A Study Evaluating the Safety, Pharmacokinetics, and Activity of Cevostamab in Participants With Relapsed or Refractory Multiple Myeloma

Multiple Myeloma Clinical Trial

— CAMMA 1  

Official title:

An Open-Label, Multicenter, Phase Ib Trial Evaluating the Safety, Pharmacokinetics, and Activity of Cevostamab as Monotherapy and Cevostamab Plus Pomalidomide and Dexamethasone or Cevostamab Plus Daratumumab and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04910568
• Other study ID #: GO42552
• Secondary ID: 2021-000238-33
• Status: Recruiting
• Phase: Phase 1
• Start date: July 26, 2021
• Est. completion date: July 15, 2025

Study information

• Verified date: June 2024
• Source: Genentech, Inc.
• Contact: Reference Study ID Number: GO42552 https://forpatients.roche.com
• Phone: 888-662-6728 (U.S. and Canada)
• Email: global-roche-genentech-trials[@]gene.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This Phase Ib, multicenter, open-label study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of cevostamab monotherapy, cevostamab plus pomalidomide and dexamethasone (Pd) or cevostamab plus daratumumab and dexamethasone (Dd) which will be administered to participants with relapsed or refractory multiple myeloma (R/R MM) via intravenous (IV) infusion.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 184
• Est. completion date: July 15, 2025
• Est. primary completion date: September 11, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1
• Life expectancy of at least 12 weeks
• Agreement to provide bone marrow biopsy and aspirate samples
• Resolution of adverse events from prior anti-cancer therapy to Grade <=1
• Measurable disease
• For women of childbearing potential: agreement to remain abstinent or use contraception, during the treatment period (including treatment interruptions) and for at least 5 months after the last dose of cevostamab and at least 3 months after the last dose of tocilizumab was administered
• For men: agreement to remain abstinent or use a condom, and agreement to refrain from donating sperm, during the treatment period, and for at least 2 months after the last dose of tocilizumab was administered to avoid exposing the embryo and sexual partner Additional Arm A-Specific Inclusion Criteria
• Diagnosis of R/R MM for which no established therapy for MM is appropriate and available, or intolerance to those established therapies Additional Arm B-Specific Inclusion Criteria
• For Cohort B1S: Participants with R/R MM who have received at least two prior lines of treatment
• For Cohort B2S and additional cohorts: Participants with R/R MM who have received at least 1 prior line of treatment
• Agreement to comply with all requirements of the pomalidomide pregnancy prevention program
• For women of childbearing potential: agreement to remain abstinent or use two reliable methods of contraception starting at least 4 weeks prior to, during the treatment period, and for at least 4 weeks after the last dose of pomalidomide was administered
• For men: agreement to remain abstinent or use a condom during the treatment period and for at least 4 weeks after the last dose of pomalidomide, (even if he has undergone a successful vasectomy) and agreement to refrain from donating sperm and blood during this same period Additional Arm C-Specific Inclusion Criteria
• For Cohort C1S: Participants with R/R MM who have received at least two prior lines of treatment
• For Cohort C2S and additional cohorts: Participants with R/R MM who have received at least 1 prior line of therapy
• For women of childbearing potential: agreement to remain abstinent or use contraceptive methods during the treatment period and for at least 102 days after the last dose of daratumumab was administered
• For men: agreement to remain abstinent or use a condom during the treatment period and for at least 102 days after the last dose of daratumumab was administered to avoid exposing the embryo, and agreement to refrain from donating sperm during this same period

Exclusion Criteria:

• Prior treatment with cevostamab or another agent targeting FcRH5
• Inability to comply with protocol-mandated hospitalization and activities restrictions
• Pregnant or breastfeeding, or intending to become pregnant during the study or within 5 months after the last dose of cevostamab or within 3 months after the last dose of tocilizumab (if applicable).
• Prior use of any monoclonal antibody, radioimmunoconjugate, or antibody-drugconjugate as anti-cancer therapy within 4 weeks before first study treatment, except for the use of non-myeloma therapy
• Prior treatment with systemic immunotherapeutic agents, including, but not limited to, cytokine therapy and anti-CTLA4, anti-PD-1, and antiPD-L1 therapeutic antibodies within 12 weeks or 5 half-lives of the drug, whichever is shorter, before first study treatment
• Prior treatment with chimeric antigen receptor T (CAR T)-cell therapy within 12 weeks before first study treatment
• Treatment with radiotherapy within 4 weeks (systemic radiation) or 14 days (focal radiation) prior to first study treatment
• Treatment with any chemotherapeutic agent or other anti-cancer agent (investigational or otherwise) within 4 weeks or 5 half-lives of the drug, whichever is shorter, prior to first study treatment
• Autologous SCT within 100 days prior to first study treatment
• Prior allogeneic stem cell transplant(ation) (SCT)
• Circulating plasma cell count exceeding 500/micro L or 5% of the peripheral blood white cells
• Prior solid organ transplantation
• History of autoimmune disease
• History of confirmed progressive multifocal leukoencephalopathy
• History of severe allergic or anaphylactic reactions to monoclonal antibody therapy
• Known history of amyloidosis
• Lesions in proximity of vital organs that may develop sudden decompensation/deterioration in the setting of a tumor flare
• History of other malignancy within 2 years prior to screening
• Known treatment-related, immune-mediated adverse events associated with prior checkpoint inhibitors
• Current or past history of central nervous system (CNS) disease, such as stroke, epilepsy, CNS vasculitis, neurodegenerative disease, or CNS involvement by MM
• Significant cardiovascular disease
• Symptomatic active pulmonary disease or requiring supplemental oxygen
• Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection
• Known or suspected chronic active Epstein-Barr virus (EBV) infection
• Recent major surgery within 4 weeks prior to first study treatment
• Positive serologic or PCR test results for acute or chronic hepatitis B virus (HBV) infection
• Acute or chronic hepatitis C virus (HCV) infection
• Known history of Grade >= 3 CRS or immune effector cell-associated neurotoxicity syndrome (ICANS) with prior bispecific therapies
• Known history of hemophagocytic lymphohistiocytosis (HLH) or macrophage activation syndrome (MAS)
• Active symptomatic coronavirus disease 2019 (COVID-19) infection at study enrollment or requiring treatment with intravenous (IV) antiviral where the last dose of IV antiviral treatment was given within 14 days prior to first study treatment. Patients with active COVID-19 infection must have clinical recovery and two negative antigen tests at least 24 hours apart prior to first study treatment
• Positive and quantifiable EBV polymerase chain reaction (PCR) or Cytomegalovirus (CMV) PCR prior to first study treatment
• Known history of HIV seropositivity
• Administration of a live, attenuated vaccine within 4 weeks before first study treatment or anticipation that such a live attenuated vaccine will be required during the study
• Treatment with systemic immunosuppressive medications, with the exception of corticosteroid treatment <=10 mg/day prednisone or equivalent, within 2 weeks prior to first study treatment
• History of illicit drug or alcohol abuse within 12 months prior to screening, in the investigator's judgment Additional Arm B-Specific Exclusion Criteria
• Pregnant or breastfeeding, or intending to become pregnant 4 weeks prior to initiation of study treatment, during the study, (including treatment interruptions) or within 4 weeks after the last dose of pomalidomide
• Significant cardiovascular disease (such as, but not limited to, New York Heart Association Class III or IV cardiac disease, myocardial infarction within the last 12 months, uncontrolled arrhythmias, or unstable angina)
• History of erythema multiforme, Grade >=3 rash, blistering, or severe hypersensitivity to prior treatment with immunomodulatory drugs such as thalidomide, lenalidomide, or pomalidomide
• Inability to tolerate thromboprophylaxis, or contraindication to thromboprophylaxis
• GI disease that might significantly alter absorption of oral drugs Additional Arm C-Specific Exclusion Criteria
• Pregnant or breastfeeding, or intending to become pregnant during the study or within 102 days after the last dose of daratumumab
• Known hypersensitivity to biopharmaceuticals produced in CHO cells or any component of daratumumab formulations
• Known chronic obstructive pulmonary disease (COPD) with a forced expiratory volume in 1 second (FEV1) <50% of predicted normal
• Known moderate or severe persistent asthma within the past 2 years, or current uncontrolled asthma of any classification

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell

Intervention

Drug:
• Cevostamab
Cevostamab will be administered intravenously on a 28-day cycle, up to a total of 13 cycles (Arm A), in 28-day cycles Q2W followed by Q4W (Arm B) and in 21 day cycles from C1-C8 Q3W and 28-day cycles from C9 onwards Q4W (Arm C). For Arm A, participants have the option to enter re-treatment after Cycle 13. For Arms B and C, participants can be treated until disease progression or unacceptable toxicity.
• Tocilizumab
Tocilizumab will be administered for the treatment of cytokine release syndrome (CRS) when necessary.
• Pomalidomide
Pomalidomide will be administered orally (PO) on a 28-day cycle.
• Daratumumab
Daratumumab will be administered subcutaneously (SC) on 21 day (C1-8) and 28-day cycles (C9 onwards).
• Dexamethasone
Arm A: Dexamethasone will be administered as a premedication. Arms B and C: Dexamethasone will be administered via IV or orally at 20 mg as study investigational medicinal product.

Locations

Country	Name	City	State
Australia	Peter MacCallum Cancer Centre; Department of Haematology	Melbourne	Victoria
Australia	The Alfred Hospital; Malignant Haematology & Stem Cell Transplant Service	Melbourne	Victoria
Canada	Hamilton Health Sciences	Hamilton	Ontario
Canada	University Health Network; Princess Margaret Hospital; Medical Oncology Dept	Toronto	Ontario
Czechia	Fakultni Nemocnice Ostrava; Klinika hematoonkologie FNO a LF OU	Ostrava
Czechia	I Interni klinika; Vseobecna fakultni nemocnice	Prague 2
Denmark	Rigshospitalet; Hæmatologisk Klinik, Klinisk Afprøvnings Team KAT	København Ø
France	Hôpital Saint-Louis; Service d'Hématologie	Paris
France	CHU de Poitiers - La Miletrie; Oncologie hematologique - Pole Regional de Cancerologie	Poitiers
France	CHU Pontchaillou; Service Hématologie	Rennes
Israel	Rambam Medical Center; Heamatology & Bone Marrow Transplantation	Haifa
Israel	Sourasky Medical Centre	Tel-Aviv
Italy	ASST PAPA GIOVANNI XXIII; Ematologia	Bergamo	Lombardia
Italy	A.O. Spedali Civili Di Brescia-P.O. Spedali Civili;U.O. Ematologia	Brescia	Lombardia
Japan	National Hospital Organization Okayama Medical Center	Okayama
Japan	The Cancer Institute Hospital of JFCR	Tokyo
Japan	Yamagata University Hospital	Yamagata
Korea, Republic of	Samsung Medical Center	Seoul
Korea, Republic of	Seoul National University Hospital	Seoul
Poland	Uniwersyteckie Centrum Kliniczne; Kilnika Hematologii i Transplantologii, Oddzia? Wczesnych Faz	Gda?sk
Poland	Pratia Onkologia Katowice	Katowice
Poland	Uniwersytecki Szpital Kliniczny w Poznaniu; Oddzial Hematologii i Transplantacji Szpiku	Pozna?
Spain	Hospital Universitari Vall d'Hebron; Servicio de Hematologia	Barcelona
Spain	Hospital General Universitario Gregorio Marañon; Servicio de Hematología	Madrid
United Kingdom	University College London Hospitals NHS Foundation Trust; NIHR UCLH Clinical Research Facility	London
United Kingdom	Royal Marsden Hospital; Academic Dept of Haematology	Sutton
United States	Winship Cancer Institute	Atlanta	Georgia
United States	Colorado Blood Cancer Institute (CBCI) at Presbyterian/ St. Luke's Medical Center	Denver	Colorado
United States	Karmanos Cancer Institute.	Detroit	Michigan
United States	City of Hope	Duarte	California
United States	City of Hope - Lennar Foundation Cancer Center	Irvine	California
United States	Washington University School of Medicine	Saint Louis	Missouri

Sponsors (2)

Lead Sponsor	Collaborator
Genentech, Inc.	Hoffmann-La Roche

Countries where clinical trial is conducted

United States,  Australia,  Canada,  Czechia,  Denmark,  France,  Israel,  Italy,  Japan,  Korea, Republic of,  Poland,  Spain,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Recommended Phase II Dose (RP2D)		Baseline up to approximately 4 years
Primary	Percentage of Participants with Adverse Events		Baseline up to approximately 4 years
Primary	Percentage of Dose Interruptions		Baseline up to approximately 4 years
Primary	Percentage of Dose Reductions		Baseline up to approximately 4 years
Primary	Percentage of Dose Intensity		Baseline up to approximately 4 years
Primary	Percentage of Treatment Discontinuation		Baseline up to approximately 4 years
Secondary	Objective Response Rate (ORR)		Baseline up to approximately 4 years
Secondary	Complete Response/Stringent Complete Response (CR/sCR) Rate		Baseline up to approximately 4 years
Secondary	Rate of Very Good Partial Response (VGPR) or Better		Baseline up to approximately 4 years
Secondary	Progression-free Survival (PFS)		Start of study treatment to first date of disease progression or death from any cause, whichever occurs first (up to approximately 4 years)
Secondary	Duration of Response (DOR)		From first partial response (PR) or better until the first date of disease progression or death from any cause, whichever occurs first (up to approximately 4 years)
Secondary	Time to First Response (for Participants who Achieve a Response of Partial Response (PR) or Better)		Baseline up to approximately 4 years
Secondary	Time to Best Response (for Participants who Achieve a Response of PR or Better)		Baseline up to approximately 4 years
Secondary	Minimal Residual Disease (MRD) Negativity		Baseline up to approximately 4 years
Secondary	Overall Survival (OS)		Baseline up until death from any cause (up to approximately 4 years)
Secondary	Serum Concentration of Cevostamab at Specified Timepoints		Cevostamab Pre-Phase (CPP) Day (D) 1 up to approximately 3 years
Secondary	Total Exposure (Area Under the Concentration-time Curve [AUC]) of Cevostamab		CPP D1 up to approximately 4 years
Secondary	Maximum Observed Serum Concentration (Cmax) of Cevostamab		CPP D1 up to approximately 4 years
Secondary	Minimum Observed Serum Concentration (Cmin) of Cevostamab		CPP D1 up to approximately 4 years
Secondary	Clearance of Cevostamab		CPP D1 up to approximately 4 years
Secondary	Volume of Distribution at Steady State of Cevostamab		CPP D1 up to approximately 4 years
Secondary	Number of Anti-drug Antibody (ADAs) Against Cevostamab at Baseline		Baseline
Secondary	Percentage of Participants with ADAs Against Cevostamab During the Study		Up to approximately 4 years
Secondary	Serum Concentration of Pomalidomide		From Cycle 1 Day 1 through Cycle 6 Day 15. Each cycle=28 days
Secondary	Serum Concentration of Daratumumab		From C1D1 until disease progression or unexpected toxicity. Cycles 1-8 are 21 days and Cycle 9 onward are 28 days.