We're building a better ClinicalTrials.gov. Check it out and tell us what you think!
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

HB10101 Multiple Myeloma

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04720313
Recruitment Status : Recruiting
First Posted : January 22, 2021
Last Update Posted : January 22, 2021
Sponsor:
Information provided by (Responsible Party):
Polina Stepensky, Hadassah Medical Organization

Study Description
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
It is a phase one study with dose escalation and safety CART in BCMA- Expressing Multiple Myeloma Patients

Condition or disease Intervention/treatment Phase
Dose Escalation and Safety Drug: CART BCMA Phase 1

Detailed Description:

The intention with HBI0101 CART is to follow the chimeric antigen receptor T-cells (CART) approach, as for approved products, but target the B cell maturation antigen (BCMA) rather than the CD19 antigen targeted by KYMRIAHTM (tisagenlecleucel) and YESCARTATM (axicabtagene ciloleucel).

Importantly, successful results from at least three clinical trials of a BCMA targeted CAR T therapy were published (Zhao 2018, Brundo 2018, Raje 2019), with excellent results obtained for relapsed or refractory multiple myeloma (MM) patients, that validate the approach. The CAR vector employed for HBI0101 CART is almost identical to the vector employed for the clinical study reported by Raje 2019, therefore, a strong therapeutic response is expected also for HBI0101 CART together with a similar manageable safety profile

Study Design
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 48 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description: Multiple Myeloma Patients
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1 Dose Escalation and Safety Study of HBI0101 CART in BCMA-Expressing
Actual Study Start Date : January 1, 2021
Estimated Primary Completion Date : January 2023
Estimated Study Completion Date : January 2026

Resource links provided by the National Library of Medicine


Arms and Interventions
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Arm Intervention/treatment
Experimental: CART BCMA
The dose escalation phase (Part A) will include the following doses of CAR-positive (CAR+) T cells: 150×10^6, 450×10^6, 800×10^6 or 1200 ×10^6 The expansion phase (Part B) will include a dose between 450×10^6 to 800×10^6 CAR-positive (CAR+) T cells
 Drug: CART BCMA
HBI0101 CART is defined as autologous T cells transduced ex-vivo with anti-BCMA CAR retroviral vector encoding the chimeric antigen receptor (CAR) targeted to human BCMA. The HBI0101 CART is provided fresh without cryopreservation.


Outcome Measures
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. Determination of MTD [ Time Frame: 21 days ]
    Part A: Determination of MTD Part B: Confirmation of selected dose tested (at or below MTD) ( safety )


Secondary Outcome Measures :
  1. The overall survival [ Time Frame: 2 years ]
    according to the IMWG Uniform Response Criteria for Multiple Myeloma

  2. The progression-free survival [ Time Frame: 2 years ]
    according to the IMWG Uniform Response Criteria for Multiple Myeloma


Eligibility Criteria
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 120 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • ≥18 years of age

    • Voluntarily signed informed consent form (ICF)
    • Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2
    • Diagnosis of MM with relapsed or refractory disease and have had at least 3 different prior lines of therapy including proteasome inhibitor, immunomodulatory therapy and at least one antibody therapy.

    • Subjects must have measurable disease, including at least one of the criteria below:

      • Serum M-protein greater or equal to 0.5 g/dL
      • Urine M-protein greater or equal to 200 mg/24 h
      • Serum free light chain (FLC) assay: involved FLC level greater or equal to 5 mg/dL (50 mg/L) provided serum FLC ratio is abnormal
      • A biopsy-proven evaluable plasmacytoma
      • Bone marrow plasma cells > 20% of total bone marrow cells
      • Non secretory patient will be allowed provided they have measurable disease by PET-CT or bone marrow aspiration, as designated.
    • Women of child-bearing potential (WCBP), must have a negative serum pregnancy test prior to treatment. All sexually active WCBP and all sexually active male subjects must agree to use effective methods of birth control throughout the study
    • Recovery to ≤Grade 2 or baseline of any non-hematologic toxicities due to prior treatments, excluding alopecia and Grade 3 neuropathy
    • Ability and willingness to adhere to the study visit schedule and all protocol requirements
Contacts and Locations
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04720313


Contacts
Layout table for location contacts
Contact: Polina Stepensky, Prof 972-26777803 polina@hadassah.org.il
Contact: Liliane DRAY, NSC 97226777260 lilane@hadassah.org.il

Locations
Layout table for location information
Israel
Hadassah University Hospital Recruiting
Jerusalem, Israel, 91120
Contact: Polina Stepensky, Prof    972-26777803    polina@hadassah.org.il   
Contact: liliane Dray, NSC    972-26777260    lilane@hadassah.org.il   
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Layout table for investigator information
Principal Investigator: Polina Stepensky, prof. Hadassah university hospital of Jerusalem
More Information
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Layout table for additonal information
Responsible Party: Polina Stepensky, Professor, Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT04720313    
Other Study ID Numbers: MOH_2020-12-22_009584
First Posted: January 22, 2021    Key Record Dates
Last Update Posted: January 22, 2021
Last Verified: January 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: There will be no IPD sharing

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No