Mode
Text Size
Log in / Sign up
Phase 2 N=124 Randomized Triple-blind Treatment

A Study of ICT-107 Immunotherapy in Glioblastoma Multiforme (GBM)

Glioblastoma Multiforme

Enrolled (actual)
124
Serious AEs
12.2%
Results posted
Oct 2014
Primary outcome: Primary: Overall Survival (OS) — 18.3; 16.7 months of survival

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
ICT-107 (Biological); Placebo DC (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Precision Life Sciences Group
Primary completion
Dec 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Survival (OS)
18.3; 16.7
PRIMARY
Overall Survival in HLA-A2 Patients
18.3; 12.9
SECONDARY
PFS
11.2; 9.0 0.010 sig
SECONDARY
Progression Free Survival in HLA- A2 Patients
11.2; 7.2 0.033 sig

Summary

This is a phase 2, multicenter study to determine the safety and efficacy of ICT-107 in treating a type of brain tumor called Glioblastoma Multiforme (GBM). ICT-107 is an immunotherapy in which the patient's immune response will be stimulated to kill the tumor cells. Patients must be newly diagnosed with GBM and not yet received chemoradiation. Some of the patient's white blood cells (WBC) will be removed and cultured in a laboratory with purified antigens, similar to those on GBM cells. The patient's own WBC/DC that have been exposed to the tumor antigens will then be given back to the patient as a vaccine over several months. The goal is for the ICT-107 vaccine to stimulate the patient's immune response to kill the remaining GBM tumor cells after surgery and chemotherapy.

Eligibility Criteria

Inclusion Criteria

  • Confirmed, initial diagnosis of GBM. Patients must be newly diagnosed with GBM and not yet received chemoradiation.
  • ≥ 18 years of age
  • HLA-A1 or HLA-A2 positive
  • KPS score of ≥ 70%
  • Baseline hematologic studies and chemistry profiles must meet the following criteria:

Hemoglobin (Hgb) > 9.9 g/dL total granulocyte count > than 1000/mm3 platelet count > 100,000/mm3 blood urea nitrogen (BUN) < 30 mg/dL creatinine < 2 mg/dL alkaline phosphatase (ALP), aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 4x upper limit of normal (ULN) prothrombin time (PT) and activated partial thromboplastin time (PTT) ≤ 1.6x control unless therapeutically warranted

  • Female patients of child-bearing potential must have negative serum pregnancy test
  • If not surgically sterile, male and female patients of childbearing age must use double barrier contraception (hormonal; intrauterine device; barrier)
  • Sufficient paraffin embedded tumor sample for analysis MGMT methylation status
  • Written informed consent, Release of Medical Records Form and Health Insurance Portability and Accountability Act (HIPAA) reviewed and signed by patient or legally authorized representatives

Exclusion Criteria

  • Recurrent disease
  • Radiosurgery including Gamma Knife, linear accelerator based radiosurgery, CyberKnife and placement of Gliadel wafer
  • Presence of any other active malignancy or prior history of malignancy (except for basal cell carcinoma of the skin)
  • Severe pulmonary, cardiac or other systemic disease
  • Congestive heart failure Class III or IV according to New York Heart Association (NYHA)
  • Presence of an acute infection requiring active treatment with antibiotics/antivirals; prophylactic administration is allowed
  • Known history of an autoimmune disorder
  • Known human immunodeficiency virus (HIV) positivity or acquired immunodeficiency syndrome (AIDS) related illness or other serious medical illness
  • Breastfeeding
  • Received any other therapeutic investigational agent within 30 days of enrollment
  • Reduction of steroids (dexamethasone) to a maximum of 2 mg twice a day (BID) prior to the first administration of study vaccine
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01280552). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search