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Phase I, Multi-Center, Open-Label, Dose Escalation Study of HuLuc63 (Humanized Anti-CS1 Monoclonal IgG1 Antibody) in Subjects With Advanced Multiple Myeloma


Phase 1
18 Years
N/A
Not Enrolling
Both
Multiple Myeloma

Thank you

Trial Information

Phase I, Multi-Center, Open-Label, Dose Escalation Study of HuLuc63 (Humanized Anti-CS1 Monoclonal IgG1 Antibody) in Subjects With Advanced Multiple Myeloma


Inclusion Criteria:



Eligible subjects will be considered for inclusion in this study if they meet all of the
following criteria:

- Males or females, age 18 years or older.

- Diagnosis of advanced multiple myeloma, after at least 2 prior therapies for MM.

- Measurable disease M component in serum (at least 0.5 G/dL) and/or urine (≥0.2 g
excreted in a 24-hour collection sample).

- Not eligible for stem cell or bone marrow transplant or have refused stem cell or
bone marrow transplant or have relapsed after autologous or allogeneic stem cell or
bone marrow transplant.

- ECOG performance status 0-2 (Appendix E).

- ALT or AST ≤3 x ULN.

- Total bilirubin ≤2 x ULN (unless related to MM).

- Serum creatinine ≤2.0 mg/dL (unless related to MM, then ≤ 3.0 mg/dL).

- Must have adequate bone marrow function defined as: Absolute neutrophil count >1,000
cells/mm3; platelets ≥75,000 cells/mm3; and hemoglobin ≥8 g/dL. No platelet
transfusion within 72 hours of obtaining screening platelet count.

- Serum calcium (corrected for albumin) level within normal range (treatment of
hypercalcemia is allowed and subject may enroll if hypercalcemia returns to normal
with treatment).

- Signed and dated informed consent.

- Use of appropriate contraception where applicable.

- Negative pregnancy test within 48 hours prior to first dose in women of childbearing
potential.

- Must have 2-dimensional echocardiogram or MUGA indicating LVEF ≥ 45% within 30 days
prior to first dose of study drug.

- Ability to understand the purpose and risks of the study and provide signed and dated
informed consent and authorization to use protected health information (in accordance
with national and local subject privacy regulations).

Exclusion Criteria:

Subjects will be ineligible for this study if they meet any one of the following criteria:

- Life expectancy of less than 3 months.

- Prior malignancy, except for adequately treated basal cell or squamous cell skin
cancer, in situ cervical cancer, or other cancer from which the subject has been
disease-free for at least 5 years.

- Plasma cell leukemia (active or prior).

- Uncontrolled medical problems such as diabetes mellitus, coronary artery disease,
hypertension, unstable angina, arrhythmias, pulmonary, hepatic, and renal diseases
unless renal insufficiency is felt to be secondary to multiple myeloma (serum
creatinine > 2.0 mg/dL).

- Solitary bone or solitary extramedullary plasmacytoma as the only evidence of plasma
cell dyscrasia.

- Corticosteroid, Velcade® or other proteosome inhibitor, thalidomide, lenalidomide
(Revlimid®), or melphalan within 2 weeks of the first dose of HuLuc63; nitrogen
mustard agents within 6 weeks of the first dose of HuLuc63.

- Investigational drug within 4 weeks or 5 half-lives (whichever is greater) of the
first dose of HuLuc63.

- Stem cell or bone marrow transplant within 12 weeks prior to the first dose of
HuLuc63.

- Biological agents including intravenous immune globulin (IVIG) and monoclonal
antibodies within 4 weeks of the first dose of HuLuc63.

- Neuropathy >Grade 2 (according to the NCI CTCAE v3.0 criteria scale).

- Symptomatic orthostatic hypotension.

- Evidence of amyloidosis.

- Known active infections requiring antibiotics, antivirals, or antifungals.

- Serious psychiatric illness, active alcoholism, or drug addiction that may hinder or
confuse follow-up evaluation.

- Hypersensitivity to recombinant proteins or excipients in the investigational agent.

- Any condition that in the investigator's opinion makes the subject unsuitable for
study participation.

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Not applicable for this trial.

Outcome Time Frame:

Not applicable for this trial.

Safety Issue:

No

Principal Investigator

William Bensinger, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Fred Hutchinson Cancer Research Center

Authority:

United States: Food and Drug Administration

Study ID:

HuLuc63-1701

NCT ID:

NCT00425347

Start Date:

December 2006

Completion Date:

July 2009

Related Keywords:

  • Multiple Myeloma
  • Multiple myeloma, MM, plasma cell myeloma, cancer
  • Multiple Myeloma
  • Neoplasms, Plasma Cell

Name

Location

Fred Hutchinson Cancer Research CenterSeattle, Washington  98109
Dana-Farber Cancer InstituteBoston, Massachusetts  02115
Arkansas Cancer Research CenterLittle Rock, Arkansas  72205
Cleveland ClinicCleveland, Ohio  44195
Wayne State UniversityDetroit, Michigan  48202
Northwestern University Feinberg School of MedicineChicago, Illinois  60611
USC/Norris Cancer HospitalLos Angeles, California  90033
University of Massachusetts Memorial Healthcare- Univ. CampusWorcester, Massachusetts  01655