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

Multiple Myeloma Clinical Trial

Official title:

A Phase 1b, Open-Label Study of Eftozanermin Alfa (ABBV-621) in Combination With Bortezomib and Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04570631
• Other study ID #: M20-258
• Secondary ID: 2020-001983-26
• Status: Active, not recruiting
• Phase: Phase 1
• Start date: November 5, 2020
• Est. completion date: July 30, 2024

Study information

• Verified date: June 2024
• Source: AbbVie
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 40
• Est. completion date: July 30, 2024
• Est. primary completion date: July 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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).

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell

Intervention

Drug:
• Eftozanermin alfa
Intravenous (IV) infusion
• Bortezomib
Intravenous (IV) or Subcutaneous (SC) injection
• Dexamethasone
Oral Tablet

Locations

Country	Name	City	State
France	CHRU Lille - Hopital Claude Huriez /ID# 222302	Lille	Nord
France	Institut Paoli-Calmettes /ID# 222307	Marseille	Bouches-du-Rhone
France	CHU de Nantes, Hotel Dieu -HME /ID# 222303	Nantes	Pays-de-la-Loire
France	HCL - Hopital Lyon Sud /ID# 222304	Pierre Benite CEDEX	Rhone
France	Institut Gustave Roussy /ID# 223951	Villejuif Cedex	Val-de-Marne
Germany	Charite Universitaetsklinikum Berlin - Campus Benjamin Franklin /ID# 223014	Berlin
Germany	Universitaetsklinikum Hamburg-Eppendorf /ID# 222258	Hamburg
Germany	Duplicate_Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz /ID# 222372	Mainz	Rheinland-Pfalz
Germany	Duplicate_Universitaetsklinikum Muenster /ID# 222504	Muenster	Nordrhein-Westfalen
Italy	Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRCCS /ID# 223839	Meldola
Italy	Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Universita Cattolica /ID# 223224	Rome	Lazio
Japan	National Cancer Center Hospital East /ID# 239436	Kashiwa-shi	Chiba
Japan	Nagoya City University Hospital /ID# 222408	Nagoya shi	Aichi
Spain	Hospital Duran i Reynals /ID# 222329	Hospitalet de Llobregat	Barcelona
United States	Emory University, Winship Cancer Institute /ID# 222922	Atlanta	Georgia
United States	Dana-Farber Cancer Institute /ID# 222174	Boston	Massachusetts
United States	University of Texas Southwestern Medical Center /ID# 223811	Dallas	Texas
United States	Duke University Medical Center /ID# 222166	Durham	North Carolina
United States	Norton Healthcare Pavilion /ID# 222918	Louisville	Kentucky

Sponsors (1)

Lead Sponsor	Collaborator
AbbVie

Countries where clinical trial is conducted

United States,  France,  Germany,  Italy,  Japan,  Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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.	Up to approximately 3 weeks after the first dose of study drug
Primary	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.	Up to approximately 44 weeks after the first dose of study drug
Secondary	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.	Up to approximately 44 weeks after the first dose of study drug
Secondary	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.	Up to approximately 44 weeks after the first dose of study drug
Secondary	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.	Up to approximately 44 weeks after the first dose of study drug
Secondary	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.	Up to approximately 3 weeks after the first dose of study drug
Secondary	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.	Up to approximately 44 weeks after the first dose of study drug
Secondary	Change in Vital Sign Measurements	Change from baseline in vital sign measurements such as systolic and diastolic blood pressure will be assessed.	Up to approximately 44 weeks after the first dose of study drug
Secondary	Electrocardiogram (ECG)	Participants with change from baseline in ECG variables will be assessed.	Up to approximately 44 weeks after the first dose of study drug
Secondary	Number of Participants With Abnormal Clinical Laboratory Test Results	Number of participants with abnormal clinical laboratory test results like hematology will be assessed.	Up to approximately 44 weeks after the first dose of study drug
Secondary	Trough Concentration (Ctrough) of Eftozanermin Alfa	Serum concentration prior to administration of study drug.	Up to Day 106
Secondary	Maximum Serum Concentration (Cmax) of Eftozanermin Alfa	Serum concentration at 15 min after end of infusion.	Up to Day 8
Secondary	Antidrug Antibody (ADA)/Neutralizing Antibody (Nab) Assay	Serum sample assay for ADA/Nab (Nabs will be analyzed only upon request).	Up to approximately 44 weeks after the first dose of study drug