At a glance
ClinicalIndex Comparison RecordN/ARecruiting· 6,000 target
Drug / intervention
Not specified
Likely dose
Not stated in record
Key inclusion· 4
- ✓Age at least 18 years
- ✓Pathologically confirmed solid tumor cancer
- ✓Currently receiving immune checkpoint inhibitor treatment
- ✓Able to provide informed consent
Key exclusion· 3
- ✕Age under 18 years
- ✕Hematological malignancies or solid benign tumors
- ✕Mental disorders, drug abuse, or social conditions affecting compliance
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
NCT04766515N/ARecruitingUpdate OverdueCompletion was 34mo agoEnrollment Stalled
Long Recruiting
Update Overdue
Multicenter Observational Prospective Study of Immune Checkpoint Inhibitors in Patients With Solid Neoplasms
In Brief
An observational study for Cancer. Currently recruiting, targeting 6,000 participants across 1 site.
Signals
Enrollment appears stalled
Detailed Summary
This prospective, multicenter observational study included all patients with solid neoplasms who received treatment with immune checkpoint inhibitors (ICIs) in clinical practice, regardless of tumor type, tumor stage, type of immunotherapy, or treatment lines. This study aimed to assess the use, effectiveness, and safety of ICIs for solid neoplasms in real-world populations, which can provide insights into clinical decisions associated with the use of ICIs for the treatment of cancer patients in the real-world setting.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsCancer
CountriesChina
Collaborators--
Timeline
N/ARecruiting
2021202220232024202520262027
Enrollment StartSep 2020
First PostedFeb 2021
Primary CompletionAug 2023
TodayJul 2026
Study CompletionAug 2027
First PostedFeb 23, 2021
Enrollment StartSep 1, 2020
Primary CompletionAug 31, 2023
Study CompletionAug 30, 2027
TodayJul 2, 2026
Enrollment to primary: 3 yearsPosted 5.4 years ago