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CompletedNCT00379470Updated May 1, 2012

Effect of NovoTTF-100A in Recurrent Glioblastoma Multiforme (GBM)

A Phase 3 interventional study of NovoTTF-100A in Recurrent Glioblastoma Multiforme, sponsored by NovoCure Ltd.. Completed at 25 sites in 7 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-05-01.

Sponsored by NovoCure Ltd. · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
236
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The study is a randomized, controlled trial, designed to test the efficacy and safety of a new medical device, the NovoTTF-100A. The device is an experimental, portable, battery operated device for chronic treatment of patients with recurrent or progressive glioblastoma multiforme (GBM) using alternating electric fields (termed TTFields).

Read the detailed description

PAST CLINICAL EXPERIENCE:

The effect of the electric fields generated by the NovoTTF-100A device (TTFields) has been tested in two pilot trials in humans. The data from these trials suggest NovoTTF-100A may improve time to disease progression and overall survival of recurrent GBM patients. Although the number of patients in the pilot trials is small, The FDA has determined that the data gathered so far warrant testing of NovoTTF-100A treatment as a possible therapy for patients with recurrent GBM.

DESCRIPTION OF THE TRIAL:

Patients with GBM whose disease has recurred or progressed despite standard treatment (Surgery, radiation therapy, Temozolomide treatment) and meet all of the requirements for participation in the study will be randomly assigned to one of two groups:

  1. Treatment with the NovoTTF-100A device, or
  2. Treatment with the best standard of care practiced at each of the participating centers.

If assigned to the best standard of care group, patients will receive a chemotherapeutic agent chosen based on their prior treatments and the standard of care practiced at each treating center.

If assigned to the NovoTTF-100A group, the patients will be treated continuously for as long as their disease is stable or regressing. NovoTTF-100A treatment will consist of wearing four electrically insulated electrodes on the head. Electrode placement will require shaving of the scalp before treatment. After an initial short hospitalization (24 hours) patients will be released to continue treatment at home where they can maintain their regular daily routine.

During the trial, regardless of whether assigned to the NovoTTF-100A treatment group or the best standard of care group, patients will need to return once every month the hospital outpatient clinics where they will be examined by a physician and undergo routine laboratory examinations. These routine visits will continue for as long as the patient's disease is not progressing. After progression, if such occurs, patients will need to return once per month for two more months to the outpatient clinic for similar follow up examinations.

During the visits to the clinic patients will be examined physically and neurologically. Additionally, routine blood tests and ECG will be performed. A routine MRI of the head will be performed at baseline and after 2, 4 and 6 months. After this follow up plan, patients will be contacted once per month by telephone to answer basic questions about their health status.

SCIENTIFIC BACKGROUND:

Electric fields exert forces on electric charges similar to the way a magnet exerts forces on metallic particles within a magnetic field. These forces cause movement and rotation of electrically charged biological building blocks, much like the alignment of metallic particles seen along the lines of force radiating outwards from a magnet.

Electric fields can also cause muscles to twitch and if strong enough may heat tissues. TTFields are alternating electric fields of low intensity. This means that they change their direction repetitively many times a second. Since they change direction very rapidly (200 thousand times a second), they do not cause muscles to twitch, nor do they have any effects on other electrically activated tissues in the body (brain, nerves and heart). Since the intensities of TTFields in the body are very low, they do not cause heating.

The breakthrough finding made by NovoCure was that finely tuned alternating fields of very low intensity, now termed TTFields (Tumor Treating Fields), cause a significant slowing in the growth of cancer cells. Due to the unique geometric shape of cancer cells when they are multiplying, TTFields cause the building blocks of these cells to move and pile up in such a way that the cells physically explode. In addition, cancer cells also contain miniature building blocks which act as tiny motors in moving essential parts of the cells from place to place. TTFields cause these tiny motors to fall apart since they have a special type of electric charge.

As a result of these two effects, cancer tumor growth is slowed and can even reverse after continuous exposure to TTFields.

Other cells in the body (normal healthy tissues) are affected much less than cancer cells since they multiply at a much slower rate if at all. In addition TTFields can be directed to a certain part of the body, leaving sensitive areas out of their reach.

In conclusion, TTField hold the promise of serving as a brand new cancer treatment with very few side effects and promising affectivity in slowing or reversing this disease.

02

Conditions studied

  • Recurrent Glioblastoma Multiforme

Keywords

  • Brain tumor
  • Treatment
  • Minimal toxicity
  • GBM
  • Glioblastoma
  • Recurrent
  • TTFields
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In context

Glioblastoma

1,920 studies on the registry are indexed under Glioblastoma; 450 are open to participants now.

This study's enrollment of 236 is above the median of 36 across 1,618 interventional studies indexed under Glioblastoma.

Browse Glioblastoma studies →

Lead sponsor

NovoCure Ltd. is the lead sponsor of 19 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Pathological evidence of GBM using WHO classification criteria.
  • > 18 years of age.
  • Not a candidate for further radiotherapy or additional resection of residual tumor.
  • Patients with disease progression (by Macdonald criteria i.e., > 25% or new lesion) documented by CT or MRI within 4 weeks prior to enrollment
  • Karnofsky scale ≥ 70
  • Life expectancy at least 3 months
  • Participants of childbearing age must use effective contraception.
  • All patients must sign written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Actively participating in another clinical treatment trial
  • Within 4 weeks from surgery for recurrence
  • Within 4 weeks from any prior chemotherapy.
  • Within 4 weeks from radiation therapy
  • Pregnant
  • Significant co-morbidities (within 4 weeks prior to enrollment):

    1. Significant liver function impairment - AST or ALT > 3 times the upper limit of normal
    2. Total bilirubin > upper limit of normal
    3. Significant renal impairment (serum creatinine > 1.7 mg/dL)
    4. Coagulopathy (as evidenced by PT or APTT >1.5 times control in patients not undergoing anticoagulation)
    5. Thrombocytopenia (platelet count \< 100 x 103/μL)
    6. Neutropenia (absolute neutrophil count \< 1 x 103/μL)
    7. Anemia (Hb \< 10 g/L)
    8. Severe acute infection
  • Implanted pacemaker, defibrillator or deep brain stimulator, or documented clinically significant arrhythmias.
  • Infra-tentorial tumor
  • Evidence of increased intracranial pressure (midline shift > 5mm, clinically significant papilledema, vomiting and nausea or reduced level of consciousness)
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Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
236 participants (actual)

Study arms

  • Active comparator
    Best Standard of Care

    Patients randomized to the BSC group will be treated with one chemotherapy according to the BSC practiced at each center.

    Device: NovoTTF-100A

  • Experimental
    NovoTTF-100A

    Device: NovoTTF-100A

Interventions

  • DeviceNovoTTF-100A

    multiple four-week courses of continuous NovoTTF-100A treatment

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What researchers measure

Primary outcomes

  1. Overall Survival

    Time frame: 2 years from initiation of accrual

Secondary outcomes

  1. Progression free survival at 6 months (PFS6)

    Time frame: 2 years from initiation of accrual

  2. Median Time to Disease Progression (TTP)

    Time frame: 2 years from initiation of accrual

  3. % 1-year survival

    Time frame: 2 years from initiation of accrual

  4. Radiological response (Macdonald criteria)

    Time frame: 2 years from initiation of accrual

  5. Quality of life assessment (EORTC QLQ-C30)

    Time frame: 2 years from initiation of accrual

  6. Adverse events severity and frequency

    Time frame: 2 years from initiation of accrual

07

Study locations

25 sites
  • Northwestern University
    Chicago, Illinois 60611, United States
  • University of Illinois in Chicago
    Chicago, Illinois 60612, United States
  • Evanston Northwestern Healthcare
    Evanston, Illinois 60201, United States
  • Boston University Medical Center
    Boston, Massachusetts 02118, United States
  • Beth Israel Deaconess Medical Center
    Boston, Massachusetts 02215, United States
  • Lahey Clinic Medical Center
    Burlington, Massachusetts 01850, United States
  • NJ Neuroscience Institute - JFK Medical Center
    Edison, New Jersey 08818, United States
  • Memorial Sloan Kettering Cancer Center
    New York, New York 10021, United States
  • Weill Cornell Medical College
    New York, New York 10021, United States
  • Columbia University Medical Center
    New York, New York 10032, United States
  • University Hospitals of Cleveland
    Cleveland, Ohio 44106, United States
  • Cleveland Clinic
    Cleveland, Ohio, United States
  • University of Pittsburgh Medical Center (UPMC)
    Pittsburgh, Pennsylvania 15232, United States
  • University of Virginia
    Charlottesville, Virginia, United States
  • Medical College of Wisconsin
    Milwaukee, Wisconsin 53226, United States
  • University Hospital Graz
    Graz, Austria
  • FN Brno - Masaryk University
    Brno, Czech Republic
  • Na Homolce Hospital
    Prague, Czech Republic
  • Hospital of Neurology Lyon - University Claude Bernard Lyon 1
    Lyon, France
  • Group Hospitals Pitie-Salpetriere
    Paris, France
  • University Hospital Augsburg
    Augsburg, Germany
  • University Medical Center Hamburg-Eppendorf
    Hamburg, Germany
  • University Hospital of Schleswig-Holstein
    Kiel, 24105, Germany
  • Tel Aviv Sourasky Medical Center
    Tel Aviv, 64239, Israel
  • Centre Hospitalier Universitaire Vaudois
    Lausanne, Switzerland
08

References and documents

Publications

  • Kirson ED, Gurvich Z, Schneiderman R, Dekel E, Itzhaki A, Wasserman Y, Schatzberger R, Palti Y. Disruption of cancer cell replication by alternating electric fields. Cancer Res. 2004 May 1;64(9):3288-95. doi: 10.1158/0008-5472.can-04-0083. PubMed 15126372 ↗
  • Kirson ED, Dbaly V, Tovarys F, Vymazal J, Soustiel JF, Itzhaki A, Mordechovich D, Steinberg-Shapira S, Gurvich Z, Schneiderman R, Wasserman Y, Salzberg M, Ryffel B, Goldsher D, Dekel E, Palti Y. Alternating electric fields arrest cell proliferation in animal tumor models and human brain tumors. Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):10152-7. doi: 10.1073/pnas.0702916104. Epub 2007 Jun 5. PubMed 17551011 ↗
  • Salzberg M, Kirson E, Palti Y, Rochlitz C. A pilot study with very low-intensity, intermediate-frequency electric fields in patients with locally advanced and/or metastatic solid tumors. Onkologie. 2008 Jul;31(7):362-5. doi: 10.1159/000137713. Epub 2008 Jun 24. PubMed 18596382 ↗
  • Stupp R, Wong ET, Kanner AA, Steinberg D, Engelhard H, Heidecke V, Kirson ED, Taillibert S, Liebermann F, Dbaly V, Ram Z, Villano JL, Rainov N, Weinberg U, Schiff D, Kunschner L, Raizer J, Honnorat J, Sloan A, Malkin M, Landolfi JC, Payer F, Mehdorn M, Weil RJ, Pannullo SC, Westphal M, Smrcka M, Chin L, Kostron H, Hofer S, Bruce J, Cosgrove R, Paleologous N, Palti Y, Gutin PH. NovoTTF-100A versus physician's choice chemotherapy in recurrent glioblastoma: a randomised phase III trial of a novel treatment modality. Eur J Cancer. 2012 Sep;48(14):2192-202. doi: 10.1016/j.ejca.2012.04.011. Epub 2012 May 18. PubMed 22608262 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 1, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00379470
Lead sponsor
NovoCure Ltd.
Responsible party
Sponsor
First posted
Sep 21, 2006
Start date
Sep 2006
Primary completion
Nov 2009
Completion
Jan 2011
Last update
May 1, 2012

Study contacts

Phillip Gutin, MD
principal investigator · Memorial Sloan Kettering Cancer Center
Roger Stupp, MD
principal investigator · University of Lausanne Hospital - Multidisciplinary Oncology Center

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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