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NCT Number: NCT04522869

Umbilical Cord Derived Mesenchymal Stem Cell (UC -MSC) Transplantation for Children Suffering From Biliary Atresia

Biliary atresia (BA) is the most frequent cause of chronic cholestasis in neonates, accounting for at least 50% of pediatric liver transplantation. BA incidence is estimated to range from 1:5000 to 1:19000 live births. All patients will die due to complications of liver cirrhosis if the operation is not performed. Recently, mesenchymal stem cell (MSC) transplantation has been found as a promising therapy for liver cirrhosis in adults. Bone marrow-derived stem cell transplantation was also performed successfully for children with BA. Compared to MSC isolation from bone marrow, isolating MSCs from umbilical cord (UC) tissue is a less invasive procedure.

Furthermore, UC-derived MSCs (UC-MSCs) have been demonstrated to be safe and effective for liver cirrhosis in adults and different pediatric diseases, including liver cirrhosis due to primary biliary cirrhosis. The investigators will compare the outcomes of 17 Kasai operated BA patients who receive UC-MSC transplantation to 17 BA patients who only undergo Kasai operation. Two transplantations of UC - MSCs will be performed via the hepatic artery: the first transplant will be performed at baseline, and the second one will be performed 6 months later with a dosage of 1 million MSCs per kg of body weight. The frequency and severity of the adverse events or serious adverse events associated with UC-MSC injection at 72 hours post-injection will be used to assess the safety. The efficacy of the therapy will be measured using Pediatric End-Stage Liver Disease (PELD) score, liver function, and liver biopsy. This study would open a novel cell therapy to improve outcomes of patients with BA.

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Key information

Age range

5 month–2 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Vinmec International Hospital Times City, Hanoi, Vietnam

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About this study

The study protocol was approved by the Vinmec International Hospital Ethics Committee, and National Ethics Committees. The stem cell products are conducted in accordance with (GMP) requirements and Good Clinical Practice (GCP). All patients and primary caregivers will receive a written consent form, a cover letter and a clear explanation of the safety issues, potential risks and benefits, and the procedure involved. Moreover, patients will be provided the updated results related to disease and the study during conducting the study and will be fully funded by the project.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children diagnosed with liver cirrhosis due to biliary atresia after Kasai's operation
  • From 5 months to 2 years old
  • Weight ≥ 6 kg
  • Patients with manifestation of cirrhosis on liver biopsy during Kasai's operation.
  • Parents or primary caregivers signed the informed consent form.

Exclusion criteria

  • Under 6kg or over 2 years old
  • Coagulation disorders
  • Allergy to anesthetic agents
  • Active infections

Treatment and study plan

Umbilical Cord Derived Mesenchymal Stem Cell (UC -MSC) Transplantation

Biological

Umbilical Cord Derived Mesenchymal Stem Cell (UC -MSC) Transplantation for Children Suffering From Liver Cirrhosis Due to Biliary Atresia

Primary outcomes

  1. The change of PELD scores during study

    Time frame: baseline, 3 months, 6 months, 9 months, 12 months

    The PELD score is calculated using the following formula:

    PELD Score = 0.480 * ln (Bilirubin in mg/dL) + 1.857 * ln (INR) - 0.687 * ln (Albumin in g/dL) + 0.436 if the patient is <1 year old + 0.667 if there growth failure

  2. The change of albumin (Liver function)

    Time frame: up to the 12-month period following treatment

    Levels of albumin (g/dL)

  3. The change of total bilirubin (Liver function)

    Time frame: up to the 12-month period following treatment

    Total bilirubin level (mg/dL)

  4. The change of prothrombin time

    Time frame: up to the 12-month period following treatment

    Prothrombin time (second)

  5. The change of liver biopsy

    Time frame: up to the 12-month period following treatment

    change of liver biopsy

Secondary outcomes

  1. The number of Adverse Events (AE) and Serious Adverse Events (SAE)

    Time frame: baseline, 3 months, 6 months, 9 months, 12 months (time frame: up to the 12-month period following treatment)

    Adverse Events (AE) and Serious Adverse Events (SAE) after MSC transplantation

Sponsors and collaborators

Lead sponsor

Vinmec Research Institute of Stem Cell and Gene Technology

Other

Collaborators

  • Number 2 Children's Hospital, Ho Chi Minh City

Registry information

Official study title

Evaluation Safety and Efficacy of Umbilical Cord Derived Mesenchymal Stem Cell (UC -MSC) Transplantation for Children Suffering From Liver Cirrhosis Due to Biliary Atresia: A Matched Control Prospective Study

Acronym: UCMSCBA

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Aug 21, 2020
Registry last updated
Jun 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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