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Pharmacokinetic Study of Melphalan in Pediatric Hematopoietic Stem Cell Transplantation

Phase 1
Recruiting
Conditions
Hematopoietic Stem Cell Transplantation
Interventions
Registration Number
NCT04937634
Lead Sponsor
Seoul National University Hospital
Brief Summary

This is an investigator-initiated clinical trial to analysis melphalan pharmacokinetics in pediatric hematopoietic stem cell transplantation patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  • The patient who will receive a conditioning regimen including melphalan as a part of hematopoietic stem cell transplantation (HSCT).
  • Age is below 19 at the time of diagnosis of a disease which is HSCT indication
  • Written Study Informed consent and/or assent from the patient, parent, or guardian
Exclusion Criteria
  • Female patients who are pregnant or breast feeding
  • Study treatment would deteriorate patient's disease.
  • The patient may have problems with study participation due to a psychotic disorder.
  • Any condition that would, in the Investigator's judgement, interfere with participation in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
MelphalanMelphalan-
Primary Outcome Measures
NameTimeMethod
Melphalan concentrationpre dose, within 5 minutes from end of melphalan infusion(EOI), 40 minutes from EOI, 70 minutes from EOI, 170 minutes from EOI

Analysis: Half lite (T1/2)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Seoul National University Hospital

🇰🇷

Seoul, Korea, Republic of

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