ImmuniCell® in Patients With Advanced Cancers

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE2

Total Enrollment

8 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-12-31

Study Completion Date

2018-11-27

Brief Summary

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To determine the safety, tolerability, maximum tolerated dose (MTD) and efficacy of ImmuniCell® in patients with melanoma, renal cell cancer (RCC) or non-small cell lung cancer (NSCLC). The study is an adaptive design that has 3 stages: Stage 1 - dose escalation, Stage 2 - efficacy, and Stage 3 - confirm efficacy in one of the tumor types.

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Detailed Description

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This is an open-label trial of ImmuniCell® treatment of patients with malignant melanoma, renal cell cancer (RCC) or non-small cell lung cancer (NSCLC) which are refractory to current treatment or who have indolent disease for which immunotherapy may be beneficial. The trial is designed to identify a safe dose of ImmuniCell® for future clinical trials, to identify a response signal from one or more of the cancers under investigation and to confirm the safety and efficacy in the selected target tumour.

The trial has three stages:

Stage I comprising a safety cohort of patients to identify a safe dose Stage II comprising an expanded patient group for response signal identification Stage III to confirm efficacy and safety.

Conditions

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Malignant Melanoma Non-small Cell Lung Cancer Renal Cell Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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ImmuniCell®

Subjects will receive 6 cycles of ImmuniCell®, one infusion over an hour, at two-week intervals. During Stage 1, intra-patient dose escalation to achieve a total dose of 30 x 109 γδ T cells.

Group Type EXPERIMENTAL

ImmuniCell®

Intervention Type BIOLOGICAL

Autologous γδ T Lymphocytes

Interventions

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ImmuniCell®

Autologous γδ T Lymphocytes

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

1. Male or female patients aged ≥18 years
2. Performance status Eastern Cooperative Oncology Group (ECOG) 0 or 1
3. Subjects with histological or cytological confirmation of advanced malignant melanoma, renal cell carcinoma or NSCLC which are refractory to current standard treatments or who have indolent disease for which immunotherapy may be beneficial
4. Measurable disease according to the irRC criteria
5. Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted \<2 weeks prior to Cycle 1:

* Creatinine ≤ 1.5 x upper limit of normal (ULN) OR a calculated creatinine clearance ≥ 50 ml/min
* Total bilirubin ≤ 1.5 x ULN
* Alanine transaminase (ALT) and aspartate transaminase (AST) ≤ 2.5 x ULN or ≤ 5 x ULN with liver metastases
* Absolute lymphocyte count ≥1.0 x 10E9/L
* Absolute Neutrophil Count (ANC) ≥1.5 x 10E9/L
* Platelets ≥100 x 10E9/L
* Haemoglobin ≥ 10 g/dL
6. Life expectancy of at least 3 months
7. Suitable increase in starting γδ T cell number to final γδ T cell number in the proliferation assay between 10 days in culture
8. Able to give informed, written consent
9. For female patients and female partners of male patients: must be surgically sterile, postmenopausal, or compliant with two forms of contraception (one of which must be a barrier method) during and for 6 months after the treatment period; female patients must have a negative urine pregnancy test at screening and must not be breast-feeding.

Exclusion Criteria

1. Other primary cancers apart from non-melanoma skin cancers, carcinoma - in situ of the cervix, or a prior cancer treated with curative intent more than 2 years ago without any evidence or recurrent disease
2. Uncontrolled systemic infection
3. Systemic steroid therapy or other immune-suppressants (except in cases where the patient is receiving treatment with replacement doses for adrenal insufficiency)
4. Treatment with bisphosphonates, for instance zoledronate, in the previous 3 months and throughout the trial
5. New York Heart Association (NYHA) functional class ≥3 or myocardial infarction within 6 months
6. Clinically-significant uncontrolled cardiac arrhythmia other than asymptomatic atrial fibrillation not requiring therapy.
7. Ulcerative Colitis / Inflammatory bowel disease, Addison's disease
8. Pregnancy or lactation before or during the trial. A urine pregnancy test will be carried out at screening
9. Taking any other investigational medicinal product (IMP) or participation in another interventional clinical trial in the previous 30 days
10. Less than 4 weeks since systemic anti-cancer therapy (tyrosine kinase inhibitors, chemotherapy, immunotherapy, hormonal therapy, radiotherapy) and less than 6 weeks since mitomycin C and nitrosureas
11. Substance abuse, medical, psychological or social conditions that may interfere with the subject's participation in the trial or evaluation of the trial results
12. Any other condition considered by a trial physician to be inappropriate for inclusion to the study such as contraindications to leukapheresis (contraindications to heparin which are: recent cerebral haemorrhage; peptic ulcer; recent surgery to eye or nervous system; hypersensitivity to heparin; past history of Type II heparin induced thrombocytopenia; past history of significant spontaneous haemorrhage; known haemophilia or other bleeding disorder).
13. Serological evidence of active infection

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No