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NCT06682247Not yet recruiting

A Real-world Study of Chidamide in Combination with PD-1/PD-L1 Antibodies and Anti-angiogenic Agents in Advanced MSS Colorectal Cancer

A Real-world Study of Chidamide in Combination with PD-1/PD-L1 Antibodies and Anti-angiogenic Agents in the Treatment of Microsatellite Stable Advanced Colorectal Cancer

Source: ClinicalTrials.gov · Last updated 12 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is an observational , multicenter, real-world study aimed at evaluating the efficacy and safety of the combination of immune checkpoint inhibitors, chidamide and antiangiogenic agents in Microsatellite Stable advanced colorectal cancer patients.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
7 Nov 2024
Start date
15 Nov 2024
Primary completion date
15 Jun 2025
Lead sponsor
Feng Wang
NCT number
NCT06682247

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 15 Nov 2024 to the primary completion date, 15 Jun 2025
  • No sites listed in no 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.

Other

  • Lack of follow-up data.
  • Chidamide stopped after less than two cycles.
  • Serious comorbidities that interfere with the efficacy or safety analysis

Who the study is looking for

  • Aged≥18 years
  • Histology-confirmed metastatic CRC (mCRC);
  • ECOG 0\~2
  • At least one efficacy evaluation
  • Life expectancy of at least 3 months.

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

Full criteria on ClinicalTrials.gov

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