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NCT Number: NCT07131280

National Collaborative Centre for Hepatic Regenerative Medicine (NC-CHRM): Single vs Repeated Cycle of Granulocyte Colony-Stimulating Factor (GCSF) & Darbepoetin in Early Decompensated Cirrhosis

Chronic liver disease is a growing health concern, with limited access to liver transplants. This study addresses the urgent need for alternatives by exploring regenerative therapies, like G-CSF, to boost the liver's natural repair. The goal is to develop safe, effective, and accessible treatments for patients who cannot undergo transplant.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

The incidence of deaths from chronic liver diseases (CLD) and cirrhosis are rapidly increasing globally, including India. Liver transplant is the only curative option. Unfortunately, transplant is often not feasible. There is a need for nearly 100,000 liver transplants every year in India, though, only about 2,500 transplants are being done at present across the country. There is therefore, a huge unmet need of developing non-transplant options for chronic liver disease patients. In this regard emerging science of regenerative therapy holds great promises but therapeutic benefit of these therapies is limited due to lack of clinical validation.

Novelty: Cirrhosis as a result of hepatitis B and C can regress with effective antiviral therapy. Therapeutic options for patients with cryptogenic or alcoholic cirrhosis are, however, limited. With limited options for transplant. Liver failure is failure of regeneration hence, potentiating native liver repair and regeneration can serve as potential non-transplant approaches. Growth factors {like GCSF, darbepoetin (EPO) have shown survival benefits with improve liver repair and regeneration in clinical trials by us (Gastroenterology 2012, 2015, Liver Int. 2019; Hepatology 2021) and others, however the effect is transient. In the proposed National Collaborative Centre for Hepatic Regenerative Medicine (NC-CHRM) we will use this novel regenerative medicine approaches GCSF therapy (for management of chronic liver failure) to develop safe and effective regenerative therapy clinical protocol for transplant free management of liver failure in cirrhosis. Using integrated cellular, molecular and functional analysis we will also establish their mechanism of action and identify biomarker to access therapeutic response.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Early decompensated cirrhosis patients with MELD <16

Exclusion criteria

  • Patients with age less than 18 years or more than 65 years
  • Patients with Grade III ascites
  • CHILD C cirrhosis
  • Patients with a known focus of sepsis; spontaneous Bacterial Peritonitis (SBP)
  • variceal bleeding in past 3months
  • Hepatocellular Carcinoma (HCC) or other malignancy
  • Acute Kidney Injury (AKI) with serum Creatinine >1.5 mg/ dl, multi-organ failure, grade 3 or 4 Hepatic Encephalopathy (HE),
  • HIV seropositivity
  • Medically uncontrolled essential hypertension
  • Pregnancy
  • Viral etiology of liver disease
  • Co-existent Hepatitis B, Hepatitis C, HIV
  • Chronic kidney disease
  • Lack of informed consent

Treatment and study plan

GCSF

Drug

G-CSF will be given at a dose of 5 μg/kg s/c at days 1, 2, 3, 4, 5 and then every third and 7th day till day 30

Darbepoetin

Drug

Darbepoetin will be given s/c at dose of 40mcg once a week for 1 month

Standard Medical Treatment

Other

Standard Medical Treatment

Primary outcomes

  1. Transplant-free survival of GCSF + darbepoetin in patients with early decompensated cirrhosis in both groups.

    Time frame: 3 year

Secondary outcomes

  1. Transplant-free survival

    Time frame: 6-month, one year, 2 year and 3 year

  2. Proportion of patient developed new-onset of Liver Related Event (such as ascites, hepatic encephalopathy , acute kidney injury, bleed and sepsis) or show mortality in both the groups

    Time frame: 6-month, one year, 2 year and 3 year

  3. Cumulative incidence of sepsis, acute kidney injury or secondary organ dysfunction in both groups

    Time frame: 6-month, one year, 2 year and 3 year

  4. Cumulative incidence of second decompensation

    Time frame: 6-month, one year, 2 year and 3 year

  5. Improvement in liver disease severity indices, including the Child-Turcotte-Pugh (CTP) score (ΔCTP).

    Time frame: 6-month, one year, 2 year and 3 year

  6. Improvement in liver disease severity indice like Model for End-Stage Liver Disease (MELD) score (ΔMELD).

    Time frame: 6-month, one year, 2 year and 3 year

  7. Proportion of patients completing treatment without major adverse effects

    Time frame: 6-month, one year, 2 year and 3 year

    Adverse effects will be graded in accordance to CTCAE

  8. Impact on liver injury (assessed by AST and ALT levels in blood).

    Time frame: 6-month, one year, 2 year and 3 year

  9. Impact on fibrosis (evaluated using Masson's Trichome stain and the Enhanced Liver Fibrosis [ELF] score).

    Time frame: 6-month, one year, 2 year and 3 year

  10. Impact on regeneration (measured by plasma Alpha-Fetoprotein levels).

    Time frame: 6-month, one year, 2 year and 3 year

  11. Impact on bone marrow stem cell reserve (CD34⁺ cell count in peripheral blood)

    Time frame: One year, 2 year and 3 year

Study contacts

Contact information is provided by the study sponsor or research team.

Dr. Anupam Kumar, PhD

CONTACT

[email protected]

01146300000

Fagun Sharma, M.Sc.

CONTACT

[email protected]

01146300000

Sponsors and collaborators

Lead sponsor

Institute of Liver and Biliary Sciences, India

Other

Collaborators

  • Indian Council of Medical Research

Registry information

Official study title

National Collaborative Centre for Hepatic Regenerative Medicine(NC-CHRM): To Study the Efficacy of Single vs Repeated Cycle of GCSF+ Darbepoetin in Long Term Transplant Free Management of Patient With Early Decompensated Cirrhosis

Acronym: NC-CHRM

Important dates

Study start
2025
Primary completion
2031
Study completion
2031
First posted
Aug 20, 2025
Registry last updated
Aug 20, 2025

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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