CX-01 Combined With Azacitidine in the Treatment of Relapsed or Refractory Myelodysplastic Syndrome and Acute Myeloid Leukemia

Acute Myeloid Leukemia Clinical Trial

Official title:

A Pilot Study of CX-01 Combined With Azacitidine in the Treatment of Relapsed or Refractory Myelodysplastic Syndrome and Acute Myeloid Leukemia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02995655
• Other study ID #: 201608032
• Secondary ID: CNTX-CX-01-2016-
• Status: Completed
• Phase: Phase 1
• Start date: April 7, 2017
• Est. completion date: April 29, 2019

Study information

• Verified date: December 2019
• Source: Washington University School of Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators hypothesize that CX-01 will disrupt the bone marrow microenvironment and increase the cytotoxic effects of azacitidine on myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) hematopoietic stem cells by disrupting the High-mobility group box protein 1 (HMGB1) interaction with toll-like receptor 4 (TLR4) and receptors for advanced glycation end products (RAGE), the CXC chemokine CXCL12/chemokine receptor 4 (CXCR4) axis, and by disrupting other leukocyte and vascular adhesion molecules. In addition, CX-01 may also help promote count recovery after treatment given its affinity for platelet factor-4 (PF4).

The selection of CX-01 dose for study in relapsed or refractory MDS and AML has been based upon the dual requirements to have sufficient drug administered to have potential activity but without clinically significant anticoagulation. The study dose chosen (4 mg/kg bolus followed by 0.25 mg/kg/hour) fulfills both of these criteria. In addition, this dose is expected to result in serum levels of CX-01 which are significantly higher than the IC90 identified in preclinical studies for inhibition of HMGB1-RAGE, toll-like receptor 2 (TLR2) and TLR4 interaction. Therefore, the chosen dose represents a rational balance between effective dosing and safety in thrombocytopenic patients with MDS and AML. This dose was previously established to be safe and tolerable when combined with cytarabine and idarubicin in patients with AML.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: April 29, 2019
• Est. primary completion date: September 13, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• One of the following diagnoses:

• MDS with International Prostate Symptom Score (IPSS) score of INT-1 or higher and one of the following:

• Symptomatic anemia with either hemoglobin < 10.0 g/dL or requiring red blood cell (RBC) transfusion

• Thrombocytopenia with a history of two or more platelet counts < 50,000/µL or a significant hemorrhage requiring platelet transfusions

• Neutropenia with two or more absolute neutrophil count (ANC) < 1,000/µL

• Non-M3 AML

• Prior treatment with = 4 cycles of a hypomethylating agent (decitabine or azacitidine) without response OR documented disease progression on or after hypomethylating agent therapy

• Age = 18 years old

• Adequate renal and hepatic function defined as all of the following:

• total bilirubin = 1.5 x upper limit of normal (ULN), except in cases of Gilbert's disease

• aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 2.5 x ULN

• serum creatinine < 2.0 x ULN

• Peripheral blood blast count < 10,000/ µL.

• Eastern Cooperative Oncology Group (ECOG) performance status = 2

• Females must be surgically or biologically sterile or postmenopausal or, if of childbearing potential, must agree to use an adequate method of contraception during the study until 30 days after the last treatment. Males must be surgically or biologically sterile or agree to use an adequate method of contraception during the study until 30 days after the last treatment.

• Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

Exclusion Criteria:

• Prior allogeneic stem cell transplant

• Central nervous system (CNS) leukemia

• Diagnosed with AML and eligible for standard induction chemotherapy or stem cell transplantation.

• At an increased risk of hemorrhage.

• Known allergies, hypersensitivity, or intolerance to any form of heparin or azacitidine

• Presence of significant active bleeding or condition requiring maintenance of a platelet count > 50,000/µL

• Presence of any condition requiring any form of anticoagulant therapy (heparin flushes for IV catheter are permitted)

• Receiving concomitant chemotherapy, radiation therapy, or immunotherapy during the duration of treatment on protocol, or within 21 days prior to enrollment

• Known seropositivity for or active viral infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV). Patients who are seropositive because of hepatitis B virus vaccine are eligible.

• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia

• Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 28 days of study entry.

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• AML
• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute
• MDS
• Myelodysplastic Syndromes
• Preleukemia
• Syndrome

Intervention

Drug:
• CX-01
CX-01 at a dose of 4mg/kg on Day 1 of each 28-day cycle, followed by a continuous intravenous infusion at a dose of 0.25 mg/kg/hour for Days 1 through 7 of each cycle.
• Azacitidine
Azacitidine at a dose of 75mg/m^2 on Days 1-7 of each 28-day cycle.

Procedure:
• Bone marrow biopsy
-Baseline, day 28 of even-numbered cycle through Cycle 6, and end of study
• Peripheral blood draw
-Day 1 of each cycle, day 3 of each cycle, day 7 of each cycle, day 28 of every even-numbered cycle through Cycle 6, and end of study

Locations

Country	Name	City	State
United States	Washington University School of Medicine	Saint Louis	Missouri

Sponsors (2)

Lead Sponsor	Collaborator
Washington University School of Medicine	Cantex Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall response rate (partial response or higher)	Overall response rate = the percentage of patients obtaining partial response or higher; Patients will be assessed for response according to modified International Working Group (IWG) criteria	30 days following completion of treatment (estimated to be 28 weeks)
Secondary	Progression-free survival (PFS)	The interval from the date of first dose of study drug to disease progression or death.; Described by median time-to-event and a 95% confidence interval, if estimable, using Kaplan-Meier models	Up to 5 years
Secondary	Disease-free survival (DFS)	The interval from the date of first documentation of a CR to date of recurrence or death. This is determined only for patients achieving a CR; Described by median time-to-event and a 95% confidence interval, if estimable, using Kaplan-Meier models	Up to 5 years
Secondary	Overall survival (OS)	The date of first dose of study drug to the date of death from any cause.; Described by median time-to-event and a 95% confidence interval, if estimable, using Kaplan-Meier models	Up to 5 years
Secondary	Safety and tolerability of regimen as measured by adverse events tabulated by patient	-The descriptions and grading scales found in the revised NCI Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 will be utilized for all toxicity reporting.	30 days following completion of therapy (estimated to be 28 weeks)

External Links

•   Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine