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Trial · NCT06764680

Oral Chemotherapy, Targeted Therapy and Immunotherapy With/Without Radiotherapy as 3rd- or Later-line Therapy for Advanced MSS/pMMR Colorectal Cancer

NCT06764680, Phase 2, Recruiting, Sun Yat-sen University

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Oral Chemotherapy, Targeted Therapy and Immunotherapy With/Without Radiotherapy as 3rd- or Later-line Therapy for Advanced MSS/pMMR Colorectal Cancer. Trials, record NCT06764680. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06764680

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Trial

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

Title
Oral Chemotherapy, Targeted Therapy and Immunotherapy With/Without Radiotherapy as 3rd- or Later-line Therapy for Advanced MSS/pMMR Colorectal Cancer
NCT number
NCT06764680
Status
Recruiting
Phases
Phase 2
Enrollment
57 participants, estimated
Lead sponsor
Sun Yat-sen University
Conditions
Colorectal Cancer Metastatic, Chemotherapy, Targeted Therapy, Immunotherapy, Radiotherapy, Intensity-Modulated
Interventions
Trifluorouracil tepidopyrimidine, Bevacizumab, Sindilizumab, IMRT
First posted
2025-01-08
Last updated
2025-08-24

Source ClinicalTrials.gov

Registered outcomes5

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

ListOutcomeTime frameDescription
PrimaryObjective response rate (ORR)Baseline, 6-8 weeks after treatment completeObjective response rate (ORR) was defined as the percentage of CR+PR among the patients who could be evaluated for efficacy.
SecondaryDisease control rate (DCR)Baseline, 6-8 weeks after treatment completeDisease control rate (DCR) was defined as the percentage of CR+PR+SD among the patients who could be evaluated for efficacy.
SecondaryProgression-free survival (PFS)month 6, year 1, year 2Progression-free survival (PFS) was calculated from the date of treatment to either the date of disease progression, death or last follow-up.
SecondaryOverall survival (OS)month 6, year 1, year 2Overall survival (OS) was calculated from the date of treatment to either the date of death or last follow-up.
SecondaryTreatment related toxicityBaseline, 6-8 weeks after treatment completeGrading of acute toxicity would be assessed according to National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0.

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.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT06764680

GET https://conductscience.org/api/trials/v1/NCT06764680/registered