CAR-pNK Cell Immunotherapy in MUC1 Positive Relapsed or Refractory Solid Tumor

Sponsor

PersonGen BioTherapeutics (Suzhou) Co., Ltd. (Industry)

Overall Status

Unknown status

CT.gov ID

NCT02839954

Collaborator

The First People's Hospital of Hefei (Other), Hefei Binhu Hospital (Other)

Enrollment

Location

Arm

Duration (Months)

0.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the safety and effectiveness of CAR-pNK cell immunotherapy in patients with MUC1 positive relapsed or refractory solid tumor.

Condition or Disease	Intervention/Treatment	Phase
Hepatocellular Carcinoma Non-small Cell Lung Cancer Pancreatic Carcinoma Triple-Negative Invasive Breast Carcinoma Malignant Glioma of Brain Colorectal Carcinoma Gastric Carcinoma	Biological: anti-MUC1 CAR-pNK cells	Phase 1/Phase 2

Study Design

Study Type:

Interventional

Anticipated Enrollment :

10 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Study Evaluating the Efficacy and Safety of Chimeric Antigen Receptor-Modified pNK Cells in MUC1 Positive Advanced Refractory or Relapsed Solid Tumor

Study Start Date :

Jul 1, 2016

Anticipated Primary Completion Date :

Jul 1, 2017

Anticipated Study Completion Date :

Jul 1, 2018

Arms and Interventions

Arm	Intervention/Treatment
Experimental: CAR-pNK Cell immunotherapy Enrolled patients will receive CAR-pNK cell immunotherapy with a novel specific chimeric antigen receptor targeting MUC1 antigen by infusion.	Biological: anti-MUC1 CAR-pNK cells Other Names: Chimeric antigen receptor NK cells with specificity for MUC1

Arm

Intervention/Treatment

Experimental: CAR-pNK Cell immunotherapy

Enrolled patients will receive CAR-pNK cell immunotherapy with a novel specific chimeric antigen receptor targeting MUC1 antigen by infusion.

Biological: anti-MUC1 CAR-pNK cells

Other Names:

Chimeric antigen receptor NK cells with specificity for MUC1

Outcome Measures

Primary Outcome Measures

Phase I: Adverse events attributed to the administration of the anti-MUC1 CAR-pNK cells [2 years]
Determine the toxicity profile of the MUC1 targeted CAR-pNK cells with Common Toxicity Criteria for Adverse Effects (CTCAE) version 4.0.

Secondary Outcome Measures

Phase II: Objective Response Rate [2 years]
The objective response rate (ORR) is defined as the proportion of patients who achieve radiographic partial or complete response (PR or CR) according to the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 guideline.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male and female subjects with MUC1+ malignancies in patients with no available curative treatment options who have limited prognosis (several months to < 2 year survival) with currently available therapies will be enrolled:

Eligible diseases: MUC1+ malignant glioma of brain, colorectal carcinoma, gastric carcinoma, hepatocellular carcinoma, non-small cell lung cancer, pancreatic carcinoma and triple-negative basal-like breast carcinoma.
Patients 18 years of age or older, and must have a life expectancy > 12 weeks.
MUC1 is expressed in malignancy tissues by immuno-histochemical (IHC).
Eastern cooperative oncology group (ECOG) performance status of 0-2 or karnofsky performance status (KPS) score is higher than 60.
Presence of measurable disease by RECIST.
Females of child-bearing potential must have a negative pregnancy test and all subjects must agree to use an effective method of contraception for up to two weeks after the last infusion of CAR-pNK cells.
Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements: White blood cell count (WBC) ≥ 2500c/ml, Platelets ≥ 50×10^{9/L, Hb ≥
9.0g/dL, lymphocyte (LY) ≥ 0.7×10}9/L, LY% ≥ 15%, Alb ≥ 2.8g/dL, serum lipase and amylase < 1.5×upper limit of normal, serum creatinine ≤ 2.5mg/dL, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 5×upper limit of normal, serum total bilirubin ≤ 2.0mg/dL. These tests must be conducted within 7 days prior to registration.
Ability to give informed consent.

Exclusion Criteria:

Patients with symptomatic central nervous system (CNS) involvement.
Pregnant or nursing women may not participate.
Active HIV, hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
Serious illness or medical condition which would not permit the patient to be managed according to the protocol, including active uncontrolled infection, major cardiovascular, coagulation disorders, respiratory or immune system, myocardial infarction, cardiac arrhythmias, obstructive/restrictive pulmonary disease, or psychiatric or emotional disorders.
Concurrent use of systemic steroids. Recent or current use of inhaled steroids is not exclusionary.
The existence of unstable or active ulcers or gastrointestinal bleeding.
Patients with a history of organ transplantation or are waiting for organ transplantation.
Patients need anticoagulant therapy (such as warfarin or heparin).
Patients need long-term antiplatelet therapy (aspirin at a dose > 300mg/d; clopidogrel at a dose > 75mg/d).