Dose Escalation Study of I-131-CLR1404 in Patients With Relapsed or Refractory Multiple Myeloma
Conditions
Multiple Myeloma
Conditions: official terms
Multiple Myeloma - Neoplasms, Plasma Cell
Conditions: Keywords
Multiple Myeloma, Radiopharmaceutical, Therapy, Phase 1
Study Type
Interventional
Study Phase
Phase 1
Study Design
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Intervention
Name: I-131-CLR1404 Type: Drug
Name: dexamethasone Type: Drug
Overall Status
Recruiting
Summary
The primary objective of the study is to determine the safety and tolerability of I-131-CLR1404, with and without concurrent weekly dexamethasone, in patients with relapsed or refractory multiple myeloma who have previously been treated with, or are intolerant of, an immunomodulator and a proteasome inhibitor.
Detailed Description
Multiple myeloma (MM) is an incurable, monoclonal proliferation of plasma cells. Approximately 80,000 Americans are affected by MM with approximately 22,000 new cases diagnosed and 11,000 deaths each year. The introduction of newer therapies in the past twenty years, such as autologous stem cell transplantation and novel agents such as proteasome inhibitors and immune modulating drugs has improved outcomes, with current median overall survival estimates of 3-10 years depending on a number of patient-, disease- and treatment-related factors. However, despite these innovations, myeloma relapse is inevitable. Therefore, there is a clear need for improved therapies for MM and, in particular, for relapsed disease.

I-131-CLR1404 is a radioiodinated therapeutic that exploits the selective uptake and retention of phospholipid ethers (PLEs) by malignant cells. Cellectar Biosciences' novel cancer-targeted small-molecule compound (CLR1404) is radiolabeled with the isotope iodine-131 (I-131). Radioiodinated CLR1404 has been evaluated in over 60 xenograft and spontaneous (transgenic) tumor models. In all but two cases of hepatocellular carcinoma, CLR1404 demonstrated selective cancer cell uptake and retention. In various rodent tumor models, I-131-CLR1404 has also demonstrated tumor growth delay and prolongation of survival.

Based on the critical unmet medical need for effective agents with novel mechanisms of action in MM, the exquisite radiosensitivity of MM, and initial preclinical and clinical experience with radioiodinated CLR1404, Cellectar Biosciences has chosen to assess I-131-CLR1404 in a MM-specific phase 1 trial.
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: N/A
Minimum Age: 18 Years
Gender: Both
Criteria: Inclusion Criteria:

- Histologically or cytologically confirmed multiple myeloma

- Prior treatment with or intolerance to proteasome inhibitor and immunomodulator

- Bone marrow biopsy within 28 days of study drug infusion demonstrating at least 5% plasma cell involvement

- Progressive disease defined by any of following:

25% increase in serum M-protein from lowest response value during (or after) last therapy and/or absolute increase in serum M-protein of > 0.5 g/dL; 25% increase in urine M-protein from lowest response value during (or after) last therapy and/or absolute increase in urine M-protein of > 200 mg/24h; 25% increase in bone marrow plasma cell percentage from lowest response value during (or after) last therapy - absolute bone marrow plasma cell percentage must be > 10% unless prior complete response when absolute bone marrow plasma cell percentage must be > 5%; new onset hypercalcemia > 11.5 mg/dL

- Measurable disease defined by any of following: Serum M-protein > 1 g/dL; Urine M-protein > 200 mg/24h; Serum free light chain (FLC) assay: involved FLC level > 10 mg/dL provided serum FLC ratio is abnormal

- Eastern Cooperative Oncology Group performance status of 0 to 2

- Life expectancy of at least 6 months

- Have initiative and means to be compliant with protocol and within geographical proximity to make required study visits as judged by Investigator

- Subject or legal representative has ability to read, understand and provide written informed consent for study related procedures

- Women of childbearing potential must have negative pregnancy test within 24 hours of enrollment

- Women of childbearing potential and men who are able to father a child, must agree to use an effective contraception method during study and for 12 months following study drug administration

Exclusion Criteria:

- Grade 2 or greater toxicities due to previous therapies, subject to laboratory abnormalities listed below. Stable, tolerable Grade 2 adverse events may be allowed at discretion of Investigator

- Prior external beam radiation therapy resulting in greater than 20% total bone marrow receiving greater than 20 Gy

- Prior radioisotope therapy

- Prior total body or hemi-body irradiation

- More than one previous, alkylator-based chemotherapy regimen. Transplantation is considered one alkylator-based chemotherapy regimen. Immunomodulators and proteasome inhibitors are not considered alkylator-based chemotherapy regimens

- Subject has received severely marrow toxic drugs

- Extradural tumor in contact with the spinal cord or tumor located where swelling in response to therapy may impinge upon spinal cord

- Subject has any of following laboratory abnormalities: Platelets < 125,000/L; WBC < 3000/L; ANC < 1500/L; Hemoglobin < 8 g/dL; Estimated glomerular filtration rate < 30 mL/min/1.73 m2; ALT > 3 x ULN ; Bilirubin > 1.5 x ULN

- Chronic immunosuppressive and/or full-dose anticoagulant therapy

- Anti-platelet therapy, except low-dose aspirin for cardioprotection

- PTT > ULN

- INR > ULN

- Radiation therapy, chemotherapy, immunotherapy, investigational therapy or corticosteroid use within 4 weeks of or after eligibility-defining bone marrow biopsy. Bisphosphonates and denosumab are permitted if subject has been receiving for at least 90 days

- History of hypersensitivity to iodine

- Any other concomitant serious illness or organ system dysfunction in opinion of Investigator would either compromise subject safety or interfere with test drug safety evaluation

- Major surgery within 6 weeks of enrollment

- Known history of HIV, hepatitis C or hepatitis B infection

- Pregnancy or breast-feeding
Locations
Mayo Clinic
Jacksonville, Florida, United States
Status: Recruiting
Contact: Michele Maharaj - 904-953-6136 - maharaj.michele@mayo.edu
University of Wisconsin Hospital and Clinics
Madison, Wisconsin, United States
Status: Recruiting
Contact: UW Cancer Connect - 800-622-8922
Start Date
February 2015
Completion Date
December 2016
Sponsors
Cellectar Biosciences, Inc.
Source
Cellectar Biosciences, Inc.
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page