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Trial · NCT06801730

Irinotecan Liposomes Combined With Bevacizumab in the Treatment of Recurrent Glioma

NCT06801730, Phase 2, Recruiting, Zhifeng Tian,MD

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Irinotecan Liposomes Combined With Bevacizumab in the Treatment of Recurrent Glioma. Trials, record NCT06801730. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06801730

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Trial

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

Title
Irinotecan Liposomes Combined With Bevacizumab in the Treatment of Recurrent Glioma
NCT number
NCT06801730
Status
Recruiting
Phases
Phase 2
Enrollment
38 participants, estimated
Lead sponsor
Zhifeng Tian,MD
Conditions
Glioma
Interventions
Irinotecan liposome combined with bevacizumab
First posted
2025-01-30
Last updated
2025-01-30

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryObjective response rateFrom date of randomization until the date of one yearThe proportion of patients with optimal tumor response, complete response (CR) or partial response (PR) assessed based on the RECIST v1.1 criteria
SecondaryProgression free survivalFrom date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 monthsThe time from the start of treatment to the first recording of PD or death, whichever occurs first
SecondaryOverall survivalFrom date of randomization until the date of death from any cause, assessed up to 24 monthsThe time between the start of treatment and the first recorded death

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/NCT06801730

GET https://conductscience.org/api/trials/v1/NCT06801730/registered