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Study on the dominant population of Quxie Capsule in different clinical pathways of metastatic colorectal cancer

Study on the dominant population of Quxie Capsule in different clinical pathways of metastatic colorectal cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053874
Enrollment
Unknown
Registered
2021-12-01
Start date
2021-12-20
Completion date
Unknown
Last updated
2022-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

colorectal cancer

Interventions

Group 1:Standard chemotherapy + Quxie Capsule
Group 2:Maintenance treatment + Quxie Capsule
Group 3:Single drug chemotherapy or targeted therapy + Quxie Capsule
Group 4:Simple TCM treatment + Quxie Capsule

Sponsors

Xiyuan Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 18 years or above, gender is not limited; 2. Pathologically diagnosed as colorectal cancer; 3. The clinical stage is IV; 4. ECOG 0-2 points; 5. Expected survival period >= 3 months; 6. There are measurable lesions that meet the RECIST 1.1 criteria; 7. Voluntarily join the study and sign the informed consent; 8. Those who are expected to have good compliance can follow up the curative effect and adverse reactions according to the program requirements.

Exclusion criteria

Exclusion criteria: 1. Diarrhea > 3 times/day, or grade II and above diarrhea (CTCAE v4.03 classification); 2. Combined with severe cardiovascular system complications, cerebrovascular system complications, active hepatitis, severe liver and kidney dysfunction; 3. There are various factors that affect the absorption of oral drugs, such as inability to swallow and intestinal obstruction; 4. Any unstable situation or situations that may jeopardize the safety of patients and their compliance with the study, such as those with severe mental illnesses such as schizophrenia; 5. Patients who are about to or are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
Progression free survival;Disease control rate;Objective response rate;

Countries

China

Contacts

Public ContactYang Yufei
yyf93@vip.sina.com+86 10 62835678

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026