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Trial · NCT07902258

An Exploratory Study of Single-Dose Neoadjuvant Nivolumab Without Surgical Delay in Patients With Resectable HCC

NCT07902258, Phase 2, Not yet recruiting, National Taiwan University Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. An Exploratory Study of Single-Dose Neoadjuvant Nivolumab Without Surgical Delay in Patients With Resectable HCC. Trials, record NCT07902258. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07902258

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Trial

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

Title
An Exploratory Study of Single-Dose Neoadjuvant Nivolumab Without Surgical Delay in Patients With Resectable HCC
NCT number
NCT07902258
Status
Not yet recruiting
Phases
Phase 2
Enrollment
40 participants, estimated
Lead sponsor
National Taiwan University Hospital
Conditions
Hepato Cellular Carcinoma (HCC), Immune Checkpoint Inhibitor, Neoadjuvant Therapy
Interventions
Nivolumab
First posted
2026-10-28
Last updated
2026-10-28

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryFeasibility of single-dose neoadjuvant Nivolumab for resectable HCCapproximately within 8 weeks after enrollmentFeasibility is evaluated by whether curative-intent surgery could be performed without delay exceeding \>14 days from the planned date.
Primary56-week event-free survival56 weeks from the date of neoadjuvant Nivolumab intravenous infusion
Prespecified events including: delay of curative-intent surgery by exceeding \>14 days attributable to neoadjuvant nivolumab, surgical cancellation due to any treatment-related adverse events or clinical disease progression, postoperative disease recurrence, or death from any cause.
SecondaryTo assess the safety and pathological response of single-dose neoadjuvant Nivolumab for resectable HCC56 weeks from the date of neoadjuvant Nivolumab intravenous infusionAdverse events, pathological response

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/NCT07902258

GET https://conductscience.org/api/trials/v1/NCT07902258/registered