Trilaciclib Combing Chemotherapy in the Neoadjuvant Treatment of Osteosarcoma
Recruiting now · Phase 2
Conditions studied: Osteosarcoma
In brief
To evaluate the clinical application value in bone marrow protection of Trilaciclib in the neoadjuvant treatment of stage II/III classic osteosarcoma in combination with pirarubicin and lobaplatin.
Key facts
- Study ID
- NCT06714383
- Run by
- Peking University People's Hospital
- People needed
- 50
- Starts
- 2024-11-13
- Expected to finish
- 2025-11-01
- Last updated by the study team
- 2024-12-03
Who can join
Age: 14 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Written informed consent signed;
- Classic osteosarcoma confirmed by histopathology (high grade);
- Newly diagnosed stage Ⅱ-Ⅲ based on Enneking staging criteria;
- Planned to receive neoadjuvant chemotherapy;
- Measurable disease on CT by RECIST 1.1.
- No antitumor system therapy received;
- ECOG 0-1
- Adequate organ function.
- Females of childbearing potential as well as males and their partners must agree to use an effective form of contraception during the study and for 6 months following the last dose of study medication.
You may not qualify if…
- History of malignancies of other type;
- Allergic to study agent;
- History of psychotropic substance abuse, alcohol or drug use;
- The researchers considered inappropriate to join the study of any cause.
Where it is running
- Peking University People's Hospital — Beijing, Beijing Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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