ABC294640 in Treating Patients With Advanced Solid Tumors (ABC-101)

A Phase I, Open-label, Dose-Escalation, Safety, Pharmacokinetic and Pharmacodynamic Study of ABC294640 in Patients With Advanced Solid Tumors

This phase I trial studies the side effects and best dose of ABC294640 in treating patients with advanced solid tumors. ABC294640 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Please note that the FDA OOPD is participating as a funding source.

Study Overview

• Status: Completed
• Conditions: Pancreatic Cancer; Unspecified Adult Solid Tumor, Protocol Specific
• Intervention / Treatment: Drug: sphingosine kinase-2 inhibitor ABC294640

Detailed Description

PRIMARY OBJECTIVES:

I. To assess safety and determine the maximum tolerated dose (MTD) and the dose limiting toxicities (DLT) of ABC294640 (sphingosine kinase-2 inhibitor ABC294640) in patients with solid organ tumors. (Part I) II. To assess the safety and tolerability of ABC294640 at the MTD in an expanded cohort of hepatocellular carcinoma (HCC) patients. (Part II)

SECONDARY OBJECTIVES:

I. To establish the dose of ABC294640 recommended for future phase II protocols. (Part I) II. To describe the pharmacokinetics of ABC294640 in patients with solid organ tumors. (Part I) III. To describe the effects of ABC294640 on plasma levels of sphingosine 1-phosphate in patients with solid organ tumors. (Part I) IV. To assess antitumor activity of ABC294640 in patients with solid organ tumors by objective radiographic assessment using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria. (Part I) V. To describe the pharmacokinetics of ABC294640 in HCC patients. (Part II) VI. To describe the effects of ABC294640 on plasma levels of sphingosine 1-phosphate in HCC patients. (Part II) VII. To assess antitumor activity of ABC294640 in HCC patients by objective radiographic assessment using RECIST 1.1 criteria. (Part II)

OUTLINE: This is a dose-escalation study.

Patients receive sphingosine kinase-2 inhibitor ABC294640 orally (PO) twice daily (BID) on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up monthly for 1 year.

• Study Type: Interventional
• Enrollment (Actual): 22
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • South Carolina
    • Charleston, South Carolina, United States, 29425
      • Medical University of South Carolina

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• PART I:
• Patients with histologically confirmed solid organ carcinomas
• Tumor progression after receiving standard/approved chemotherapy or as first-line therapy for malignancies where there is no standard therapy
• One or more tumors measurable on computed tomography (CT) scan per RECIST 1.1
• Eastern Cooperative Oncology Group (ECOG) performance status =< 2
• Life expectancy of at least 3 months
• Age > 18 years
• Signed, written Institutional Review Board (IRB)-approved informed consent
• A negative pregnancy test (if female)
• Acceptable liver function:
• Bilirubin =< 3 times upper limit of normal (ULN) (Common Terminology Criteria for Adverse Events [CTCAE] Grade 2 baseline)
• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]), alanine aminotransferase (ALT) (serum glutamic pyruvate transaminase [SGPT]) =< 3 x ULN (CTCAE Grade 1 baseline)
• Serum creatinine =< 1.5 X ULN (CTCAE Grade 1 baseline)
• Absolute neutrophil count >= 1000 cells/mm^3
• Acceptable hematologic status:
• Absolute neutrophil coun > 1000 cells/mm3
• Platelet count >= 75,000 (plt/mm^3) (CTCAE Grade 1 baseline)
• Hemoglobin >= 9 g/dL
• Acceptable blood sugar control:
• Fasting glucose value < 160 mg/dL (CTCAE Grade 1 baseline)
• Urinalysis: No clinically significant abnormalities
• Prothrombin time (PT) and partial thromboplastin time (PTT) =< 1.5 X ULN after correction of nutritional deficiencies that may contribute to prolonged PT/PTT
• For men and women of child-producing potential, willingness to use of effective contraceptive methods during the study; if female (or female partner of male subject), is either not of childbearing potential (defined as postmenopausal for >= 1 year or surgically sterile [bilateral tubal ligation, bilateral oophorectomy or hysterectomy]) or practicing 1 of the following medically acceptable methods of birth control and agrees to continue with the regimen throughout the duration of the study:
• Oral, implantable or injectable contraceptives for 3 consecutive months before the baseline/randomization visit
• Total abstinence from sexual intercourse (>= 1 complete menstrual cycle before the baseline/randomization visit)
• Intrauterine device (IUD)
• Double barrier method (condoms, sponge, diaphragm or vaginal ring with spermicidal jellies or cream)
• PART II:
• To be eligible for inclusion in Part II, patients must meet the eligibility for Part 1 as well as the following:
• Patients with histologically confirmed HCC for whom there is no standard/approved chemotherapy

Exclusion Criteria:

• New York Heart Association Class III or IV, cardiac disease, myocardial infarction within the past 6 months, unstable arrhythmia, or evidence of ischemia on electrocardiogram (ECG)
• Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy
• Pregnant or nursing women; NOTE: Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately
• Treatment with radiation therapy, surgery, chemotherapy, or investigational therapy within one month prior to study entry
• Unwillingness or inability to comply with procedures required in this protocol
• Known infection with human immunodeficiency virus (HIV)
• Serious nonmalignant disease (e.g., hydronephrosis, liver failure, or other conditions) that could compromise protocol objectives in the opinion of the Investigator and/or the Sponsor
• Patients who are currently receiving any other investigational agent
• Patients who are receiving drugs that are sensitive substrates of CYP450 1A2, 3A4, 2C9, 2C19 or 2D6, or strong inhibitors or inducers of all major CYP450 isozymes that cannot be stopped at least 7 days or 5 half-lives (whichever is longer) before starting treatment with ABC294640 and either replaced with another appropriate medication or not given for the duration of the clinical study
• Patients who are currently taking Coumadin or Coumadin derivatives
• Patients who have received any antineoplastic therapy within 1 month of starting treatment with ABC294640 or who have not adequately recovered from side effects and toxicities of previous antineoplastic therapy

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: NA
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Treatment (enzyme inhibitor therapy); Patients receive sphingosine kinase-2 inhibitor ABC294640 PO BID on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.	Drug: sphingosine kinase-2 inhibitor ABC294640; Given PO Starting dose of ABC294640 250 mg once on day on Days 1-28 of each 28-day cycle. Subsequent cohort doses (if reached) are as follows: 250 BID, 500 BID, 750 BID, 1,000 BID, 1,500 BID, 2,000 BID, 2,500 BID; Other Names: SK2 inhibitor ABC294640

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Maximum tolerated dose (MTD) defined as highest dose of ABC294640 at which 0 or 1 patient of 6 experiences a DLT.	MTD defined as the highest dose at which 0 or 1 patient of 6 experiences a DLT. The DLT rate will be estimated with its 95% confidence interval.	Patients will be followed until the point in time when no more than 1 of 6 patients has a Dose Limiting Toxicity (DLT) in cycle 1, and expected 54 days.
Safety assessed using the National Cancer Institute (NCI) Common Toxicity Criteria (CTC) version 4.0.	Assessed using the National Cancer Institute (NCI) Common Toxicity Criteria (CTC) version 4.0. Adverse events (AEs) will be coded by body system and summary tables with incidence rates of adverse events will be generated. Descriptive statistics of AEs will be reported by doses and for subsets of patients with serious adverse events (SAEs), patients who discontinue due to AEs, and patients with related AEs.	Weekly during course 1, bi-weekly for all subsequent courses, and at the end of treatment study-- expected to occur at an average of 6 months from study start.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pharmacodynamic parameters for sphingosine kinase-2 inhibitor ABC294640	Area under the drug concentration over time curve (AUC), maximum concentration, minimum concentration, and time to maximum concentration will be calculated for each subject.	Days 1 and 28 of cycle 1 collected at prior to dose, 1, 2, 4, 8, 12, 24 hours post drug administration.
Pharmacodynamic parameters for sphingosine kinase-2 inhibitor ABC294640	Pharmacodynamic parameters for ABC294640 action will include measurement of plasma levels of S1P, including absolute concentration at each sampling time and chance from baseline concentration at each sampling time after drug administration.	Weekly during course 1, bi-weekly for all subsequent courses, and at the end of treatment study-- expected to occur at an average of 6 months from study start.
Tumor response rate	All patients who have measureable disease according to RECIST 1.1, received at least one cycle of treatment, and have had disease re-evaluated will be included.	Every 8 weeks till end of treatment study-- expected to occur at an average of 6 months from study start.

Collaborators and Investigators

• Sponsor: RedHill Biopharma Limited
• Collaborators: Medical University of South Carolina; National Cancer Institute (NCI); FDA Office of Orphan Products Development; Apogee Biotechnology Corporation
• Investigators: Principal Investigator: Carolyn Britten, MD, Medical University of South Carolina

Study record dates

Study Major Dates

• Study Start: August 1, 2011
• Primary Completion (ACTUAL): August 1, 2014
• Study Completion (ACTUAL): July 1, 2015

Study Registration Dates

• First Submitted: September 29, 2011
• First Submitted That Met QC Criteria: December 7, 2011
• First Posted (ESTIMATE): December 8, 2011

Study Record Updates

• Last Update Posted (ACTUAL): January 7, 2020
• Last Update Submitted That Met QC Criteria: January 4, 2020
• Last Verified: August 1, 2015

More Information

Terms related to this study

• Keywords: ABC294640; RedHill Biopharma, Ltd.; ABC-101; Medical University of South Carolina; Apogee Biotechnology Corporation
• Other Study ID Numbers: CTO 101504; NCI -2011-02993 (REGISTRY: CTRP(Clinical Trial Reporting Program)); G04102-00 (OTHER_GRANT: OOPD); R01FD004102-01 (FDA)