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Trial · NCT07448480

Comprehensive Analysis of Chemotherapy and Targeted Therapy Outcomes in Recurrent Malignant Gliomas

NCT07448480, Active not recruiting, Blokhin's Russian Cancer Research Center

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Comprehensive Analysis of Chemotherapy and Targeted Therapy Outcomes in Recurrent Malignant Gliomas. Trials, record NCT07448480. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07448480

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Comprehensive Analysis of Chemotherapy and Targeted Therapy Outcomes in Recurrent Malignant Gliomas
NCT number
NCT07448480
Status
Active not recruiting
Enrollment
1,000 participants, actual
Lead sponsor
Blokhin's Russian Cancer Research Center
Conditions
Recurrent Malignant Glioma, Glioblastoma, Anaplastic Astrocytoma, Pleomorphic Xanthoastrocytoma
Interventions
Bevacizumab-Containing Regimens, Non-Bevacizumab Regimens, BRAF ± MEK Targeted Therapy
First posted
2026-03-04
Last updated
2026-03-04

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryOverall Survival (OS)From date of initial brain tumor diagnosis until date of death or last contact with the patient, assessed up to 5 years (censored)Time from the date of initial brain tumor diagnosis to the date of death from any cause or last contact with the patient (censored)
SecondaryProgression-Free Survival 1 (PFS1)From start of chemoradiotherapy until date of first progression or censoring at the start of first-line treatment, assessed up to 5 years
Time from the start of chemoradiotherapy to the date of documented intracranial progression according to RANO 2.0 criteria. Patients who proceeded directly to first-line drug therapy without evidence of progression will be censored at the start of first-line treatment
SecondaryProgression-Free Survival 2 (PFS2)From start of first-line therapy until date of progression or censoring at last instrumental follow-up, assessed up to 5 years
Time from the start of first-line drug therapy to the date of documented intracranial progression according to RANO 2.0 criteria. Patients without documented progression will be censored at the date of last instrumental follow-up (brain MRI or PET-CT with tyrosine/methionine)
SecondaryProgression-Free Survival 3 (PFS3)From start of second-line therapy until date of progression or censoring at last instrumental follow-up, assessed up to 5 years
Time from the start of second-line drug therapy to the date of documented intracranial progression according to RANO 2.0 criteria. Patients without documented progression will be censored at the date of last instrumental follow-up (brain MRI or PET-CT with tyrosine/methionine)
SecondaryProgression-Free Survival 4 (PFS4)From start of third-line therapy until date of progression or censoring at last instrumental follow-up, assessed up to 5 years
Time from the start of third-line drug therapy to the date of documented intracranial progression according to RANO 2.0 criteria. Patients without documented progression will be censored at the date of last instrumental follow-up (brain MRI or PET-CT with tyrosine/methionine)
SecondaryProgression-Free Survival 5 (PFS5)From start of fourth-line therapy until date of progression or censoring at last instrumental follow-up, assessed up to 20 years
Time from the start of fourth-line drug therapy to the date of documented intracranial progression according to RANO 2.0 criteria. Patients without documented progression will be censored at the date of last instrumental follow-up (brain MRI or PET-CT with tyrosine/methionine)

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07448480

GET https://conductscience.org/api/trials/v1/NCT07448480/registered