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Study of NPC-08 is to Treat for Newly-Diagnosed Malignant Glioma and Recurrent Glioblastoma Multiforme

Primary Purpose

Malignant Glioma

Status
Completed
Phase
Phase 1
Locations
Japan
Study Type
Interventional
Intervention
NPC-08
Sponsored by
Nobelpharma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Glioma focused on measuring NPC-08, carmustine, nitrosourea, safety

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female, aged between 18 and 65 years;
  • Radiographic evidence on cranial MRI of a single contrast-enhancing unilateral supratentorial cerebral tumor;
  • Karnofsky Performance Score of 60 or higher;
  • Willing to practice an effective method of birth control for at least 12 months after wafer implantation surgery;

Exclusion Criteria:

  • More than one focus of tumor or tumor crossing the midline, as assessed by coronal cranial MRI scan;
  • Prior radiotherapy to the brain;
  • Prior chemotherapy for the malignant glioma before the baseline evaluation, or patients who were being treated with chemotherapeutic agents;
  • Known hypersensitivity to nitrosoureas;
  • Participation in any other investigational protocol in the previous 6 months for any type of malignancy;

Sites / Locations

  • The Tazuke Kofukai Foundation Medical Research Kitano Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

NPC-08

Arm Description

Outcomes

Primary Outcome Measures

Overall survival to 12 months

Secondary Outcome Measures

Progression-free survival

Full Information

First Posted
June 10, 2009
Last Updated
October 29, 2013
Sponsor
Nobelpharma
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1. Study Identification

Unique Protocol Identification Number
NCT00919737
Brief Title
Study of NPC-08 is to Treat for Newly-Diagnosed Malignant Glioma and Recurrent Glioblastoma Multiforme
Official Title
A Phase 1/2, Multicenter, Non-Randomized, Open Label Clinical Trial of NPC-08 Implant in Patients Undergoing Surgery for Newly-Diagnosed Malignant Glioma and Recurrent Glioblastoma Multiforme.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
April 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nobelpharma

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate whether NPC-08 is safety and efficacy in the treatment of newly-diagnosed malignant glioma and recurrent glioblastoma multiforme.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Glioma
Keywords
NPC-08, carmustine, nitrosourea, safety

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NPC-08
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
NPC-08
Intervention Description
Polifeprosan 20 with Carmustine 3.85%
Primary Outcome Measure Information:
Title
Overall survival to 12 months
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Progression-free survival
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female, aged between 18 and 65 years; Radiographic evidence on cranial MRI of a single contrast-enhancing unilateral supratentorial cerebral tumor; Karnofsky Performance Score of 60 or higher; Willing to practice an effective method of birth control for at least 12 months after wafer implantation surgery; Exclusion Criteria: More than one focus of tumor or tumor crossing the midline, as assessed by coronal cranial MRI scan; Prior radiotherapy to the brain; Prior chemotherapy for the malignant glioma before the baseline evaluation, or patients who were being treated with chemotherapeutic agents; Known hypersensitivity to nitrosoureas; Participation in any other investigational protocol in the previous 6 months for any type of malignancy;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Masao Mastutani, M.D., D.M.Sci.
Organizational Affiliation
Saitama International Medical Center, Saitama Medical University
Official's Role
Study Director
Facility Information:
Facility Name
The Tazuke Kofukai Foundation Medical Research Kitano Hospital
City
Osaka
Country
Japan

12. IPD Sharing Statement

Learn more about this trial

Study of NPC-08 is to Treat for Newly-Diagnosed Malignant Glioma and Recurrent Glioblastoma Multiforme

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