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A prospective, non-interventional, multicenter clinical study to explore the efficacy and safety of camrelizumab in combination with regorafenib in patients with advanced colorectal cancer

A prospective, one-arm, single-center clinical study of thioepipstatin for the prevention of chemotherapy-related neutropenia in nasopharyngeal carcinoma

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027398
Enrollment
Unknown
Registered
2019-11-12
Start date
2019-11-11
Completion date
Unknown
Last updated
2019-11-18

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

Conditions

Colorectal cancer

Interventions

Sponsors

The First Affiliated Hospital of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old, male or female; 2. ECOG PS score is 0 ~ 2; 3. Patients with advanced colorectal cancer diagnosed by histology or cytology (mCRC); 4. Patients with unresectable recurrent solid tumors or who do not tolerate standard chemotherapy; 5. According to RECIST 1.1, at least one measurable target lesion exists; 6. Without intervention in the study, patients can use carillizumab combined with rigafinil in one or more lines; 7. According to imaging judgment (RECIST 1.1 standard), patients who had received the last anti-tumor regimen before enrollment or who had progressed during the treatment; 8. Sign informed consent and agree to collect clinical efficacy and information of patients;

Exclusion criteria

Exclusion criteria: 1. There is a third gap effusion (such as a large amount of hydrothorax and ascites) that cannot be controlled by drainage or other methods, and the clinical therapeutic effect cannot be evaluated; 2. Received radiotherapy, chemotherapy, surgery or other targeted therapy for colorectal cancer within 1 week before the first use of the study drug and did not progress from the previous treatment; 3. Patients with immunodeficiency (such as vitiligo, psoriasis, hypothyroidism requiring hormone replacement therapy, etc.) and patients allergic to experimental drugs; 4. Pregnant or lactating women, patients with fertility who are unwilling or unable to take effective contraceptive measures; 5. The investigator judges other situations that may affect the conduct of the clinical study and the judgment of the study results.

Design outcomes

Primary

MeasureTime frame
PFS;

Countries

China

Contacts

Public ContactJiang Haiping

The First Affiliated Hospital of Zhejiang University

jianghaiping15@163.com+86 15257126683

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026