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

NCT ID: NCT02995655

Last Updated: 2019-12-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-04-07
• Study Completion Date: 2019-04-29

Brief 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.

Conditions

Myelodysplastic Syndromes; Acute Myeloid Leukemia; AML; MDS

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

CX-01 + Azacitidine

• CX-01 will be administered as a 5-minute bolus infusion 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. The dose of CX-01 should be calculated based on actual body weight (kg) as measured on Day 1 of each cycle.
• Azacitidine will be administered as a 15-minute intravenous infusion at a dose of 75mg/m^2 on Days 1-7 of each 28-day cycle. Azacitidine dose should be calculated based on actual body weight and height to determine BSA. CX-01 may be administered before or after azacitidine, at the discretion of the treating physician.
• Up to 6 cycles of treatment allowed

Group Type: EXPERIMENTAL

CX-01

Intervention Type: DRUG

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

Intervention Type: DRUG

Azacitidine at a dose of 75mg/m\^2 on Days 1-7 of each 28-day cycle.

Bone marrow biopsy

Intervention Type: PROCEDURE

-Baseline, day 28 of even-numbered cycle through Cycle 6, and end of study

Peripheral blood draw

Intervention Type: PROCEDURE

-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

Interventions

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.

Intervention Type: DRUG

Azacitidine

Azacitidine at a dose of 75mg/m\^2 on Days 1-7 of each 28-day cycle.

Intervention Type: DRUG

Bone marrow biopsy

-Baseline, day 28 of even-numbered cycle through Cycle 6, and end of study

Intervention Type: PROCEDURE

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

Intervention Type: PROCEDURE

Other Intervention Names

2-O, 3-O desulfated heparin; ODSH; Vidaza®; Ladakamycin

Eligibility Criteria

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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cantex Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

Washington University School of Medicine

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Peter Westervelt, M.D., Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Washington University School of Medicine

Locations

Washington University School of Medicine

St Louis, Missouri, United States

Countries

United States

Related Links

http://www.siteman.wustl.edu

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

Other Identifiers

CNTX-CX-01-2016-MDS-1

Identifier Type: OTHER

Identifier Source: secondary_id

201608032

Identifier Type: -

Identifier Source: org_study_id