L-DOS47 Plus Doxorubicin in Advanced Pancreatic Cancer

NCT ID: NCT04203641

Last Updated: 2025-05-06

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 28 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-12-11
• Study Completion Date: 2024-10-24

Brief Summary

This study will evaluate the safety and tolerability of escalating doses of L-DOS47 in combination with doxorubicin, as well as preliminary anti-tumor activity in patients with previously treated advanced pancreatic cancer.

Detailed Description

The Phase Ib part of the study will apply a standard 3 + 3 algorithm for dose escalation to determine the appropriate L-DOS47 maximum tolerated dose to use in combination with doxorubicin for the Phase II part of the study. Patients will be recruited into 3 cohorts where each cohort will receive increasing weekly dose levels of L-DOS47 in combination with a fixed dose of 20 mg/m2 of doxorubicin weekly. The decision for escalation to the next dose level will be made after all patients in a cohort have completed 4 weeks of combination treatment and the safety data have been reviewed by the Safety Review Committee. If a patient in any cohort experiences a dose limiting toxicity, an additional 3 patients will be enrolled, for a maximum of up to 18 patients in this initial dose escalation part of the study.

The Phase II part of the study will focus on evaluating preliminary anti-tumor activity, as well as continuing to evaluate safety and tolerability of L-DOS47 in combination with doxorubicin. A further 11 additional patients will be enrolled in this phase of the study, which is designed to ensure patient safety and to detect whether there is a level of anti-tumor activity that would be worth pursuing in a larger clinical trial. Patients will be initiated on the L-DOS47 dose determined in Phase I, in combination with 20 mg/m2 doxorubicin, with tumor marker carbohydrate antigen 19-9 (CA19-9) measurements at each treatment cycle, and radiological assessments every two treatment cycles.

Tumor response will be assessed according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 criteria.

Safety will be assessed by reported adverse events (AEs), serious adverse events (SAEs), physical exams, vital signs, Karnofsky Performance Status, electrocardiogram (ECG), echocardiogram (ECHO)/multigated acquisition scan (MUGA), clinical laboratory evaluations (hematology, chemistry, coagulation and urinalysis), and anti-L-DOS47 antibody levels.

Conditions

Pancreas Cancer

Study Design

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

Study Groups

L-DOS47 + doxorubicin

Patients will be recruited into escalating dosing cohorts of 3, 6 and 9 µg/kg of L-DOS47, with a minimum of 3 and a maximum of 6 patients per cohort. A fixed dose of intravenous doxorubicin \[20 mg/m2/week\] will be administered in combination with L-DOS47 across all cohorts.

Group Type: EXPERIMENTAL

L-DOS47

Intervention Type: BIOLOGICAL

A treatment cycle will be 28 days, with patients receiving L-DOS47 on Days 1, 8, 15, and 22.

Doxorubicin

Intervention Type: DRUG

A treatment cycle will be 28 days, with patients receiving doxorubicin on Days 2, 9, 16 and 23

Interventions

L-DOS47

A treatment cycle will be 28 days, with patients receiving L-DOS47 on Days 1, 8, 15, and 22.

Intervention Type: BIOLOGICAL

Doxorubicin

A treatment cycle will be 28 days, with patients receiving doxorubicin on Days 2, 9, 16 and 23

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male or female aged ≥ 18 years old

2. One or more metastatic tumors measurable on computed tomography (CT) scan per RECIST version 1.1 and screening FDG-PET scan with maximum standardized uptake value (SUV max) ≥ 5.5 for at least one lesion consistent with pancreatic cancer.

3. Karnofsky performance status ≥ 70%

4. Life expectancy of at least 3 months

5. Able to understand the information provided to them and to give written institutional review board (IRB)-approved informed consent prior to any study activities being conducted

6. A negative pregnancy test (if of child bearing potential)

7. Acceptable liver function:

1. Bilirubin ≤ 1.5 times upper limit of normal

2. Aspartate aminotransferase (AST), alanine aminotransferase (ALT) and Alkaline phosphatase (ALP) ≤ 2.5 times upper limit of normal (ULN; if liver metastases are present, then ≤ 5 x ULN is allowed)

8. Acceptable renal function as defined by creatinine ≤1.5x institutional upper limits of normal, or calculated creatinine clearance ≥ 60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal

9. Acceptable hematologic status:

1. Granulocyte ≥ 1500 cells/mm3

2. Platelet count ≥ 100,000 (plt/mm3)

3. Hemoglobin ≥ 9g/dL

10. Urinalysis:

a) No clinically significant abnormalities

11. Acceptable coagulation status

1. Prothrombin time within 1.5x of normal limits

2. Partial thromboplastin time (PTT) within 1.5x of normal limits

12. For men and women of child-bearing potential, the use of effective contraceptive methods during the study

13. Normal ejection fraction on ECHO or MUGA

Exclusion Criteria

1. New York Heart Association Class III or IV, cardiac disease, myocardial infarction within the past 6 months, unstable arrhythmia, or evidence of ischemia on ECG

2. Abnormal ejection fraction on ECHO or MUGA

3. Active, uncontrolled bacterial, viral, or fungal infections requiring systematic therapy

4. Pregnant or nursing women. NOTE: Women of childbearing 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 while participating in this study, she should inform her treating physician immediately.

5. Treatment with radiation therapy, surgery, chemotherapy, or investigational therapy within 3 weeks prior to study entry

6. Major surgery within 4 weeks prior to study entry

7. Unwillingness or inability to comply with procedures required in this protocol

8. Known infection with HIV, hepatitis B, or hepatitis C

9. Serious nonmalignant disease (eg hydro nephrosis, liver failure, or other conditions) that could compromise protocol objectives in the opinion of the investigator and/or the sponsor

10. Patients who are currently receiving any other investigational agent

11. Patients with any evidence of uncontrolled brain metastases or carcinomatosis meningitis.

12. Patients with marked screening prolongation of QT/QTc interval (e.g. repeated demonstration of a QTc interval > 480 milliseconds (CTCAE grade 1) using Fredericia's QT correction formula.

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

Sponsors

Theradex

INDUSTRY

Sponsor Role: collaborator

Helix BioPharma Corporation

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Erkut Borazanci, MD

Role: PRINCIPAL_INVESTIGATOR

Scottsdale Healthcare Hospitals DBA HonorHealth

Locations

Scottsdale Healthcare Hospitals DBA HonorHealth

Scottsdale, Arizona, United States

Atlantic Health System, Morristown Medical Center

Morristown, New Jersey, United States

Froedtert Hospital and the Medical College of Wisconsin

Milwaukee, Wisconsin, United States

Countries

United States

Other Identifiers

LDOS006

Identifier Type: -

Identifier Source: org_study_id