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Radiodynamic Therapy (RDT) With Gliolan in Patients With First Recurrence of Brain Tumor

Study acronym: ALA-RDTinGBM
StatusRecruiting
PhasePhase 1/2
Started
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Record History

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  1. Notable Primary completion date: Jun 2026 to Jan 2028
    • Study completion date: Jan 2027 to Jan 2028
    v6
  2. Notable Primary completion date: Jul 2024 to Jun 2026
    • Study completion date: Jan 2025 to Jan 2027
    v5
  3. Minor Eligibility criteria shortened, about 6 wordsv4
  4. Minor Re-verified, no change to tracked fieldsv3
  5. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Oct 2022 to Nov 9, 2022
    • Secondary endpoints revised (4)
    • Site details revised
    v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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The investigational drug 5-ALA (known under the trade name Gliolan®) is an approved drug for the surgical removal of malignant glioma (WHO grade III and IV). In this trial, the drug is being tested outside of its actual approval as a radiosensitizer in combination with conventional radiotherapy for first-time recurrence (relapse) of malignant glioma. In this clinical trial, the investigational drug 5-ALA is being used for the first time in a multiple dose escalation regimen in combination with radiotherapy following surgical removal of a recurrent malignant glioma in humans. The investigational drug, 5-ALA, has been used as a single dose to date as a standard of care for visualization of malignant tissue in the surgical removal of gliomas. The planned clinical trial will first and foremost investigate how well repeated administration of the investigational drug 5-ALA is tolerated in combination with radiotherapy. At the same time, the design of the trial serves to optimize this novel therapeutic procedure with regard to the frequency of administration of the investigational drug 5-ALA in combination with radiotherapy for future clinical trials. As a secondary objective, the efficacy of additional 5-ALA administration will also be investigated.
Trial Details
NCT Number NCT05590689
Lead Sponsor Universität Münster
Collaborators: photonamic GmbH & Co. KG
Conditions
(from sponsor)
Glioblastoma
Related terms Glioblastoma
Enrollment 34 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov