Study of Efficacy and Safety of CRC01 in Adult Large B-cell Lymphoma Patients

Sponsor

Curocell Inc. (Industry)

Overall Status

Recruiting

CT.gov ID

NCT04836507

Collaborator

(none)

Enrollment

Location

Arm

Anticipated Duration (Months)

1.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a multi-center, phase I/II study to determine the efficacy and safety of CRC01 in adult patients with relapsed or refractory large B-cell lymphoma.

Condition or Disease	Intervention/Treatment	Phase
Relapsed Large B-cell Lymphoma Refractory Large B-cell Lymphoma Diffuse Large B-cell Lymphoma (DLBCL) Primary Mediastinal Large B-Cell Lymphoma (PMBCL) High-grade B-cell Lymphoma Transformed Follicular Lymphoma (TFL)	Biological: CRC01 Drug: Fludarabine Drug: Cyclophosphamide	Phase 1/Phase 2

Study Design

Study Type:

Interventional

Anticipated Enrollment :

91 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

An Open-label, Multi-center, Single-arm Phase 1/2 Study to Assess Tolerability, Safety and Efficacy of CRC01 in Adult Patients With Relapsed or Refractory Large B-cell Lymphoma

Actual Study Start Date :

Mar 2, 2021

Anticipated Primary Completion Date :

May 1, 2023

Anticipated Study Completion Date :

Feb 1, 2028

Arms and Interventions

Arm	Intervention/Treatment
Experimental: CRC01 A conditioning chemotherapy regimen of fludarabine and cyclophosphamide will be administered followed by investigational treatment, CRC01.	Biological: CRC01 A single infusion of chimeric antigen receptor (CAR)-transduced autologous T cells administered intravenously at a target dose of 2 x 10^6 anti-CD19 CAR T cells/kg. Drug: Fludarabine Administered according to package insert Drug: Cyclophosphamide Administered according to package insert

Arm

Intervention/Treatment

Experimental: CRC01

A conditioning chemotherapy regimen of fludarabine and cyclophosphamide will be administered followed by investigational treatment, CRC01.

Biological: CRC01

A single infusion of chimeric antigen receptor (CAR)-transduced autologous T cells administered intravenously at a target dose of 2 x 10^6 anti-CD19 CAR T cells/kg.

Drug: Fludarabine

Administered according to package insert

Drug: Cyclophosphamide

Administered according to package insert

Outcome Measures

Primary Outcome Measures

Phase 1 Study: Maximum Tolerated Dose (MTD) which will be the Recommended Phase 2 Dose (RP2D) [28 days]
Phase 2 Pivotal Study: Overall Response Rate (ORR) [5 years]
ORR is defined as the incidence of either a complete response (CR) or a partial response (PR) per the Lugano Criteria for Response Assessment (2014).

Secondary Outcome Measures

Time to response (TTR) [5 years]
Duration of overall response (DOR) [5 years]
Event free survival (EFS) [5 years]
Progression free survival (PFS) [5 years]
Overall survival (OS) [5 years]
Incidence and severity of adverse events (AEs) [5 years]
Incidence of immunogenicity to CRC01 [5 years]
Number of participants with presence of exposure to replication-competent lentivirus (RCL) as Assessed by quantitative polymerase chain reaction (qPCR) [5 years]
Incidence of secondary malignancy [5 years]
Peak concentration (Cmax) of CRC01 transduced cells into target tissues [5 years]
Area under the concentration versus time curve (AUC) of CRC01 transduced cells into target tissues [5 years]
Time to maximum observed concentration (Tmax) of CRC01 transduced cells into target tissues [5 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:

19 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

≥ 19 years of age and provided written informed consent
Histologically confirmed following large B-cell lymphomas according to the World Health Organization classification 2017

Diffuse large B-cell lymphoma, not otherwise specified Including Large cell transformation from follicular lymphoma (Transformed follicular lymphoma)
High-grade B-cell lymphoma, not otherwise specified
High-grade B-cell lymphoma with double-hit/triple-hit
Primary mediastinal large B cell lymphoma

Relapsed or refractory disease after ≥ two lines of chemotherapy including rituximab, anthracycline and either having failed autologous Hematopoietic stem cell transplantation (ASCT) or being ineligible for or not consenting to ASCT.
At least one measurable lesion (Long diameter ≥ 1.5cm)
Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
Adequate renal and hepatic functions based on the laboratory test results

Total Bilirubin ≤ 2.0mg/dL with the exception of patients with Gilbert-Meulengracht syndrome; patients with Gilbert-Meulengracht syndrome may be included if their total bilirubin is ≤ 3 X ULN and direct bilirubin ≤ 1.5 X ULN.
Aspartate transaminase (AST) and Alanine transaminase (ALT) ≤ 3 X Upper Limit of Normal (ULN) for age with exception of liver metastasis; patients with liver metastasis may be included if their AST and ALT are ≤ 5 X ULN.
Serum creatinine ≤ 1.5 X ULN
Estimated Glomerular Filtration Rate (eGFR) ≥ 60mL/min/1.73m2

Adequate hematologic function without transfusions within 2 weeks prior to screening for the study defined as followings:

Hemoglobin > 8.0g/㎗
Absolute Neutrophil Count (ANC) > 1,000/㎕
Absolute Lymphocyte Count (ALC) ≥ 300/㎕
Platelets ≥ 50,000/㎕

Must have a minimum level of pulmonary reserve defined as;

≤ Grade 1 dyspnea per Common terminology criteria for adverse events (CTCAE) v5.0
pulse oxygenation > 91% on room air

Hemodynamically stable, without pericardial effusion and Left Ventricle Ejection Fraction (LVEF) ≥ 50% confirmed by Echocardiogram (ECG) or Multigated Radionuclide Angiography (MUGA)
Must have an apheresis product of non-mobilized cells accepted for manufacturing
Life expectancy ≥ 12 weeks
Women of child-bearing potential and all male participants must agree to use highly effective methods of contraception for at least 12 months following CRC01 infusion and until CRC01 are no longer present by PCR on two consecutive tests

Exclusion Criteria:

Patients with the following medical history

Previous or concurrent malignancy with the following exceptions:
Adequately treated basal cell or squamous cell carcinoma without evidence of recurrence for at least 3 years prior to the study
In situ carcinoma of the cervix or breast, treated curatively and without evidence of recurrence for at least 3 years prior to the study
A primary malignancy which has been completely resected and in complete remission for ≥ 5 years
Unstable angina and/or myocardial infarction within 12 months prior to screening
Thromboembolic events, pulmonary embolism or bleeding diatheses within 6 months prior to screening
Hypoxemia, significant pleural effusion or significant EKG findings within 6 months prior to the screening

Patients with the following concurrent disease at screening:

Central Nervous System (CNS) involvement by malignancy by MRI at screening
Active infection with hepatitis B (HBsAg positive. But, in case of HBcAb IgG positive, the patient can be enrolled in this study if he/she takes prophylactic anti-viral agent.)
Active infection with hepatitis C (HCV RNA positive)
Human immunodeficiency virus (HIV) positive
Active neurological auto-immune or inflammatory disorder (e.g. Guillain Barre Syndrome, Amyotrophic Lateral Sclerosis)
Ventricular tachycardia and atrial fibrillation with rapid ventricular response not controlled with medical treatment within 3 months prior to screening

Rapidly progressing the disease as per investigator's discretion
Had major surgery requiring general anesthesia or mechanical ventilation within 4 weeks prior to screening (For video-assisted thoracoscopic surgery (VATS) or open-and-closed (ONC) surgery can be applied with within 2 weeks prior to screening.)
Severe infection requiring anti-bacterial, anti-fungal or anti-viral medication or uncontrolled active infection
The following treatment history is excluded:

Prior treatment with any prior anti-CD19/anti-CD3 therapy or any other anti-CD19 therapy
Prior treatment with any adoptive T cell therapy
Treatment with any prior gene therapy product
Prior allogeneic HSCT
Patients on oral anticoagulation therapy

Eligible for and consenting to ASCT
Use of investigational medicinal product/device within 4 weeks prior to screening
Pregnant or lactating women
Hypersensitivity reaction to the excipients of CRC01 cell product
The following treatments are excluded:

Anti-neoplastic therapies including chemotherapy, biologic agents, retinoid therapy, radiotherapy, immune therapy, hormonal therapy, etc. other than lymphodepleting chemotherapy within 2 weeks of leukapheresis and within 2 weeks of CRC01 infusion
Steroids: therapeutic doses of steroids must be stopped > 7 days prior to leukapheresis and > 5 days prior to CRC01 infusion. However, the following physiological replacement doses of steroids are allowed: < 6 mg/m2/day hydrocortisone or equivalent
Immunosuppression: any immunosuppressive medication must be stopped > 4 weeks prior to leukapheresis and > 4 weeks prior to CRC01 infusion
Antibody use including anti-CD20 therapy within 4 weeks prior to CRC01 infusion
CNS disease prophylaxis must be stopped > 1 week prior to CRC01 infusion (e.g. intrathecal methotrexate)

Other protocol-related inclusion/exclusion may apply.