Clin2
NCT07656909Possibly a fitRecruiting

Comparing low and high dose sirolimus with prednisolone for KHE with KMP

Kaposiform Hemangioendothelioma (KHE)Kasabach Merritt Phenomenon

Treatments studied

Part of Blood & lymphatic, Cancer clinical trials.

This study tests whether a low dose or a high dose of sirolimus (a drug that stops abnormal cell growth) combined with prednisolone (a steroid) works better for children with a rare, aggressive vascular tumor called KHE that also causes low blood platelets (KMP). The goal is to find the safest and most effective dose to help shrink the tumor and improve blood counts.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2/Phase 3
Enrollment
76 people
Ages
1 day to 18 years
Study type
Interventional

Who can take part

  • Your child must be between 0 and 18 years old.
  • Your child must have a confirmed diagnosis of a progressive, unresectable KHE (a type of vascular tumor) that is also causing low blood platelets (KMP).
  • Your child must not be currently needing treatment with corticosteroids for health problems caused by the KHE.
  • Your child's liver, kidney, and bone marrow function must be in a healthy range based on blood tests.
  • Your child must not have a serious infection requiring IV antibiotics, a known immune problem, or a history of cancer.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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