Study to Determine Recommended Phase 2 Dose of Intravenous (IV) Eftozanermin Alfa in Combination With IV or Subcutaneous (SC) Bortezomib and Oral Dexamethasone Tablet and to Assess Change in Disease Symptoms in Adult Participants With Relapsed or Refractory Multiple Myeloma

Phase 1TerminatedNCT04570631

AbbVie4 enrolled

Overview

Multiple myeloma (MM) is a rare cancer caused by abnormal survival of plasma cells (blood cells). Most trial participants with MM relapse (cancer has come back) or become non- responsive to treatment and remission gets shorter after each line of treatment. This is a study to determine recommended Phase 2 dose and change in disease symptoms of eftozanermin alfa in combination with bortezomib and dexamethasone to assess how efficient the treatment is in adult participants with relapsed/refractory (R/R) MM. Eftozanermin alfa (ABBV-621) is an investigational drug being developed for the treatment of R/R Multiple Myeloma (MM). Study doctors put the participants in 1 of the 2 groups, called treatment arms. Each group receives a different treatment. Participants in one arm will receive different doses of eftozanermin alfa in combination with bortezomib and dexamethasone to determine phase 2 dose (RP2D). Participants in the other arm will receive eftozanermin alfa at RP2D in combination with bortezomib and dexamethasone. Around 40 adult participants with relapsed/refractory multiple myeloma will be enrolled at approximately 20 sites across the world. Participants will receive eftozanermin alfa as an infusion into the vein in combination with bortezomib as an infusion into the vein or an injection under the skin and oral dexamethasone tablets for 12 cycles. Each cycle is 21 days for cycles 1-8 and 35 days for cycles 9-12. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Documented diagnosis of multiple myeloma (MM) based on standard International Myeloma Working Group (IMWG) criteria. * Has measurable disease at screening, defined by at least 1 of the following: * Serum M-protein \>= 1.0 g/dL (\>= 10 g/L); OR * Urine M-protein \>= 200 mg/24 hours; OR * Serum free light chain (sFLC) \>= 10 mg/dL (100 mg/L), provided serum FLC ratio is abnormal. * Relapsed or refractory MM after receiving at least 3, but no more than 6 prior lines of therapy, including an immunomodulatory agent (IMiD), proteasome inhibitor (PI), and an anti-CD38 antibody, and has documented disease progression that occurred during or after the most recent therapy. * Has adequate hematologic, hepatic and renal function as defined in the protocol. * Eastern Cooperative Oncology Group (ECOG) 0 or 1. * Life expectancy \>= 12 weeks. Exclusion Criteria: * Received bortezomib as part of the most recent prior therapy. * Has primary refractory disease defined as disease that is non-responsive. * Has not achieved a minimal response or better per IMWG criteria with any therapy. * Has discontinued bortezomib due to toxicity. * History of chronic liver disease or significant unresolved liver disease; currently active (within the last 6 months) hepatic impairment according to Child-Pugh Classification B or C. * History of cataract surgery within 6 months prior to study treatment and participant is not anticipated to have cataract surgery during the study treatment period (as assessed by ophthalmological exam at baseline). * Evidence of (as assessed by ophthalmological exam at baseline) uveitis, neovascular age related macular degeneration, retinal vein or artery occlusion and/or macular edema; no evidence of moderate or worsening diabetic retinopathy, retinal vascular disease or glaucoma (including participants with history of developing increased intraocular pressure after corticosteroid treatment) per clinical discretion of the consulting eye specialist. * Peripheral neuropathy Grade \>= 2 or Grade 1 with pain. * Receipt of one of the following: * Corticosteroids at a dose equivalent to \> 4 mg daily of dexamethasone or a single dose of \> 40 mg of dexamethasone within 2 weeks prior to first dose. * Monoclonal antibodies used for multiple myeloma treatment within 4 weeks prior to first dose of study treatment. * Any other systemic therapies used for multiple myeloma treatment within 5 half-lives or 2 weeks prior to first dose, whichever is longer (or 2 weeks if half-life is unknown).

Locations (19)

Duplicate_Emory University, Winship Cancer Institute /ID# 222922

Atlanta, Georgia, United States

Norton Healthcare Pavilion /ID# 222918

Louisville, Kentucky, United States

Dana-Farber Cancer Institute /ID# 222174

Boston, Massachusetts, United States

Duke University Medical Center /ID# 222166

Durham, North Carolina, United States

University of Texas Southwestern Medical Center /ID# 223811

Dallas, Texas, United States

Institut Paoli-Calmettes /ID# 222307

Marseille, Bouches-du-Rhone, France

CHRU Lille - Hopital Claude Huriez /ID# 222302

Lille, Nord, France

CHU de Nantes, Hotel Dieu -HME /ID# 222303

Nantes, Pays de la Loire Region, France

HCL - Hopital Lyon Sud /ID# 222304

Pierre-Bénite, Rhone, France

Institut Gustave Roussy /ID# 223951

Villejuif, Val-de-Marne, France

...and 9 more locations

Outcomes

Primary Outcomes

Recommended Phase 2 Dose (RP2D) of Eftozanermin Alfa in Combination With Bortezomib and Dexamethasone (Safety Lead-In Arm)

RP2D of eftozanermin alfa in combination with bortezomib and dexamethasone will be determined.

Time frame: Up to approximately 3 weeks after the first dose of study drug

Objective Response Rate (ORR) (Dose Expansion Arm)

ORR is defined as percentage of participants with a response of partial response (PR) or better per International Myeloma Working Group (IMWG) criteria.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Secondary Outcomes

Rate of Very Good Partial Response (VGPR) or Better per IMWG Criteria

Percentage of participants with a response of VGPR or better per IMWG criteria will be assessed.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Duration of Response (DOR) for ORR

DOR for ORR is defined as the number of days from the date of first response (PR or better) to the date of first occurrence of progressive disease (PD) or death from any cause, whichever occurs first.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Duration of Response (DOR) for VGPR or Better

DOR for VGPR or better rate is defined as the number of days from the date of first response (VGPR or better) to the date of first occurrence of PD or death from any cause, whichever occurs first.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Number of Participants With Dose-Limiting Toxicities (DLTs)

DLTs are any of the hematologic, nonhematologic toxicities, adverse events (AEs) occurring following administration of study drug as described in the protocol and evaluated by the Investigator and the sponsor.

Time frame: Up to approximately 3 weeks after the first dose of study drug

Number of Participants With Adverse Events (AEs)

An adverse event (AE) is defined as any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment. The investigator will assess the relationship of each event to the use of study drug as being of reasonable possibility or no reasonable possibility. A serious adverse event (SAE) is an event that results in death, is life-threatening, requires or prolongs hospitalization, results in a congenital anomaly, persistent or significant disability/incapacity or is an important medical event that, based on medical judgment, may jeopardize the subject and may require medical or surgical intervention to prevent any of the outcomes listed above.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Change in Vital Sign Measurements

Change from baseline in vital sign measurements such as systolic and diastolic blood pressure will be assessed.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Electrocardiogram (ECG)

Participants with change from baseline in ECG variables will be assessed.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Number of Participants With Abnormal Clinical Laboratory Test Results

Number of participants with abnormal clinical laboratory test results like hematology will be assessed.

Time frame: Up to approximately 44 weeks after the first dose of study drug

Trough Concentration (Ctrough) of Eftozanermin Alfa

Serum concentration prior to administration of study drug.

Time frame: Up to Day 106

Maximum Serum Concentration (Cmax) of Eftozanermin Alfa

Serum concentration at 15 min after end of infusion.

Time frame: Up to Day 8

Antidrug Antibody (ADA)/Neutralizing Antibody (Nab) Assay

Serum sample assay for ADA/Nab (Nabs will be analyzed only upon request).

Time frame: Up to approximately 44 weeks after the first dose of study drug

Study to Determine Recommended Phase 2 Dose of Intravenous (IV) Eftozanermin Alfa in Combination With IV or Subcutaneous (SC) Bortezomib and Oral Dexamethasone Tablet and to Assess Change in Disease Symptoms in Adult Participants With Relapsed or Refractory Multiple Myeloma

Overview

Conditions

Interventions

Eligibility

Locations (19)

Outcomes

Primary Outcomes

Secondary Outcomes