Safety and Pharmacokinetics of Rising Doses of APO010 in Relapsed/Refractory Multiple Myeloma Patients Selected by DRP

NCT ID: NCT03196947

Last Updated: 2020-01-30

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-06-13
• Study Completion Date: 2020-01-16

Brief Summary

Multicentre, open label, uncontrolled, phase I pharmacokinetic study, to determine the Maximum Tolerated Dose (MTD) of APO010 administered intravenously on D1, D8 and D15 followed by a one-week drug rest, in patients with multiple myeloma for who have relapsed or are refractory to 2 (in high-risk patients 1) or more different prior therapies and who have Drug Response Predictor (DRP) for APO010 indicating a higher likelihood for response to APO010. The study will contain an extension phase where the recommended Dose will be tested on additional patients.

Detailed Description

APO010 is a novel investigational antitumour agent. It is a recombinant form of human Fas ligand (FasL), a protein with the function of inducing programmed cell death (apoptosis). Preclinical studies indicate that multiple myeloma is sensitive for APO010. Estimation of DRP for APO010 in myeloma patients suggests that it may be possible to identify patients with high and low likelihood for response, and thereby allocate the predicted high likelihood patients to the treatment. Preclinical results indicate that, in comparison with other single agents, APO010 exercises superior anti-tumour effect by inducing apoptosis.

The study will include patients with multiple myeloma who have relapsed or are refractory to 2 (in high-risk patients 1) or more different prior therapies, including IMiDs and PI and who have Drug Response Predictor (DRP) for APO010 indicating a higher likelihood for response to APO010.

This study is a multicentre, open label, uncontrolled, phase I, dose escalation, pharmacokinetic study, to determine the Maximum Tolerated Dose (MTD) of APO010 administered intravenously on D1, D8 and D15 followed by a one-week drug rest i.e. cycle duration is 4 weeks. The study will contain an extension phase where the Recommended Dose will be tested on additional patients.

The primary endpoint is determination of the Maximum Tolerated Dose (MTD)based upon first cycle drug-related dose-limiting toxicity and the recommended dose of APO010. Safety will be evaluated during the study and for 30 days after the last administration of study drug. Adverse events and laboratory studies will be graded according to NCI-CTCAE v. 4.03.

The proportion of patients with positive HADA assessment will be investigated and a description of any objective tumour response based on International Myeloma Working Group criteria and from changes in M-protein and iFLC.

Conditions

Relapsed/Refractory Multiple Myeloma

Study Design

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

Study Groups

Single arm, APO010 Dose escalation

Group Type: EXPERIMENTAL

APO010

Intervention Type: DRUG

APO010 is given iv on D1, D8 and D15 followed by a one-week drug rest (cycle duration 4 weeks).

Interventions

APO010

APO010 is given iv on D1, D8 and D15 followed by a one-week drug rest (cycle duration 4 weeks).

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Relapsed or relapsed/refractory to 2 (in high-risk patients 1) or more different prior therapies, including IMiDs and PI
• Measurable disease
• Serum M-protein > 10 g/l, or
• Urine M-protein > 200 mg/24 hours, or
• Serum involved-FLC (iFLC) > 100 mg/l and abnormal FLC ratio
• Have participated in the APO010 screening protocol in which Drug Response Predictor (DRP) outcome is measured as being in the upper likelihood of response (50% in dose-finding part and 25% in the expansion cohort)
• Age > 18 years
• Adequate organ and bone marrow function as defined below:
• Absolute neutrophil count > 1.5 x 109/l (> 0.75 x 109/l in case > 50% plasma cell count in bone marrow)
• Platelet count > 50 x 109/l (> 30 x 109/l in case > 50% plasma cell count in bone marrow)
• Haemoglobin > 4.6 mmol/l (> 7.5 g/l)
• Bilirubin ≤ upper limit of normal
• aspartate aminotransferase (SGOT)/alanine transaminase (SGPT) ≤ upper limit of normal
• Creatinine < 1.5 x upper limit of normal or creatinine clearance > 50 ml/min calculated according to Cockcroft-Gault
• Eastern Cooperative Oncology Group (ECOG) performance status < 2
• Life expectancy of at least 3 months.
• Capability of understanding the nature of the study and giving written informed consent
• Signed informed consent form

Exclusion Criteria

• Have central nervous system (CNS) myeloma
• Have plasma cell leukaemia defined as plasma cell count > 2000 / µL in peripheral blood
• Have symptomatic amyloidosis
• Have anti-myeloma treatment or radiotherapy within 3 weeks from first infusion
• Have received a cumulative dose of corticosteroid > 200 mg (dexamethasone, or equivalent dose of prednisone) within 2 weeks of the first infusion
• Have received any experimental drug or experimental therapy within 3 weeks before the first infusion
• Have received autologous-stem cell transplantation (SCT) within 12 weeks before the first infusion
• Have received an allogeneic stem cell transplantation (SCT)
• Have had past or current malignancy except for:
• Cervical carcinoma < Stage 1B
• Non-invasive basal cell or squamous cell skin carcinoma
• Malignant melanoma with CR of > 10 years
• Any other curable cancer with a CR > 5 years
• Have major surgery within 4 weeks prior to the first infusion
• Have severe infection requiring iv treatment
• Have known HIV positivity
• Have known active hepatitis B or C
• Have had clinical significant arteriosclerotic events:
• Ischemic heart disease
• Unstable angina
• Myocardial infarction
• Transient ischemic attack
• Ischemic stroke
• Documented peripheral arteriosclerosis
• Have baseline QT interval as corrected by Fridericia's formula (QTcF) > 470 msec for female patients or > 450 msec for male patients or a complete left bundle branch block (defined as QRS interval > 120 msec in left bundle branch block form)
• CNS disease including epilepsy or altered mental status precluding understanding of the informed consent process and/or completion of the necessary study procedures
• Women of childbearing age and potential who are not willing to use effective contraception during the study and at least until 90 days after last dose of study drug. Male patients or male patients who have female partners of childbearing age and potential who are not willing to use effective contraception during the study and at least until 90 days after last dose of study drug. Highly effective methods of birth control are defined as those which result in a low failure rate, i.e., less than 1% per year, when used consistently and correctly such as implants, injectables, combined oral contraceptives, some intra-uterine devices, sexual abstinence or vasectomized partner
• Pregnant or breast-feeding women

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

Sponsors

Smerud Medical Research International AS

OTHER

Sponsor Role: collaborator

Medical Prognosis Institute A/S

INDUSTRY

Sponsor Role: collaborator

Allarity Therapeutics

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Annette J Vangsted, DMSc

Role: PRINCIPAL_INVESTIGATOR

Rigshospitalet, Finsen Centre, Hematological Department,, Phase 1 Unit

Locations

University Hospital of Copenhagen

Copenhagen, , Denmark

Countries

Denmark

Other Identifiers

APO010/P1/002

Identifier Type: -

Identifier Source: org_study_id