepatitis B, C or human immunodeficiency virus (HIV) infection
- Disseminated intravascular coagulation with active bleeding or signs of thrombosis
- Known active coronavirus disease 2019 (COVID-19)
- Administration of a live attenuated virus vaccine within 35 days before Cycle 1 Day 1 (C1D1)
- History of non-myeloid malignancy except for the following: adequately treated localized basal cell, or squamous cell carcinoma of the skin, or localized melanoma (with TNM stage either Tis [melanoma in-situ] or T1aN0M0) with complete resection; cervical carcinoma in situ; superficial bladder cancer; asymptomatic prostate cancer without known metastatic disease, with no requirement for therapy or requiring only hormonal therapy and with normal prostate specific antigen for > 1 year prior to start of study therapy; or any other cancer that has been in complete remission without treatment for ≥3 years prior to enrollment
- Clinically significant heart disease
- Prolongation of the long measure between Q wave and T wave in the electrocardiogram (QT) interval at baseline
- Evidence of ongoing uncontrolled systemic bacterial, fungal, or viral infection at the time of study treatment initiation
- Current (within 30 days of study enrollment) drug-induced liver injury, chronic active hepatitis, alcoholic liver disease, nonalcoholic steatohepatitis, primary biliary cholangitis with inadequate response to ursodeoxycholic acid or other health authority approved therapy, extrahepatic obstruction caused by cholelithiasis, cirrhosis of the liver, or portal hypertension
- Ongoing (within 6 weeks of study enrollment) hepatic encephalopathy
- Ongoing immunosuppressive therapy, including systemic chemotherapy for treatment of leukemia
Where it is running
- University of California Los Angeles (UCLA) — Los Angeles, California, United States
- The Blood and Marrow Transplant Group of Georgia — Atlanta, Georgia, United States
- University of Chicago Medical Center — Chicago, Illinois, United States
- Memorial Sloan Kettering Cancer Center — New York, New York, United States
- Oregon Health and Science University — Portland, Oregon, United States
- Texas Oncology - Baylor Charles A. Sammons Cancer Center — Dallas, Texas, United States
- University of Texas MD Anderson Cancer Center — Houston, Texas, United States
- Froedtert Hospital — Milwaukee, Wisconsin, United States
- Hospital Universitario 12 de Octubre — Madrid, Avenida de Córdoba Sin Número, Spain
- Hospital Germans Trias i Pujol — Barcelona, Badalona, Spain
- MD Anderson Cancer Center Madrid — Madrid, Calle de Arturo Soria, Spain
- Hospital Universitari Vall d'Hebrón — Barcelona, Spain
- Institut Català d'Oncologia - Hospital Duran i Reynals (ICO L'Hospitalet) — Barcelona, Spain
- Hospital Clínic de Barcelona — Barcelona, Spain
- Hospital San Pedro de Alcantara — Cáceres, Spain
- Hospital Universitario Fundación Jiménez Díaz — Madrid, Spain
- Hospital Universitari i Politècnic La Fe — Valencia, Spain
Full record on ClinicalTrials.gov
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