A Phase I Study to Investigate Tolerability and Efficacy of ALECSAT Administered to Glioblastoma Multiforme Patients

NCT ID: NCT01588769

Last Updated: 2016-06-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-08-31
• Study Completion Date: 2013-04-30

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.

Conditions

Glioblastoma Multiforme

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

One arm

3 doses of ALECSAT cell based immunotherapy planned for all enrolled patients

Group Type: EXPERIMENTAL

ALECSAT cell based immunotherapy

Intervention Type: BIOLOGICAL

I.V. injected Cell Based Medicinal Product, containing between 10 million and one billion autologous Cytotoxic T cells and Natural Killer cells.

Interventions

ALECSAT cell based immunotherapy

I.V. injected Cell Based Medicinal Product, containing between 10 million and one billion autologous Cytotoxic T cells and Natural Killer cells.

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

1. Recurrence of GBM tumour documented by MRI and PET in patients having received all available standard treatment.

2. Be over the age of 18 and capable of understanding the information and giving informed consent.

3. 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
• 40% - disabled, requires special care and help
• 30% - severely disabled, hospital admission indicated but no risk of death
• 20% - very ill, urgently requiring admission, requires supportive measures or treatment
• 10% - moribund, rapidly progressive fatal disease processes
• 0% - death.

Exclusion Criteria

1. A low blood count (haemoglobin < 6.0 mmol/l).

2. Lymphocyte counts below 0.8 x 109/l.

3. Positive tests for anti-HIV-1/2;

4. Positive tests for HBsAg,

5. Positive tests for anti-HBc and Anti-HCV.

6. Syphilis i.e. being positive in a Treponema Pallidum test.

7. Uncontrolled serious bacterial, viral, fungal or parasitic infection.

8. Clinically significant autoimmune disorders or conditions of immune suppression.

9. Treatment with chemotherapy three weeks prior to inclusion in the clinical trial.

10. 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.

11. Blood transfusions within 48 hours prior to donation of blood for ALECSAT production.

12. Inclusion in other clinical trials 6 weeks prior to inclusion in the trial.

13. The patient's medical condition is evaluated to be so poor that there is a significant risk for the patient to be part of the trial and to evaluate any effects of the treatment.

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

Sponsors

CytoVac A/S

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Martin R Jensen, PhD

Role: STUDY_DIRECTOR

CytoVac A/S (Sponsor)

Locations

Department of Neurosurgery, Rigshospitalet

Copenhagen, , Denmark

Countries

Denmark

Other Identifiers

2011-002180-22

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CV003

Identifier Type: -

Identifier Source: org_study_id