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Clinical Trials in China / NCT07131644
Starting soon Phase 2

Sirolimus Discontinuation Strategies in Kaposiform Hemangioendothelioma

NCT07131644 · tracked via the Priya Life Science China tracker
Sponsor
West China Hospital
Phase
Phase 2
Started
2025-09-13
Last updated
2025-09-08

Condition(s) studied

Kaposiform Hemangioendothelioma

Investigational drug(s) / intervention(s)

Sirolimus →

Sirolimus: Comparison of different sirolimus discontinuation strategies.

Study summary

Sirolimus has demonstrated efficacy in the treatment of kaposiform hemangioendothelioma (KHE); however, a high rate of rebound growth following discontinuation has been reported, highlighting the clinical importance of establishing an appropriate withdrawal regimen.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * KHE patients who have received sirolimus treatment and met the criteria for drug discontinuation. * With evaluable clinical or imaging parameters to monitor disease activity or recurrence. * Patients or their guardians are able to understand the study and provide written informed consent. * Hematologic and hepatic/renal function meet the safety criteria for drug administration. Exclusion Criteria: * Patients who are unable to comply with the follow-up or treatment schedule, potentially affecting the integrity of study data.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
West China Hospital of Sichuan University Chengdu Sichuan

More West China Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07131644 on ClinicalTrials.gov ↗ ← All trials in China