A Phase I, Multi-Dose Study of SGN-40 (Anti-huCD40 mAb) in Patients With Refractory or Recurrent Multiple Myeloma
SGN-40 (anti-huCD40 mAb)
Blood Protein Disorders+11
+ Cardiovascular Diseases
+ Hematologic Diseases
Treatment Study
Summary
Study start date: March 1, 2004
Actual date on which the first participant was enrolled.This is an open-label, multi-dose, single-arm, phase I, dose-escalation study to define the toxicity profile, maximum tolerated dose (MTD), pharmacokinetics, and antitumor activity of SGN-40 in patients with refractory or recurrent multiple myeloma. A minimum of three patients will be entered into each dose-level cohort. All patients will receive a dose-loading schedule during the first two weeks. The maximum weekly dose will be 16mg/kg.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.44 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: 1. Patients must have refractory or recurrent secretory multiple myeloma (MM). 2. Patients must have failed at least two different prior systemic therapies for MM. 3. Patients may have received a maximum of five cytotoxic regimens. 4. Patients who have received any of the following must complete within the specified time frame below: * Autologous stem cell transplant - 12 weeks prior to first dose * Nitrogen Mustard agents, Melphalan, BCNU, IVIG, or monoclonal antibody therapy - 6 weeks prior to first dose * Chemotherapy, Radiation, or other therapies for MM - 4 weeks prior to first dose 5. Patients who have not undergone autologous stem cell transplantation must be either ineligible for stem cell transplantation or, if eligible, must have refused treatment by autologous stem cell transplantation. 6. Patients must have an ECOG performance status of ≤ 2 and a life expectancy \> three months. 7. Patients must be available for periodic blood sampling, study-related assessments, and management of toxicity at the treating institution for the entire duration of the study. 8. Patients must be at least 18 years of age. 9. Females of childbearing potential must have a negative β-HCG pregnancy test result within three days of enrollment. All patients must plan to use an effective contraceptive method during the course of the study. 10. Patients must meet baseline lab data requirements. 11. Patients must give written informed consent. Exclusion Criteria: 1. Patients with non-secretory MM or solitary plasmacytoma or plasma cell leukemia. 2. Patients with a history of allogeneic transplantation. 3. Patients receiving plasmapheresis within four weeks prior to enrollment. 4. Patients undergoing major surgery within four weeks prior to enrollment. 5. Patients with a known hypersensitivity to recombinant proteins or any excipient contained in the drug formulation. 6. Patients with a history of other malignancies during the past five years with the exception of adequately treated basal or squamous cell skin cancer or cervical carcinoma in situ. 7. Patients with any active viral, bacterial, or systemic fungal infection within four weeks of enrollment. 8. Patients with a history of significant chronic or recurrent infections requiring treatment. 9. Patients with a history of active thrombosis within three months of enrollment. 10. Patients with a history of pulmonary embolism. 11. Patients with a history of migraines or severe headaches requiring medical therapy within 12 months of enrollment. 12. Patients who are pregnant or breastfeeding. 13. Patients with uncontrolled hypercalcemia. 14. Patients with any serious underlying medical condition that would impair their ability to receive or tolerate the planned treatment. 15. Patients with dementia or altered mental status that would preclude understanding and rendering of informed consent.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 5 locations
Rocky Mountain Cancer Center
Denver, United StatesDana Farber Cancer Institute
Boston, United StatesCornell University
New York, United States