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相关临床试验
5
0 进行中
药物批准
2
批准总数
监管机构
1
监管机构数
成立时间
2010
招募中
20.0%
Unknown
4
80.0%
NMPA
National Medical Products Administration
- A phase I dose-escalation trial determined the maximum tolerated dose of pegylated liposomal doxorubicin (PLD) at 50 mg/m² when combined with ifosfamide for advanced soft tissue sarcoma treatment. - The combination demonstrated manageable toxicity with grade 3/4 hematological adverse events being most common, including leukopenia (86.96%) and neutropenia (82.61%). - Among 12 patients who continued treatment beyond dose-finding, the overall response rate reached 33.33% with a disease control rate of 83.33%. - The study showed no cardiotoxicity events, suggesting PLD offers a safer cardiac profile compared to conventional doxorubicin-based regimens.