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Studies reveal that 9.5% of the global population is affected by liver fibrosis, with males having a higher prevalence of getting affected than females. The prevalence in males is around 10.6% while 5.4% of females may develop the condition once in a lifetime. Moreover, the prevalence increases with age. Therefore, there is a significant emphasis on developing quality medications that help in disease management effectively.
The Liver Fibrosis Drug Pipeline Insight Report by Expert Market Research gives comprehensive insights into liver fibrosis drugs currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for Liver fibrosis. The report includes the analysis of over 100 pipeline drugs and 50+ companies. The liver fibrosis pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials including their adverse effects on patients suffering from liver fibrosis.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration and ongoing product development activities related to liver fibrosis.
Liver fibrosis involves the formation of scar tissues in large amounts, formed as a response to repairing and replacing damaged liver cells. There are different levels of liver fibrosis which are primarily based on the degree of liver damage. The condition does not have many symptoms in the mild to moderate stages. As the patient progresses, they may encounter symptoms like appetite loss, difficulty thinking clearly, fluid buildup in the legs or stomach, jaundice (where the skin and eyes appear yellow nausea, unexplained weight loss or weakness.
Nonalcoholic fatty liver disease (NAFLD) is the most common category of liver fibrosis, followed by alcoholic liver disease, which is due to long-term excesses of drinking alcohol. The treatment varies based on the cause of illness and the symptoms of the patient. Some of the specific treatment alternatives include ACE inhibitors, direct-action antivirals, PPAR-alpha agonists and antifibrotics. Several universities and pharmaceutical companies are collaborating to develop high-efficacy drugs that manage the condition effectively. In March 2024, the United States FDA granted approval to Rezdiffra (resmetirom) for treating adults with noncirrhotic non-alcoholic steatohepatitis (NASH) with moderate to advanced liver scarring (fibrosis). Such approvals indicate a promising landscape for the drugs in the disease pipeline.
This section of the report covers the analysis of liver fibrosis drugs based on several segmentations including:
By Phase
By Drug Class
By Route of Administration
The report covers phase I, phase II, phase III, phase IV, and early phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II covers a major share of the total clinical trials for liver fibrosis. There are around 334 drugs in phase II of liver fibrosis drugs.
The drug molecule categories covered under liver fibrosis pipeline analysis include peroxisome proliferator-activated receptors (PPAR)-alpha agonists, ACE inhibitors, hepatotropic drugs and others. The report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for liver fibrosis.
The EMR report for the liver fibrosis drug pipeline covers the profile of key companies involved in clinical trials and their drugs under development. Below is the list of a few players involved in Liver fibrosis clinical trials:
Major drugs currently in the drug pipeline are as follows:
Tirzepatide
Previously approved for treating type 2 diabetes, Eli Lilly's metabolic disorder medication tirzepatide, currently under phase 2 clinical trial of a 52-week study demonstrated high efficacy against nonalcoholic steatohepatitis (NASH) with no worsening of the liver fibrosis.
ALG-055009
Aligos Therapeutics is conducting a Phase 2a study to investigate the safety, tolerability, efficacy, pharmacokinetics, and pharmacodynamics of oral (PO) daily (QD) doses of ALG-055009 (soft gelatin capsule) for 12 weeks. The study enrols 100 patients and is expected to be completed by December 2024.
The Liver Fibrosis Drug Pipeline Insight Report provides a strategic overview of the latest and future landscape of treatments for liver fibrosis. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into market trends, regulatory environments, and potential growth opportunities within liver fibrosis pipeline insights.
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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Scope of the Report |
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Drug Pipeline by Clinical Trial Phase |
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Route of Administration |
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