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NCT06020885Active, not recruitingPhase 1

Fraction Dose Escalation of Split-course Hypofractionated Concurrent Chemoradiotherapy Following Induction Chemo-immunotherapy in Unresectable Locally Advanced Esophageal Squamous Carcinoma: a Phase I Study.

Source: ClinicalTrials.gov · Last updated 21 Jul 2025

Brief summary (registry, in English)

This Phase I study is to determine the maximum tolerated fraction dose (MTD) for split-course hypo-CCRT following induction chemo-immunotherapy in LA-ESCC patients, to clarify the dosimetric advantage of split-course hypo-CCRT, and to investigate the treatment-related toxicities and quality of life of the new regimen.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
18 (estimated)
First submitted
26 Aug 2023
Start date
31 Aug 2023
Primary completion date
30 Oct 2025
Lead sponsor
Sun Yat-sen University
NCT number
NCT06020885

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 18
  • From 31 Aug 2023 to the primary completion date, 30 Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • contraindication for radiotherapy or chemotherapy

Other illness

  • prior malignancies, except for curable non-melanoma skin cancer or cervical carcinoma in situ

Other

  • distant metastasis, except for celiac or supraclavicular lymph nodes metastases

Who the study is looking for

  • histologically confirmed ESCC
  • II-IVB stages (IVB stage only with metastatic celiac or supraclavicular lymph nodes) based on the TNM staging system proposed by the International Union Against Cancer (UICC 2002)
  • Eastern Cooperative Oncology Group (ECOG) performance status score 0-1
  • Charlson Comorbidity Index score≤4
  • oral medication can be administered despite esophageal obstruction
  • adequate hematological, renal and hepatic functions

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sun Yat-sen University Cancer Center
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.