Study of ACTR087 in Combination With SEA-BCMA in Subjects With Relapsed or Refractory Multiple Myeloma

Overview

About this study

This is a phase 1, multi-center, single-arm, open-label study evaluating the safety, tolerability, and anti-myeloma activity of ACTR087 (an autologous T cell product) in combination with SEA-BCMA (a monoclonal antibody) in subjects with relapsed or refractory Multiple Myeloma.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria: 

  • Signed written informed consent obtained prior to study procedures.
  • Histologically- or cytologically-confirmed relapsed or refractory multiple myeloma (MM) with measurable disease .
  • Must have received at least 3 prior lines of therapy to include treatment with a proteasome inhibitor (eg, bortezomib, carfilzomib, or ixazomib) and an immunomodulatory agent (eg, lenalidomide, pomalidomide) unless double-refractory to both; and a hematopoietic stem cell transplant (HSCT), for those subjects considered HSCT-eligible. 
  • Quantitative serum IgG levels for subjects with IgG MM must not exceed the institutional upper limit of normal (ULN).
  • ECOG 0 or 1 - Life expectancy of at least 6 months.
  • Absolute neutrophil (ANC) count greater than 1000/ µL.
  • Platelet count greater than 50,000/µL. 
  • Estimated GFR >30mL/min/1.73m2.

Exclusion Criteria: 

  • Known active central nervous system (CNS) involvement by MM.
  • Systemic rheumatic or autoimmune diseases or acute or chronic infections .
  • Uncontrolled thromboembolic events or recent severe hemorrhage.
  • Subjects who are currently using more than 5mg/day of prednisone (or an equivalent glucocorticoid exceeding physiologic replacement levels). 
  • Prior treatment as follows:
    • T cell-directed antibody therapy (eg. Alemtuzumab, anti-thymocyte globulin) within 6 months of enrollment;
    • Any prior myeloma-directed therapy including cytotoxic chemotherapy, biologic therapy, or radiotherapy within 2 weeks of enrollment; 
    • Any mAb or other protein therapeutic containing Fc-domains within 4 weeks of enrollment;
    • Experimental agents within 3 half-lives prior to enrollment, unless progression is documented on therapy;
    • Prior BCMA-directed investigational agents at any time;
    • Prior cell or gene therapy, excluding transfers of genetically unmodified autologous cells (e.g., Hematopoietic stem cell transplantation), at any time; or prior allogeneic HSCT at any time. 
  • Pregnant or breastfeeding.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Jeremy Larsen, M.D.

Closed for enrollment

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

Jacksonville, Fla.

Mayo Clinic principal investigator

Sikander Ailawadhi, M.D.

Closed for enrollment

Contact information:

Cancer Center Clinical Trials Referral Office

(855) 776-0015

More information

Publications

Publications are currently not available
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CLS-20460827

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