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A Multi-Cohort, Open-Label, Exploratory Clinical Study of Trilaciclib in Myeloprotection in First-Line Combination Chemotherapy Regimens for Advanced Solid Tumors

A Multi-Cohort, Open-Label, Exploratory Clinical Study of Trilaciclib in Myeloprotection in First-Line Combination Chemotherapy Regimens for Advanced Solid Tumors

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082382
Enrollment
Unknown
Registered
2024-03-27
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Advanced solid tumors

Interventions

test group:Trilaciclib combined with chemotherapy

Sponsors

Department of Thoracic Oncology, Cancer Center, Bethune Hospital, Shanxi
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Signed written informed consent before enrollment; 2. Aged > 18 years old, male or female; 3. Pathological examination confirmed the diagnosis of malignant tumors, chemotherapy-based treatment is required, and first-line treatment; 4. ECOG score = 0 points, expected survival = 3 months, follow-up observation for more than 3 months; 5. Blood routine, liver and kidney function, myocardial enzymes and ECG showed no significant abnormalities; 6. Subjects voluntarily joined this study, good compliance, with safety and survival follow-up.

Exclusion criteria

Exclusion criteria: 1. allergic to biological agents; 2. received any cytotoxic chemotherapy or PD-1/PD-L1 inhibitor treatment = 14 days before the first dose of study drug (if relevant); 3. received any study drug = 30 days or = half-life (whichever is longer) before the first dose of study drug; 4. had poor healing factors such as edema, ischemia, and tension at the anastomotic stoma; 5. complete intestinal obstruction; 6. severe cardiovascular disease; 7. infectious disease; 8. bleeding tendency or coagulation dysfunction; 9. unstable vital signs; 10. cachexia; 1.the investigator believes that it should be excluded from this study, for example, in the investigator 's judgment, the subject has other factors that may force the study to terminate halfway, such as other serious diseases (including mental illness) requiring concomitant treatment, severe laboratory abnormalities, accompanied by family or social factors, which will affect the safety of the subject, or the collection of data and samples

Design outcomes

Primary

MeasureTime frame
Incidence of SN;Incidence of FN;

Secondary

MeasureTime frame
ORR;Bone marrow protection ;

Countries

China

Contacts

Public ContactHuijing Feng

Shanxi Bethune Hospital

14251244@qq.com+86 187 3417 7149

Outcome results

None listed

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