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Establishment and Real-World Application of an Adverse Reaction Monitoring System for Targeted therapy of Antitumor Drugs

Establishment and Real-World Application of an Adverse Reaction Monitoring System for Targeted therapy of Antitumor Drugs

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124485
Enrollment
Unknown
Registered
2026-05-13
Start date
2024-09-11
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

cancer

Interventions

Observation group:none

Sponsors

Jiangnan University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Male or female; 2. Age >=18 years at the time of signing the informed consent; 3. Clinically and pathologically confirmed malignant tumor (solid tumor and/or hematologic tumor); 4. Clinical judgment that the use of targeted anti-tumor drugs can benefit the patient, and the patient has received at least one dose of molecular targeted therapy; 5. Able to undergo long-term follow-up; 6. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Mental abnormalities or speech disorders preventing cooperation with examination or follow-up; 2. Other severe diseases with an expected life expectancy of less than 1 month; 3. Other situations that the researcher deems necessary to exclude.

Design outcomes

Primary

MeasureTime frame
Adverse events after medication use;

Secondary

MeasureTime frame
Disease progression;Adverse reaction outcome;The direct or indirect medical costs resulting from the occurrence of AE;

Countries

China

Contacts

Public ContactYongjuan Ding

Jiangnan University Affiliated Hospital

2649570095@qq.com+86 510 6808 9178

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026