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A Safety Study of SGN-CD48A in Patients With Multiple Myeloma

Phase 1
Terminated
Conditions
Multiple Myeloma
Interventions
Registration Number
NCT03379584
Lead Sponsor
Seagen Inc.
Brief Summary

This study will test the safety and activity of SGN-CD48A in patients with multiple myeloma. SGN-CD48A will be given on Days 1, 8, and 15 of a 28-day cycle. Prior to protocol amendment 2, SGN-CD48A was given every 3 weeks.

Detailed Description

This study is designed to evaluate the safety, tolerability, and antitumor activity of SGN-CD48A in patients with relapsed or refractory multiple myeloma. This study will be conducted in 2 parts:

1. Dose escalation: This part will evaluate increasing doses of SGN-CD48A to identify the maximum tolerated dose.

The first group of patients enrolled on the study will receive the lowest dose of SGN-CD48A. Once this dose is shown to be safe, a second group of patients will be enrolled at the next higher dose. Patients will continue to be enrolled in groups receiving increasing doses until the maximum tolerated dose level is reached. Patients can only be enrolled into a higher dose level once the lower doses have been demonstrated safe. Dose escalation will be conducted using a modified toxicity probability interval (mTPI) study design.

2. Dose expansion: This part will further evaluate the safety, tolerability, and antitumor activity of up to 2 dose levels of SGN-CD48A shown to be safe in the first part of the trial.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
14
Inclusion Criteria
  • Diagnosis of MM requiring systemic therapy (per the International Myeloma Working Group [IMWG])
  • Patients must not have other therapeutic options known to provide clinical benefit in MM available to them. Prior lines of therapy must include at least a proteasome inhibitor, an immunomodulatory drug, and an anti-CD38 antibody.
  • Measureable disease, as defined by at least one of the following: serum M protein 0.5 g/dL or higher, urine M protein 200 mg/24 hour or higher, and serum immunoglobulin free light chain 10 mg/dL or higher and abnormal serum immunoglobulin kappa lambda free light chain ratio
  • Adequate hematologic, renal, and hepatic function
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Life expectancy greater than 3 months
  • A negative pregnancy test (for females of childbearing potential)
  • Patients must provide written consent
Exclusion Criteria
  • Pre-existing peripheral neuropathy Grade 2 or higher
  • History of malignancy other than MM within the past 3 years
  • Active cerebral/meningeal disease related to the underlying malignancy
  • Uncontrolled Grade 3 or higher infection
  • Known to be positive for HIV or hepatitis B, or known to have active hepatitis C infection
  • Previous allogeneic stem cell transplant
  • History of cerebral vascular event, unstable angina, myocardial infarction, or cardiac symptoms consistent with congestive heart failure within the last 6 months
  • Treatment with any known P-gp inducers/inhibitors or strong CYP3A inhibitors within 14 days prior to the first dose of study drug
  • Prior antitumor therapy that is not completed at least 4 weeks prior to first dose of study drug, or at least 2 weeks if progressing. Prior CAR T-cell therapy must be completed 8 weeks before first dose of study drug.
  • Females who are pregnant or breastfeeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
SGN-CD48ASGN-CD48ASGN-CD48A
Primary Outcome Measures
NameTimeMethod
Incidence of laboratory abnormalitiesThrough 1 month following last dose
Type, incidence, severity, seriousness, and relatedness of adverse eventsThrough 1 month following last dose
Incidence of dose limiting toxicityThrough 3 weeks following first dose
Secondary Outcome Measures
NameTimeMethod
Objective response rateThrough 1 month following last dose

The proportion of patients with stringent complete response, complete response, very good partial response, or partial response per investigator

Complete response rateThrough 1 month following last dose

The proportion of patients with stringent complete response or complete response per investigator

Duration of objective responseUp to approximately 3 years
Duration of complete responseUp to approximately 3 years
Progression-free survivalUp to approximately 3 years
Overall survivalUp to approximately 3 years
Blood concentrations of SGN-CD48A and metabolitesThrough 1 month following last dose
Incidence of antitherapeutic antibodiesThrough 1 month following last dose

Trial Locations

Locations (6)

Yale Cancer Center

🇺🇸

New Haven, Connecticut, United States

University of California at San Francisco

🇺🇸

San Francisco, California, United States

H. Lee Moffitt Cancer Center and Research Institute

🇺🇸

Tampa, Florida, United States

Levine Cancer Institute

🇺🇸

Charlotte, North Carolina, United States

Mount Sinai Medical Center

🇺🇸

New York, New York, United States

University of Pennsylvania / Perelman Center for Advanced Medicine

🇺🇸

Philadelphia, Pennsylvania, United States

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