A Phase I Study to Investigate Tolerability and Efficacy of Autologous Lymphoid Effector Cells Specific Against Tumour-cells (ALECSAT) Administered to Patients With Glioblastoma Multiforme (GBM)
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Glioblastoma Multiforme
- Sponsor
- CytoVac A/S
- Enrollment
- 23
- Locations
- 1
- Primary Endpoint
- Observation of tolerability and sideeffects of treatment monitored by objective medical examinations, Karnofsky score and QOL interviews.
- Status
- Completed
- Last Updated
- 9 years ago
Overview
Brief Summary
It is the primary objective of this study to show safety and tolerability for administration of the cell based immunotherapy ALECSAT to patients with Glioblastoma brain cancer. It is a secondary objective to establish if any indications of positive therapeutic or palliative effects may be observed.
Detailed Description
The primary objective for this study is to establish if any side effects or toxicity issues occur, that will prevent further clinical development of the autologous cell based immunotherapy ALECSAT in Glioblastoma (GBM) or to establish if there are side effects or toxicity issues, that will suggest that the further clinical development planned, has to change course significantly. It is a primary objective to show safety and tolerability for administration of ALECSAT, thus not meeting this endpoint, may stop further clinical development of ALECSAT. The secondary objective for this study is to establish if any indications of a positive therapeutic or palliative effect may be observed. As this is a secondary objective, no observed significant positive clinical effect, will not prevent further clinical development or in itself, trigger changes in the further clinical development planned. The overall endpoint of the study is to develop a new therapeutic approach that may slow down or stop disease progression in late stage GBM patients. ALECSAT is an autologous cell based immunotherapy based on the patient's own Natural Killer cells and CytoToxic T cells. The cells are isolated from the patient's own blood - activated and expanded in number before re administering i. v.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Recurrence of GBM tumour documented by MRI and PET in patients having received all available standard treatment.
- •Be over the age of 18 and capable of understanding the information and giving informed consent.
- •Adequate performance status \> 50% (see below\*).
- •Performance is monitored according to the Karnofsky Performance Score (KPS)
- •100% - normal, no complaints, no signs of disease
- •90% - capable of normal activity, few symptoms or signs of disease
- •80% - normal activity with some difficulty, some symptoms or signs
- •70% - caring for self, not capable of normal activity or work
- •60% - requiring some help, can take care of most personal requirements
- •50% - requires help often, requires frequent medical care
Exclusion Criteria
- •A low blood count (haemoglobin \< 6.0 mmol/l).
- •Lymphocyte counts below 0.8 x 109/l.
- •Positive tests for anti-HIV-1/2;
- •Positive tests for HBsAg,
- •Positive tests for anti-HBc and Anti-HCV.
- •Syphilis i.e. being positive in a Treponema Pallidum test.
- •Uncontrolled serious bacterial, viral, fungal or parasitic infection.
- •Clinically significant autoimmune disorders or conditions of immune suppression.
- •Treatment with chemotherapy three weeks prior to inclusion in the clinical trial.
- •Pregnant women cannot be included in the trial. Fertile women can only be included with a negative pregnancy test and must use contraceptives during the study.
Outcomes
Primary Outcomes
Observation of tolerability and sideeffects of treatment monitored by objective medical examinations, Karnofsky score and QOL interviews.
Time Frame: 3 months
Secondary Outcomes
- Potential clinical effect will be monitored by PET-MRI and SPECT scanning of the brain.(3 months)