A Safety and Efficacy Trial of JCAR017 Combinations in Subjects With Relapsed/Refractory B-cell Malignancies

NCT ID: NCT03310619

Last Updated: 2024-04-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 62 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-12-20
• Study Completion Date: 2023-02-15

Brief Summary

This is a global, open-label, multi-arm, parallel multi-cohort, multi-center, Phase 1/2 study to determine the safety, tolerability, PK, efficacy and patient-reported quality of life of JCAR017 in combination with various agents. This protocol is intended to evaluate various drug combinations with JCAR017, as separate arms, over the life of the protocol, using the same objectives. Each combination will be evaluated separately (ie, the intention is not to compare between combinations) for the purposes of the objectives, trial design, and statistical analysis. The following combinations will be tested:

Arm A: JCAR017 in combination with durvalumab Arm B: JCAR017 in combination with CC-122 (avadomide) Arm C: JCAR017 in combination with CC-220 (iberdomide) Arm D: JCAR017 in combination with ibrutinib Arm E: JCAR017 in combination with relatlimab and/or nivolumab Arm F: JCAR017 in combination with CC-99282 Additional arms will be added by way of amendment once combination agents have been selected.

The study will consist of 2 parts: dose finding (Phase 1) and dose expansion (Phase 2). Dose expansion may occur in one or more arms.

Detailed Description

During Phase 1, different arms may be opened to test JCAR017 in combination with combination agent(s) in adult subjects with R/R aggressive B-cell NHL. Within each arm, different doses and schedules of JCAR017 and the combination agent(s) may be tested in several cohorts and subcohorts per arm. During Phase 2 of the study, the expansion of any dose level and schedule for any arm that has been shown to be safe may occur.

Arm A will test JCAR017 in combination with Durvalumab Arm B will test JCAR017 in combination with CC-122 Arm C will test JCAR017 in combination with CC-220 (iberdomide ) Arm D will test JCAR017 in combination with ibrutinib. Arm E will test JCAR017 in combination with relatlimab and/or nivolumab Arm F will test JCAR017 in combination with CC-99282 All subjects from Phase 1 and Phase 2 will be followed for 24 months following JCAR017 infusion. Post-study follow-up for survival, relapse, long-term toxicity (including new malignancies), and viral vector safety will continue under a separate long-term follow-up (LTFU) protocol for up to 15 years after the JCAR017 dose as per health authority regulatory guidelines.

Conditions

Lymphoma, Non-Hodgkin; Lymphoma, Large B-Cell, Diffuse; Lymphoma, Follicular

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm A: JCAR017 in combination with Durvalumab

JCAR017 will be administered at a single flat dose of 50 x 10\^6 CAR+T cells or 100 x 10\^6 CAR+T cells. The combination agent will be administered at different doses and/ or schedules

Group Type: EXPERIMENTAL

JCAR017

Intervention Type: BIOLOGICAL

Gene modified autologous T cells

Durvalumab

Intervention Type: DRUG

Anti-PD-L1

Arm B: JCAR017 in combination with CC-122

This arm will test JCAR017 in combination with the CC-122. In adult subjects with R/R aggressive B-cell NHL. JCAR017 will be administered at a dose of 100 x 10\^6 CAR+T cells. The combination agent will be administered at different doses

Group Type: EXPERIMENTAL

JCAR017

Intervention Type: BIOLOGICAL

Gene modified autologous T cells

CC-122

Intervention Type: DRUG

Pleiotropic Pathway Modifier

Arm C: JCAR017 in combination with CC-220

This arm will test JCAR017 in combination with CC-220. In adult subjects with R/R aggressive B-cell NHL. JCAR017 will be administered at a dose of 100 x 10\^6 CAR+T cells. The combination agent will be administered at different doses

Group Type: EXPERIMENTAL

JCAR017

Intervention Type: BIOLOGICAL

Gene modified autologous T cells

CC-220

Intervention Type: DRUG

CC-220

Arm D: JCAR017 in combination with Ibrutinib

This arm will test JCAR017 in combination with ibrutinib. In adult subjects with R/R aggressive B-cell NHL. JCAR017 will be administered at a dose of 100 x 10\^6 CAR+T cells. The combination agent will be administered at a fixed dose of 420 mg daily

Group Type: EXPERIMENTAL

JCAR017

Intervention Type: BIOLOGICAL

Gene modified autologous T cells

Ibrutinib

Intervention Type: DRUG

Ibrutinib

Arm E: JCAR017 in combination with relatlimab and/or nivolumab

This arm will test JCAR017 in combination with relatlimab and/or nivolumab in adult subjects with R/R aggressive B-cell NHL. JCAR017 will be administered at a dose of 100 x 10\^6 CAR+T cells. The combination agent will be administered at different doses and/or schedules

Group Type: EXPERIMENTAL

JCAR017

Intervention Type: BIOLOGICAL

Gene modified autologous T cells

Relatlimab

Intervention Type: DRUG

Relatlimab

Nivolumab

Intervention Type: DRUG

Nivolumab

Arm F: JCAR017 in combination with CC-99282

This arm will test JCAR017 in combination with CC-99282 in adult subjects with R/R aggressive B-cell NHL. JCAR017 will be administered at a dose of 100 x 10\^6 CAR+T cells. The combination agent will be administered at different doses and/or schedules.

Group Type: EXPERIMENTAL

JCAR017

Intervention Type: BIOLOGICAL

Gene modified autologous T cells

CC-99282

Intervention Type: DRUG

CC-99282

Interventions

JCAR017

Gene modified autologous T cells

Intervention Type: BIOLOGICAL

Durvalumab

Anti-PD-L1

Intervention Type: DRUG

CC-122

Pleiotropic Pathway Modifier

Intervention Type: DRUG

Ibrutinib

Ibrutinib

Intervention Type: DRUG

CC-220

CC-220

Intervention Type: DRUG

Relatlimab

Relatlimab

Intervention Type: DRUG

Nivolumab

Nivolumab

Intervention Type: DRUG

CC-99282

CC-99282

Intervention Type: DRUG

Other Intervention Names

MEDI4736

Eligibility Criteria

Inclusion Criteria

1. Subject is ≥ 18 years of age at the time of signing the informed consent form ().

2. Subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted.

3. Subject is willing and able to adhere to the study visit schedule and other protocol requirements.

4. Subject must have aggressive B-cell NHL according to "the 2016 revision of the WHO classification of lymphoid neoplasms", histologically confirmed at last relapse by the treating institution, defined as:

1. Diffuse large B-cell lymphoma (DLBCL) Not otherwise specified (NOS) including transformed indolent Non-Hodgkin lymphoma (NHL)

2. Follicular lymphoma Grade 3B

3. T cell/histiocyte-rich large B-cell lymphoma

4. Epstein-Barr virus (EBV) positive DLBCL, NOS

5. Primary mediastinal (thymic) large B-cell lymphoma

6. High grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements with DLBCL histology (double/triple-hit lymphoma)

5. Subjects disease must have relapsed or be refractory to at least 2 prior lines of therapy. Previous therapy must have included a CD20-targeted agent and an anthracycline.

6. Subject must have

1. Positron emission tomography (PET)-positive (Deauville score 4 or 5) and computed tomography (CT) measurable disease as per Lugano Classification

2. Sum of product of perpendicular diameters (SPD) of up to 6 index lesions ≥ 25 cm2 by CT scan (not applicable to Arm A or B or subjects with Richter's transformation)

7. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1 at screening

8. Adequate organ function

9. Subjects must agree to not donate blood, organs, sperm or semen, and egg cells for usage in other individuals

10. Participants must agree to use effective contraception

Exclusion Criteria

1. Subject has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study based on investigator´s judgment.

2. Subject has any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study based on investigator´s judgment.

3. Subject has any condition that confounds the ability to interpret data from the study based on investigator´s judgment.

4. Subjects with prior history of malignancies, other than aggressive R/R NHL, unless the subject has been free of the disease for ≥ 2 years with the exception of the following non-invasive malignancies:

1. Basal cell carcinoma of the skin

2. Squamous cell carcinoma of the skin

3. Carcinoma in situ of the cervix

4. Carcinoma in situ of the breast

5. Incidental histologic finding of prostate cancer (T1a or T1b using the TNM [tumor, nodes, metastasis] clinical staging system) or prostate cancer that is curative.

6. Other completely resected stage 1 solid tumor with low risk for recurrence

5. Prior treatment with any prior gene therap y product

6. Prior treatment with any adoptive T cell therapy; prior hematopoietic stem cell transplant (HSCT) is allowed

7. Allogeneic HSCT within 90 days of leukapheresis

8. Prior treatment with the combination agent from the assigned arm:

1. Anti PD-1 or PD-L1 (Arm A and E)

2. CC-122 (Arm B)

3. CC-220 (Arm C)

4. Prior treatment with ibrutinib is not exclusionary for subjects on any study arm

5. Anti LAG-3 targeted agent (Arm E)

6. CC-99282 (Arm F)

9. Presence of acute or chronic graft-versus-host disease (GVHD)

10. Presence of the following:

1. Active hepatitis B or active hepatitis C infection

2. History of or active human immunodeficiency virus (HIV) infection

11. Uncontrolled bacterial, viral or fungal infection at the time of leukapheresis, lymphodepleting chemotherapy or JCAR017 infusion

12. Any history of myocarditis (Arm E); history of any one of the following cardiovascular conditions within the past 6 months: Class III or IV heart failure as defined by the New York Heart Association (NYHA), cardiac angioplasty or stenting, myocardial infarction, unstable angina, or other clinically significant cardiac disease (all arms)

13. History or presence of clinically relevant central nervous system (CNS) pathology such as epilepsy, seizure, paresis, aphasia, stroke, severe brain injuries, dementia, Parkinson's disease, cerebellar disease, organic brain syndrome, or psychosis

14. Subjects with active CNS or cerebrospinal fluid (CSF) involvement by malignancy

15. Pregnant or nursing (lactating) women.

16. Subjects with active auto immune disorders/processes or active neurological or inflammatory disorders

17. For subjects to receive oral combination therapy (Arms B, C, D or F): History of a gastrointestinal (GI) condition or procedure that in the opinion of the investigator may affect oral drug absorption.

18. Progressive tumor invasion of venous or arterial vessels.

19. Deep venous thrombosis (DVT)/pulmonary embolism (PE) not managed on a stable regimen of anticoagulation.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Celgene

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Bristol-Myers Squibb

Locations

Local Institution - 011

Duarte, California, United States

Local Institution - 022

Atlanta, Georgia, United States

Local Institution - 014

Chicago, Illinois, United States

Local Institution - 012

Boston, Massachusetts, United States

Local Institution - 021

Boston, Massachusetts, United States

Local Institution - 015

Omaha, Nebraska, United States

Local Institution - 016

Philadelphia, Pennsylvania, United States

Local Institution - 020

Pittsburgh, Pennsylvania, United States

Local Institution - 013

Houston, Texas, United States

Countries

United States

References

Ernst M, Oeser A, Besiroglu B, Caro-Valenzuela J, Abd El Aziz M, Monsef I, Borchmann P, Estcourt LJ, Skoetz N, Goldkuhle M. Chimeric antigen receptor (CAR) T-cell therapy for people with relapsed or refractory diffuse large B-cell lymphoma. Cochrane Database Syst Rev. 2021 Sep 13;9(9):CD013365. doi: 10.1002/14651858.CD013365.pub2.

Reference Type: DERIVED

PMID: 34515338 (View on PubMed)

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Related Links

https://www.bms.com/researchers-and-partners/clinical-trials-and-research.html

BMS Clinical Trial Information

https://www.BMSStudyConnect.com

BMS Clinical Trial Patient Recruiting

Other Identifiers

U1111-1201-2046

Identifier Type: REGISTRY

Identifier Source: secondary_id

JCAR017-BCM-002

Identifier Type: -

Identifier Source: org_study_id