Marizomib Central Nervous System (CNS)

July 15, 2024 updated by: Clifton Mo, MD, Dana-Farber Cancer Institute

A Phase 2 Study With Safety Run-In of Marizomib, Pomalidomide, and Dexamethasone For Relapsed and Refractory Multiple Myeloma and CNS Myeloma

This research is being done to test whether the investigational drug marizomib is safe and effective when used in combination with standard of care drugs for the treatment of multiple myeloma.

Study Overview

Status

Withdrawn

Conditions

Intervention / Treatment

Detailed Description

This is a Phase 2 single-arm study, incorporating two cohorts and using the combination of marizomib plus pomalidomide and dexamethasone in relapsed/refractory multiple myeloma (RRMM) patients and in RRMM patients with CNS involvement.

This research study involves a three drug chemotherapy regimen which includes taking the study drug marizomib, as well as pomalidomide and dexamethasone. The U.S. Food and Drug Administration (FDA) has not approved marizomib as a treatment for any disease. The U.S. Food and Drug Administration (FDA) has approved pomalidomide and dexamethasone as a treatment option for multiple myeloma.

The research study procedures include screening for eligibility and study treatment including evaluations and follow up visits. As the study is looking for the highest dose of the study drug that can be administered safely without severe or unmanageable side effects in participants that have multiple myeloma, not everyone who participates in this research study will receive the same dose of the study drug. The dose received will depend on the number of participants who have been previously enrolled in the study and how well participants have tolerated their doses. Participants will receive study treatment for as long as participants do not have serious side effects and their disease does not get worse.

It is expected that about 48 people will take part in this research study.

Bristol-Myers Squibb is supporting this research study by providing funding and study drug.

Study Type

Interventional

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Massachusetts
      • Boston, Massachusetts, United States, 02115
        • Dana-Farber Cancer Institute
      • Boston, Massachusetts, United States, 02114
        • Massachusetts General Hospital Cancer Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Previously diagnosed with MM based on standard IMWG criteria and currently requires treatment.
  • Patients in the CNS-involved cohort must have CNS involvement of MM as defined by meningeal myelomatosis and/or radiological evidence of leptomeningeal disease and/or intracranial plasmacytoma involving brain parenchyma.
  • Patients in the CNS-involved cohort must have received at least one or more previous lines of therapy including an IMiD and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy.
  • Patients in the RRMM cohort must have received at least two or more previous therapies including lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or within 60 days of completion of the last therapy.

  • Patients in the RRMM cohort must have measurable disease defined as at least one of the following:

    • Serum M protein ≥ 0.5 g/dL (≥5 g/L)
    • Urine M protein ≥200 mg/24 hours
    • Serum free light chain (FLC) assay: Involved FLC assay ≥10 mg/dL (≥100 mg/L) and an abnormal serum FLC ratio (<0.26 or >1.65)

  • Screening Laboratory evaluations within the following parameters

    • Absolute neutrophil count (ANC) ≥ 1,000 cells/dL (1.0 x 109/L) (Growth factors cannot be used within 14 days before first drug administration)
    • Platelet count ≥ 75,000 cells/dL (75 x 109/L) (without transfusions required during the 14 days prior to initiation of therapy)
    • Hemoglobin ≥ 8.0 g/dl (RBC transfusions are permitted)
    • Total Bilirubin ≤ 1.5 X upper limit of normal (ULN) (except subjects with Gilbert Syndrome, who can have total bilirubin < 3.0 mg/dL)
    • AST (SGOT) and ALT (SGPT) ≤ 3.0 x ULN
    • Calculated creatinine clearance ≥ 45 mL/min
  • ECOG performance status ≤2 (Karnofsky ≥60%, see Appendix A)
  • All study participants must be registered into the mandatory POMALYST REMS® program, and be willing and able to comply with the requirements of the POMALYST REMS® program.
  • Females of reproductive potential must adhere to the scheduled testing as required in the POMALYST REMS® program.
  • Able to take aspirin (81 or 325 mg) daily as prophylactic anticoagulation (patients intolerant to ASA may use warfarin or low molecular weight heparin).
  • Patients have given voluntary written informed consent before performance of any study-related procedures not part of normal medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to their future medical care.
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

  • Prior exposure to marizomib. and primary refractoriness to pomalidomide or a pomalidomide combination. Prior pomalidomide exposure is permitted but patients must have shown tolerance (defined as no grade 3 or greater non-hematologic toxicity), as well as responsiveness to pomalidomide-based therapy (defined as MR or better).
  • Diagnosed or treated for another malignancy within 3 years prior to enrollment, with the exception of complete resection of basal cell carcinoma or squamous cell carcinoma of the skin, an in situ malignancy, or low risk prostate cancer after curative therapy/watchful waiting.
  • Known GI disease or GI procedure that could interfere with the oral absorption of pomalidomide including difficulty swallowing.
  • Systemic treatment, within 14 days before the first dose of pomalidomide, with strong CYP3A inducers (rifampin, rifapentine, rifabutin, carbamazepine, phenytoin, phenobarbital), or use of St. John's wort.
  • Peripheral neuropathy ≥ Grade 3, or Grade 2 with pain on clinical examination during the screening period.
  • Any medical or psychiatric illness that in the investigator's opinion, would impose excessive risk to the patient or would adversely affect his/her participating in this study.
  • Current uncontrolled cardiovascular conditions, including uncontrolled hypertension, uncontrolled cardiac arrhythmias, symptomatic congestive heart failure, unstable angina, Grade 3 thromboembolic event or myocardial infarction within the past 6 months.
  • The following therapies within the stated time frames prior to initiation of therapy: previous cytotoxic therapies, including cytotoxic investigational agents, for MM within 3 weeks; IMiDs, PIs, corticosteroids, other approved therapeutics and monoclonal antibodies (Mabs) within 2 weeks; and investigational therapies within 4 weeks. Please note consideration of the interval for investigational agents from already approved classes of drug in MM (e.g. Cell-Mods, Mabs) can be considered on a case by case basis with the PI. Prior peripheral stem cell transplant within 12 weeks and the use of live vaccines within 30 days.
  • Prior allogeneic stem cell transplantation with active graft-versus-host-disease (grade 2 or greater).
  • Prior major surgical procedure or radiation therapy within 4 weeks of initiation of therapy (this does not include limited course of radiation used for management of bone pain within 7 days of initiation of therapy).
  • Daily requirement for corticosteroids equivalent to > 10 mg/day prednisone, except for inhalation corticosteroids, for the RRMM cohort. For patients with CNS involvement who require a higher dose of corticosteroids for control of vasogenic edema (e.g. 16 mg/day dexamethasone), eligibility will be determined on a case-by-case basis after discussion with the PI.
  • Any > Grade 1 adverse reaction unresolved from previous treatments according to the National Cancer Institute - Common Terminology Criteria for Adverse Events Version 5.0 (NCI CTC AE v.5.0). The presence of alopecia any grade or peripheral neuropathy ≤ Grade 2 without pain is allowed.
  • Concurrent symptomatic amyloidosis or plasma cell leukemia.
  • POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein and skin changes).
  • Known active infection requiring parenteral or oral anti-infective treatment within 7 days of start of therapy.
  • Known human immunodeficiency virus or active hepatitis C viral infection.

  • Active hepatitis B viral infection (defined as HBsAg+).

    • Patients with prior hepatitis B vaccine are permitted (defined as HBsAg-, Anti-HBs+, Anti-HBc-).
    • Non-active hepatitis B (HBsAg-, Anti-HBs+, Anti-HBc+) may be enrolled at the discretion of the investigator after consideration of risk of reactivation.
  • Pregnant or breast-feeding females.
  • Participants who are receiving any other investigational agents.
  • History of erythema multiforme or severe hypersensitivity to prior IMiD's®.
  • Inability to tolerate thromboprophylaxis.
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • Known hypersensitivity to thalidomide or lenalidomide or other drugs included in this study.

The development of erythema nodosum if characterized by a desquamating rash while taking thalidomide, lenalidomide, pomalidomide or similar drugs.

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Marizomib plus pomalidomide and dexamethasone

A safety run-in using a modified 3+3 dose de-escalation design with relapsed/refractory multiple myeloma (RRMM) cohort, expanded to a total of 16 participants once recommended phase 2 does (RP2D) has been identified.

  • Marizomib (MRZ) at a pre-determined dose on Days 1, 8, 15, 22 of a 28 day study cycle
  • Pomalidomide (POM) at a daily predetermined dose on Days 1-21 of a 28 day study cycle
  • Dexamethasone (DEX) at a daily predetermined dose on Days 1, 2, 8, 9, 15, 16, 22, 23 of a 28 day study cycle

Simultaneously, relapsed/refractory multiple myeloma (RRMM) with central nervous system (CNS) involvement cohort will receive an identical modified 3+3 dose de-escalation design and expanded to an efficacy-evaluable total of 30 patients once recommended phase 2 does (RP2D has been identified
Drug: Marizomib
Intravenous Infusion
Other Names:
  • Salinosporamide A
Drug: Pomalidomide
Taken orally
Other Names:
  • Pomalyst
Drug: Dexamethasone
Taken orally
Other Names:
  • Decadron
  • Hexadrol
  • Dexasone
  • Maxidex

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximum Tolerated Dose (MTD) Safety Run-In
Time Frame: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
MTD is defined as the highest dose level where no patients (of the 6 treated) develop a dose limiting toxicity (DLT)
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Dose Limiting Toxicity (DLT)
Time Frame: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Toxicity summaries will be stratified by dose level, grade, and treatment attribution
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
The number and proportion of adverse events, graded as defined by CTCAE version 5.0.
Time Frame: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
CTCAE version 5.0.
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Overall response rate (ORR)
Time Frame: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Assessed using the updated International Myeloma Working Group Response Criteria (IMWG) (Rajkumar 2011).
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time to response (TTR)
Time Frame: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Assessed using the updated International Myeloma Working Group Response Criteria (IMWG) (Rajkumar 2011).
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Progression free survival (PFS)
Time Frame: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first. up to 5 years
Assessed using the updated International Myeloma Working Group Response Criteria
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first. up to 5 years
Duration of response (DOR)
Time Frame: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Assessed using the updated International Myeloma Working Group Response Criteria (IMWG) (Rajkumar 2011).
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, up to 5 years
Overall survival (OS)
Time Frame: From date of enrollment until date of death from any cause, up to 5 years
Assessed using the updated International Myeloma Working Group Response Criteria
From date of enrollment until date of death from any cause, up to 5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Dana-Farber Cancer Institute

Collaborators

Bristol-Myers Squibb

Investigators

  • Principal Investigator: Clifton Mo, MD, Dana-Farber Cancer Institute

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

March 1, 2024

Primary Completion (Estimated)

December 1, 2025

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

April 14, 2021

First Submitted That Met QC Criteria

September 17, 2021

First Posted (Actual)

September 20, 2021

Study Record Updates

Last Update Posted (Actual)

July 16, 2024

Last Update Submitted That Met QC Criteria

July 15, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 20-551

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The Dana-Farber / Harvard Cancer Center encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: [contact information for Sponsor Investigator or designee]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research.

IPD Sharing Time Frame

Data can be shared no earlier than 1 year following the date of publication

IPD Sharing Access Criteria

Contact the Belfer Office for Dana-Farber Innovations (BODFI) at innovation@dfci.harvard.edu

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Multiple Myeloma

Clinical Trials on Marizomib

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in United Kingdom

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe