Institute of Liver & Biliary Sciences
New Delhi, 110070, India
NCT Number: NCT07131280
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.
Trial opening soon.
Get Notified18 year–65 year
All sexes
Interventional
Not applicable
New Delhi, 110070, India
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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 will be given s/c at dose of 40mcg once a week for 1 month
Standard Medical Treatment
Time frame: 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Adverse effects will be graded in accordance to CTCAE
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: 6-month, one year, 2 year and 3 year
Time frame: One year, 2 year and 3 year
Contact information is provided by the study sponsor or research team.
Dr. Anupam Kumar, PhD
CONTACT
Fagun Sharma, M.Sc.
CONTACT
Institute of Liver and Biliary Sciences, India
Other
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
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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