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Terminated Phase 3 Interventional Results available

Efficacy and Safety of AP 12009 in Patients With Recurrent or Refractory Anaplastic Astrocytoma or Secondary Glioblastoma

ClinicalTrials.gov ID: NCT00761280

Public ClinicalTrials.gov record NCT00761280. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 19, 2026, 6:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Efficacy and Safety of AP 12009 in Adult Patients With Recurrent or Refractory Anaplastic Astrocytoma or Secondary Glioblastoma as Compared to Standard Chemotherapy Treatment: A Randomized, Actively Controlled, Open Label Clinical Phase III Study.

Study identification

NCT ID
NCT00761280
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Isarna Therapeutics GmbH
Industry
Enrollment
27 participants

Conditions and interventions

Interventions

  • Drug delivery system for administration of AP 12009 Device
  • Placement of Drug Delivery System Procedure
  • carmustine Drug
  • lomustine Drug
  • temozolomide Drug
  • trabedersen Drug

Device · Procedure · Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2008
Primary completion
Jan 31, 2012
Completion
May 31, 2012
Last update posted
Nov 13, 2014

2008 – 2012

United States locations

U.S. sites
3
U.S. states
2
U.S. cities
3
Facility City State ZIP Site status
NJ Neuroscience Institute; JFK Medical Center Edison New Jersey 08820
Winthrop University Hospital Mineola New York 11501
University of Rochester Medical Center Rochester New York 14642

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00761280, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 13, 2014 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00761280 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →