BT062 in Combination With Lenalidomide or Pomalidomide and Dexamethasone in Patients With Multiple Myeloma

BT062 is an antibody-drug conjugate designed to bind and destroy Myeloma cells. The study drug is being given in multiple doses with standard Multiple Myeloma treatments, lenalidomide and dexamethasone, to test how well the treatments are tolerated and work together. This study is a dose escalation study with the purpose to find out the highest dose of BT062 that a subject can tolerate in combination with lenalidomide and dexamethasone.

Inclusion criteria

• Diagnosis of active Multiple Myeloma according to the International Myeloma Working Group (IMWG) diagnostic criteria
• Relapsed or relapsed/refractory progressive Multiple Myeloma
• Subjects who failed at least one prior therapy (BT062/Len/dex)
• Subjects who failed at least two prior therapy (BT062/Pom/dex)
• Subjects age ≥18 years
• Life expectancy of ≥12 weeks
• Eastern Cooperative Oncology Group (ECOG) performance status (Zubrod) ≤2
• Normal organ and bone marrow
• Signed written informed consent in accordance with federal, local, and institutional guidelines
• Subjects must agree to follow all Guidelines from REVLIMID REMS Program or POMALYST REMS
• Women of child bearing potential (WCBP), must agree to use 2 contraceptive methods

Exclusion criteria

• Chemotherapy or radiotherapy within 3 weeks (6 weeks for nitrosoureas or mitomycin C) prior to day 1 or those who have not recovered from adverse events (AEs) due to agents administered more than 3 weeks earlier
• Antineoplastic therapy with biological agents within 2 weeks before day 1 or within 5 drug half-lives (t½) prior to first dose, whichever time period is longer
• Concomitant antineoplastic therapies including chemotherapy, radiotherapy, or biological agents during the study
• Treatment with another investigational drug during the study or within 3 weeks before day 1 or within 5 drug half-live (t½) prior to first dose, whichever time period is longer
• Treatment with BT062 in previous studies
• Major surgery within 4 weeks before day 1 (this does not include placement of vascular access device or tumor biopsies)
• Malignancy within 3 years before day 1, other than the trial indication multiple myeloma and excluding treated non-melanoma skin cancer, superficial bladder cancer, carcinoma in-situ of the cervix and prostate carcinoma ≤ Gleason Grade 6 with stable prostate specific antigen (PSA) levels
• Subjects with plasma cell leukemia (PCL)
• Subjects with deep vein thrombosis (DVT) and Pulmonary embolism (PE) within 3 months prior to day 1 treatment
• Severe infections necessitating use of antibiotics / antivirals during the screening period
• Clinically relevant active infection including active hepatitis B or C or human immunodeficiency virus (HBV, HCV, or HIV) or any other concurrent disease
• Acute or relevant abnormalities in electrocardiogram (ECG)
• Significant cardiac disease
• Pregnant or breast-feeding
• Positive serum or urine pregnancy test
• Hypersensitivity to the active substance or to any of the excipients for study drug BT062, or history of severe allergic or anaphylactic reaction to therapeutic proteins (e.g. reaction to vaccination or to biological therapy)