Analysis of Clinical Trials of New Drugs for Liver Diseases in China.

BACKGROUND: Liver diseases are a major public health concern worldwide, and the development of novel therapeutic drugs is an important research focus. But no overview has been conducted so far on the current research and development for liver-specific drugs in China, and the actual situation regarding the development and evaluation of new drugs in clinical trials.
METHODS: The information of all clinical trials on liver diseases were obtained through the "Pharmaceutical Clinical Trial Registration and Information Disclosure Platform" before December 31, 2020.
RESULTS: A total of 751 clinical trials on liver disease-related drugs were published on the above platform, including 574 chemical drugs, 128 biological products, and 49 traditional Chinese medicine (TCM)/natural drugs. The number of annual registrations has increased on an annual basis. The main indications for these clinical trials are viral hepatitis, liver malignancies, liver abscess, liver transplantation, congenital liver metabolic disease, and other hepatitis-related diseases. Hepatitis B, hepatitis C and liver cancer accounted for 72.4% of the total clinical trials, and the majority are related to generic drug research. There are 103 innovative drugs currently in clinical testing, mainly for hepatitis B, hepatitis C and hepatocellular carcinoma.
CONCLUSION: The stronger macro-control is required for the clinical trials conducted in China, and it is necessary to identify new therapeutic targets and develop novel drugs for the key liver diseases, as well as preventive hepatitis C vaccines, and targeted therapy, TCM/natural drugs and immunotherapy for liver cancer.

Introduction

Liver diseases are a major cause of morbidity and mortality worldwide. More than a million people die every year due to viral hepatitis, which is also one of the most prevalent infectious diseases in China. Hepatitis B accounts for more than 70% of all incidences of viral hepatitis, and 10–20% of chronic hepatitis B cases can progress to liver cirrhosis and 1–5% to liver cancer.1–4 The incidence of liver cancer in China is 36.5/100,000, which is responsible for 418,000 deaths each year, accounting for 50% of the global liver cancer-related mortality.5,6 Given the serious socio-economic consequences of liver diseases, the research and development (R&D) of therapeutic drugs has gained precedence in recent years.

Drug R&D and production is an index of a country’s economic and scientific capabilities. With improvements in living standards and amendments in national health policies, China has significantly increased investment in drug R&D in recent years. Numerous drug clinical trials are registered every year, especially related to liver diseases. However, no overview has been conducted so far on the current R&D for liver-specific drugs in China, and the actual situation regarding the development and evaluation of new drugs in clinical trials. In order to strengthen the supervision and management of drug clinical trials, promote transparency of results, and protect the rights and safety of the participating subjects, the State Food and Drug Administration (SFDA) has established a “Drug Clinical Trial Registration and Information Disclosure Platform” in accordance with the requirements of the World Health Organization (WHO) and international practices. In a 2013 addendum, SFDA stated that all approved clinical trials in China (including bioequivalence and PK trials, and phases I–IV) should be registered and all relevant information logged into .

In this study, we reviewed the clinical trials on liver disease-related drugs published on the above platform before December 31, 2020. Our objective is to gain a better understanding of the current situation regarding the development of new drugs and provide a decision-making basis for further R&D and regulatory guidelines.

Methods

The information of all clinical trials on liver diseases, including viral hepatitis, liver cancer, cirrhosis, non-alcoholic steatohepatitis, etc., entered before December 31, 2019, were extracted. The registration numbers, status, drug name, dosage form, indications, popular test topics, registration date, applicant’s test stage, main investigator, etc. were analyzed.

Results

Overall Situation Analysis

Number of Registrations

As of December 31, 2020, the drug clinical trial registration and information disclosure platform has published the information of 751 clinical trials are concerned with liver diseases, including 574 for chemical drugs (76.4%), 128 for biological products (17.0%) and 49 (6.5%) for Traditional Chinese Medicine (TCM)/natural drugs. Furthermore, 19 of these trials are actively suspended and the remaining 732 are in progress or completed. The latter include 560 trials on chemical drugs, 124 on biological products and 48 TCM/natural drugs.

The number of annual clinical trials registrations for liver diseases has been increasing on a yearly basis, and the number of clinical trial registrations reached 137 in 2020, as shown in Figure 1A. However, the number of clinical trials of TCM/natural medicines in the past 5 years is not exceeding 5 per year (Figure 1A). The spike in clinical trial registration post 2013 could be attributed to policy changes that led to supplementary registrations. Furthermore, 31.2% and 50.9% of the trials on chemical drugs are respectively at Phase I and preclinical stages (bioequivalence and pharmacokinetics testing), whereas 66.1% of the biological products are at phases I and III of testing. In contrast, 50% of the clinical trials of TCM/natural drugs are at Phase II (Figure 1B).

Figure 1

Annual numbers of clinical trials of initiated drug used for liver diseases in China (A); The phase of clinical trials of initiated drug used for liver diseases in China (B).

Distribution of Dosage Form

The different dosage forms of the chemical, biological and TCM/natural drugs are summarized in Figure 2. Most chemical drugs (90.9%) are administered as tablets and capsule, while 40 are injectables. In contrast, 98.4% of the biological products are in the injectable form. The dosage forms of TCM/natural drugs are the most varied, including pills, granules, capsules, tablets and injections. There are few clinical trials on new generation drug delivery systems, including six liposomes and four microspheres, all loaded with chemical therapeutics.

Figure 2

Distribution of dosage forms for clinical trials for liver diseases of chemical drugs, biological products and TCM/natural drugs.

Distribution of Clinical Research Institutions and Applicants

More than 98% of the research institutions listed in the registered clinical trials are located in mainland China, and only nine major research centers are in other countries, such as Spain, the United States and Korea. Moreover, 58.7% of the research centers are concentrated in Beijing, Shanghai, Jiangsu and Jilin province as of December 31, 2020, and a few are situated in northwest China but not in Tibet and Qinghai.

Frequency of Trials

Due to the generic nature of most drugs related to liver disease, several are part of multiple clinical trials. Based on the registration details, 35 drugs are being tested in more than five clinical trials. Tenofovir disoproxil fumarate tablets and tenofovir propofol fumarate tablets have the highest number of trials (30), followed by entecavir tablets (29). Furthermore, more than 10 clinical studies are registered for yimitasvir phosphate capsules, lenvatinib mesilate capsules, sorafenib tosylate tablets, seraprevir potassium tablets and tenofovir alafenamide tablets. For statistical analysis, the different dosage forms of a compound were considered the same drug.

Indigenous Innovation Drugs for Liver Disease

In document No. 51 published in 2016, SFDA classified innovative drugs, defined as those that have not been marketed in China or abroad, contain novel compounds with a clear structure, and with pharmacological effects and clinical value, into a separate group. As shown in Table 1, 103 innovative drugs for liver diseases are currently in clinical testing, and the number of new applications is increasing. Among them, 24 are biological products and 79 are chemical drugs. The indications of innovative drugs in the field of liver diseases are mainly concentrated in the treatment of hepatitis B, hepatitis C, hepatocellular carcinoma, and many types of cancer including liver cancer. In addition, these innovative drugs are also used to treat drug-induced liver injury, viral hepatitis, prevent hepatitis B, liver fibrosis, cirrhosis ascites, prevent hepatitis E, amoeba liver abscess, non-alcoholic steatohepatitis, etc. The statistical analysis of the 103 innovative drugs was conducted on the basis of compounds, resulting in overlapping dosage forms and clinical trials of the same drug.

Table 1

The Indigenous Innovation Drugs for Liver Disease in China Clinical Studies

Indications		Drug Name
Viral hepatitis	Hepatitis B	GLS4-methanesulfonate, isothiafludine, metacavir, pradefovir mesylate, HS-10234, QL-007, TQ-A3334, therapeutic hepatitis B vaccine, recombinant human serum albumin/interferon alpha 2a fusion protein for injection, hepalatide, tyrophentide, therapeutic injection of hepatitis B adenovirus, HH-003, recombinant human serum albumin-interferon alpha 2a fusion protein injection (yeast), imidol hydrochloride, APG-1387, octadecyloxyethyl-tenofovir, STSG-0002, TVAX-008, TQA3729, PA1010, KL060332, HRS9950, HRS5091, HEC121120, GST-HG141, GST-HG131, ASC22
	Hepatitis C	Yimitasvir phosphate, serarivir potassium, ASC16, furaprevir, coblopasvir, SH229, ASC08, fupitavir, amphibavir, HEC74647PA, ZN6168, HEC110114, kangdaprevir sodium, ZN2007Na, TQ-A3326, ASC18
	Hepatitis B and C	Y type PEGylated recombinant human interferon α2b injection
	Hepatitis	Polyethylene glycol new integrated interferon mutant injection, recombinant human serum albumin/interferon α2b fusion protein for injection
	Prevention of hepatitis B	Recombinant hepatitis B vaccine containing pre-S antigen (Pichia pastoris)
	Prevention of hepatitis E	Recombinant hepatitis E vaccine
Liver cancer	Liver cancer	SHR-1210, ursolic acid nanoliposomes, tyroserleutide, donafenib tosylate, brivanib alaninate, tislelizumab, recombinant humanized anti-PD-1 monoclonal antibody injection, TQB2450, chlorogenic acid, para-toluenesulfonamide, metatinib trometamol, MB07133, lucitanib, chiauranib, ATG-008, Hemay102, recombinant human anti-human epidermal growth factor receptor monoclonal antibody injection, ZSP1241, dicycloplatin, AK105, angiogenesis aprotinin, sintilimab, recombinant anti-VEGF humanized monoclonal antibody injection, EMB-01, GST-HG161, HJ197, recombinant human PD-1 antibody herpes simplex virus, CS1003 monoclonal antibody, recombinant human calmodulin B for injection, 4-{4-3-fluorophenoxy} pyridine-2-carboxamide, detorsertib, QL1604, DX1002, AK104, ACT001
	Intrahepatic cholangiocarcinoma	Famitinib malate, HMPL-453 tartrate
Nonalcoholic steatohepatitis	Nonalcoholic steatohepatitis	ZSP1601, ZSP0678, TQA3563, HEC96719, SYHA1805, SH2442, HS-10356, ASC41
Liver fibrosis	Liver fibrosis in chronic viral hepatitis B	Hydronidone
	Hepatic fibrosis	Fluorofenidone
Others	Cirrhotic ascites	Recombinant human albumin injection
	Amoebic liver abscess	Ornidazole
	Liver function damage	SHR6390, SHR3680
	Acute drug-induced liver injury	Bicyclol

Analysis of Clinical Indications

Distribution of Clinical Indications

The indications of clinical trials are viral hepatitis, liver malignant tumor, liver abscess, liver transplantation, congenital liver metabolic disease and other hepatitis-related diseases. A total of 438 clinical trials are related to viral hepatitis, especially hepatitis B and C that account for 93% of viral hepatitis-related diseases. In addition, there are 16 trials for preventive vaccines against hepatitis A, B and C, and 9 for hepatitis B with liver fibrosis. Liver malignancies are the focus of 172 clinical trials, of which 123 are being conducted only on liver cancer patients, and 45 have included patients with liver cancer, stomach cancer and lung cancer. Furthermore, drugs for liver abscess, liver transplantation, congenital liver metabolic disease, and other hepatic diseases like nonalcoholic steatohepatitis, alcoholic fatty liver and liver fibrosis are being tested in 19, 15, 3 and 84 clinical trials respectively (Figure 3). Diseases of the digestive tract and metabolism, systemic infections, cardiovascular disorders often have liver-related complications. Therefore, the liver-specific effects of drugs related to the above are also under investigation. For example, ornidazole and levornidazole are used to treat infections, and are effective against amoebic liver abscess as well. Likewise, torsemide and spironolactone can be used for treating cirrhotic ascites.

Figure 3

The distribution of clinical indications for liver diseases.

Clinical Research Status of Drugs for Treating Hepatitis B

The currently administered drugs for treating chronic hepatitis B(HBV) virus are classified into two categories: 1) immunomodulators including interferon alpha (IFNα), peg-IFNα, etc and 2) direct-acting antiviral agents, including nucleoside analogs and nucleotide analog prodrugs, such as lamivudine, telbivudine, adefovir dipivoxil, tenofovir disoproxil fumarate, etc.

Immunomodulators inhibit viral replication by induce an antiviral immune response by targeting specific checkpoints and immune cells, such as activating the JAK-STAT signaling pathway.7–9 Such drugs have the advantages of high efficacy, high tolerance and low side effects.10,11 IFNs are broad-spectrum antiviral agents that bind to the specific receptors on immune cell surface, and trigger the production of antiviral proteins such as 2ʹ5’ oligoadenylate synthase (2ʹ5’AS), protein kinase, phosphate diphosphate esterase, etc, which inhibit synthesis of viral nucleic acid and proteins.12,13 Although IFN is absorbed quickly, it has an extremely short half-life in circulation, and has extensive side effects. Conjugation of IFN with PEG can extend its half-life, and several clinical trials are underway on the effects of Peg-IFN. In addition, thymosin-α1 (Tα1) increases IL-2 synthesis, and upregulates the IL-2 high-affinity receptor on T cell precursors, which then effectively eliminate HBV. Tα1 also reduces the cytotoxic effect of tumor necrosis factor (TNFα), and is therefore a promising agent for hepatitis B treatment.14

Nucleoside analogs act directly on viral reverse transcriptase and block HBV replication, which do not directly inhibit cccDNA, viral transcription or translation, but instead block the reverse transcription activity of HBV polymerase, thereby inhibiting the synthesis of viral DNA from pre-genomic RNA. They compete with normal nucleotides during replication of viral DNA, and terminate DNA chain synthesis. Octadecyloxyethyl-tenofovir is a fat-soluble polymer derivative of tenofovir synthesized by adding long-chain octadecyloxyethyl, which significantly improves the permeability and absorption rate. Furthermore, in vitro pharmacokinetic and bioavailability tests showed a stronger inhibitory activity of octadecyloxyethyl-tenofovir compared to tenofovir. Nucleocapsid inhibitors including GLS4-methanesulfonate, RO7049389, JNJ-56136379, etc, induce defective nucleocapsid assembly by regulating core proteins at multiple points in the virus life cycle. The clinical trials of direct-acting antiviral agents are summarized in Table 2.

Table 2

Clinical Trials of Chemical Drugs Used to Treat Hepatitis B and Its Mechanism in China

Drug Name	Mechanism
Isothiafludine	Induces abnormal assembly of HBV core protein to form a vacuole nucleocapsid without viral nucleic acid
Metacavir	Compete with HBV polymerase substrate deoxyguanosine triphosphate, thereby inhibiting the HBV-DNA replication process
GLS4-methanesulfonate	Interfere with HBV virus capsid assembly, inhibit HBV DNA synthesis and replication
Imidol hydrochloride	It may inhibit the membrane fusion between the virus and liver cells, inhibit HBV-DNA replication, and immunomodulate
Pradefovir mesylate	Adefovir Prodrug, competitively incorporation with adenylate into the viral DNA chain, which inhibits viral replication
Tyrophentide	It can regulate the calcium-Pyk2 signaling pathway and p21 factor downstream of HBV replication, thereby inhibiting the expression of cccDNA
Hepalatide	Through specific binding to HBV hepatocyte infection receptor NTCP to blocking HBV infection
HS-10234	Tenofovir prodrugs of monophosphoramide monoesters
Tenofovir alafenamide semi-fumarate	Tenofovir disoproxil fumarate prodrug
QL-007	Capsid inhibitors, blocking viral capsid assembly
APG-1387	It can make the liver cells infected by the virus have better sensitivity to the immune-mediated cells, thereby eliminating the hepatitis B virus DNA and antigens mediated by specific T cells
RO7020531	It is a selective TLR7 agonist, which enhances the body’s host immune activity to eliminate hepatitis B virus
RO7062931	Hepatocyte uptake mediated by asialoglycoprotein receptor (ASGPR) can lead to hybridization of SSO LNA and HBV mRNA, followed by RNAse H-mediated degradation
GSK3389404	Viral protein inhibitors. By binding to hepatitis B virus mRNA and then preventing its transformation into hepatitis B virus protein, and inhibit hepatitis B virus replication
Octadecyloxyethyl-tenofovir	Introducing octadecoxyethyl into tenofovir to enhance its liposolubility and improve bioavailability
RO7049389	Allosteric modulator of HBV core protein. By inducing the formation of abnormal HBV core aggregates, leading to defective capsid assembly to inhibit HBV replication, and possibly restore the host’s immune response to HBV
JNJ-56136379	HBV capsid protein assembly inhibitor
TQ-A3334	Highly selective TLR7 agonist that inhibits HBV by activating TLR7 to induce specific cytokines and chemokines
ABI-H2158	HBV core protein allosteric modulator, blocking hepatitis B virus capsid protein assembly
KL060332	Hepatitis B virus capsid inhibitor
HRS9950	Toll-like receptor 8 agonists
HRS5091	Nucleocapsid protein modulators
HEC121120	Undefined mechanism
GST-HG141	Viral core protein inhibitors
GST-HG131	Hepatitis B surface antigen expression inhibitors
ASC22	Antibody-dependent cell cytotoxicity; programmed cell death-1 ligand-1 inhibitors; T lymphocyte stimulants
VIR-2218	Hepatitis B virus replication inhibitors; RNA interference
BRII-179 (VBI-2601)	B cell modulators; T lymphocyte modulators

Exclude the commercialized drugs as indications.

In addition, peptides and vaccines are also promising drugs for hepatitis B treatment. Vaccines reverse immunotolerance and induce a cellular immune response. Clinical studies on intravenous injection of hepatitis B human immunoglobulin (pH4), hepatitis B vaccine, double plasmid HBV DNA vaccine and hepatitis B adenovirus injection are currently ongoing. Hepalatide is a new peptide drug that binds to the sodium taurocholate cotransporting polypeptide (NTCP) on hepatocytes,16 which blocks the interaction of HBV to its specific receptor and prevents virus entry.

Clinical Research of Drugs for Treatment of Hepatitis C

In 2015, AASLD, EASL and APASL updated their guidelines for the prevention and treatment of chronic hepatitis C(CHC), and especially emphasized the use of direct antiviral agents (DAAs) that target NS3/NS4 protease, NS5A, NS5B RNA and NS4B and NS3 helicase proteins encoded by hepatitis C virus (HCV).17,18 The DAAs currently under development are summarized in Table 3.

Table 3

The Clinical Drugs and Mechanism for Treatment of Hepatitis C in China

Mechanism	Drugs
NS3/4A protease inhibitor	TMC435
	Furaprevir
	Serarivir potassium
	ASC08
	Kangdaprevir sodium
NS5A protease inhibitor	Yimitasvir phosphate
	Coblopasvir
	Ravidasvir
	Fupitavir
	ZN6168
NS4B protease inhibitors	Amphihevir
NS5B protease inhibitors	Holybuvir
NS3 protease inhibitors	ZN2007Na
Combination drugs	ASC18 ABT-450/ritonavir/ABT-267
Broad-spectrum antiviral	Ribavirin

Exclude the commercialized drugs as indications.

NS3/4A protease inhibitors were the first DAAs to be developed for treating chronic hepatitis C. The combination of NS3/4A protease inhibitors and standard treatment regimens increased the cure rate of hepatitis C by ≥30%. Serarivir potassium, furaprevir, and kangdaprevir sodium are innovative new drugs developed in China. The clinical trial results and therapeutic effects of these agents have not been announced so far.

NS5B RNA polymerase inhibitors include both nucleoside and non-nucleoside inhibitors.19 The former directly target the active site of the polymerase, and non-nucleoside inhibitors target non-active sites and alter enzyme conformation, thereby inhibiting its function. Holybuvir is the first self-developed nucleoside HCV NS5B inhibitor to enter phase II/III clinical trials in China.

The NS5A RNA polymerase inhibitor regulates both virus replication and virion assembly.20 Novel NS5A inhibitors including yimitasvir phosphate, coblopasvir, fupitavir, ZN6168, etc, are currently being developed in China. Yimitasvir phosphate was first synthesized in 2012, and its structure is similar to ledipasvir and velpatasvir. Coblopasvir activity against GT-1-6 HCV and GT-3a HCV are respectively equivalent to and stronger than that of DCV. ZN6168 inhibits the replication of all six subtypes of NS5A virus, and its inhibitory effect against the NS5A-3a subtype replicon is 10 times more potent than that of DCV.

Amphibavir is an HCV NS4B inhibitor that was developed in China, and is currently the only indigenous hepatitis C NS4B-targeting drug in the clinical testing stage.21 It inhibits viral replication by blocking the interaction between the arginine-rich region of NS4B and the negative strand viral RNA. Finally, pegylated recombinant integrated IFN variant injection, Y-pegylated recombinant human IFN-α2b injection and RopegIFN-α2b (P1101) injection are the anti-hepatitis virus IFN drugs currently in clinical development.22

Clinical Research on Drugs for Liver Cancer

The chemical drugs and its mechanism for liver cancer as listed in Table 4. Most ongoing clinical trials are focused on molecular targeted therapy and immunotherapy, and relatively few on chemotherapeutics and TCM.

Table 4

The Clinical Chemical Drugs and Mechanism for Treatment of Liver Cancer in China.

Drug Name	Mechanism
Chlorogenic acid	Immunostimulants
Dovitinib	Multi-target kinase inhibitor
Sulfonated Monophosphate Mannan Oligosaccharide	PI-88 heparanase inhibitor
Lenvatinib	Multi-target kinase inhibitor
Tyroserleutide	1 Phosphatidylinositol 3 kinase inhibitors; apoptosis stimulants; intercellular adhesion molecule 1 antagonists
p-Toluenesulfonamide	Apoptosis stimulants; cathepsin B modulators; cell death stimulants
Refametinib	Mitogen-activated protein kinase kinase inhibitors
MSC2156119J	c-Met inhibitor
TLC388 HCl	Angiogenesis inhibitors; DNA topoisomerase I inhibitors
Galunisertib	TGF-β receptor type I (TGF-βRI) kinase inhibitor, phosphotransferase inhibitors
Erdafitinib	FGFR Kinase Inhibitor
Miriplatin	DNA cross linking agents; DNA synthesis inhibitors
Brivanib alaninate	Multi-target kinase inhibitor
Chiauranib	Angiogenesis inhibitors; aurora kinase B inhibitors; mitosis inhibitors; vascular endothelial growth factor receptor antagonists
ATG-008	MTORC1 protein inhibitors; MTORC2 protein inhibitors
Hemay102	Not released
Fisogatinib	FGFR4 Inhibitor
Lenvatinib mesylate	Multi-target kinase inhibitor
Mei-ta-fei-ni	Multi-target tyrosine kinase and Raf kinase inhibitor
Detorsertib	mTORC1/mTORC2 inhibitor
DX1002	Tumor angiogenesis inhibitor
ACT001	Combining with plasminogen activator inhibitor-1 (PAI-1) and inhibit the PI3K/AKT pathway

Exclude the commercialized drugs as indications.

The VEGF signaling pathway is an attractive therapeutic target given the vascular dysplasia seen in liver cancer, and several VEGFR antagonists including ATG-008, brivanib, lenvatinib mesylate and ramucirumab are currently in various phases of clinical testing. In addition, trials are also ongoing for the FGF pathway-targeting fisogatinib, mTORC1/mTORC2 inhibitor detorsertib, multi-target tyrosine kinase and Raf kinase inhibitor Mei-ta-fei-ni, etc.

Immune checkpoint blockers including antibodies targeting PD-1, PD-L1 and cytotoxic T lymphocyte antigen-4 (CTLA-4) can potentially be effective against advanced HCC. The anti-PD-1 antibodies currently in clinical trials for HCC include spartalizumab, AK105, TQB2450, CS1003, etc. Tremelimumab, a fully humanized monoclonal antibody against CTLA-4, binds to CTLA-4 expressed on the surface of activated T lymphocytes, and reverses the immunosuppressive state.

Icaritin soft capsules, basil capsules, ginsenoside H dropping pills and Kanglong capsules are the traditional Chinese medicines undergoing clinical testing for liver cancer. A multicenter, randomized open Phase III clinical trial is ongoing to compare the efficacy and safety of sorafenib and icaritin soft capsules for the first-line treatment of patients with PD-L1 positive advanced HCC. In addition, the efficacy and safety of resibufogenin as a first-line treatment for advanced HCC is also being tested in a multicenter, randomized, double-blind, double-simulation phase III clinical trial. It is suggested that some TCM may have the same therapeutic effect as molecular targeted drugs in the treatment of HCC.

Discussion

Liver diseases, in particular hepatitis B, hepatitis C and liver cancer, are associated with considerable morbidity and mortality. An increasing number of clinical trials are registered each year in China for the treatment of liver diseases. However, generic drugs still account for a relatively large proportion of these studies. For example, there are 30 ongoing clinical trials for tenofovir disoproxil fumarate tablets, and the number increases to 37 (5% of all clinical trials on liver diseases) when considering the different dosage forms. In recent years, the “National Innovation-Driven Development Strategy Outline”, “13th Five-Year” National Science and Technology Innovation Plan, and “Pharmaceutical Industry Development Planning Guide” have set up the “Major New Drug Development” program to promote the development of new drugs, which has significantly increased the number of clinical trials of liver-specific innovative drugs.

Nucleotide analogs are still the most popular anti-hepatitis B drugs, although novel agents with greater bioavailability and lower risk of resistance are currently under development. For instance, immunotherapy is a highly promising option for hepatitis B treatment. IFNs also have a long-lasting therapeutic effect and a high clearance rate of viral surface antigens. However, their response rate is low and side effects are significant. Therefore, combination therapies are being considered as a viable alternative.23 The current cocktail therapies under clinical development include nucleotide analogs with/out immunomodulatory drugs. The combination of different analogs can compensate for the limitations of a single drug, although it is not clear whether it can inhibit the latent cccDNA inside liver. Therefore, drugs that directly target cccDNA are the focus of future R&D, along with development of effective delivery systems and minimizing off-target effects of sequence-targeted nucleases.

An effective vaccine is necessary for prevention of CHC, since it frequently progresses to cirrhosis and liver cancer, and the causative HCV is highly mutagenic. IFN combined with ribavirin (RBV) is no longer the standard recommended treatment for CHC due to the low sustained virological response (SVR) or complete cure rate, and the obvious adverse reactions and toxicity.24 So, In the absence of a vaccine, however, DAAs are promising therapeutic agents against hepatis C, but may develop drug resistance after long-term use. Therefore, several clinical trials are testing the compound preparations of two or more DAAs, such as ABT-450/ritonavir/ABT-267 film-coated tablet and Ledipasvir/Sofosbuvir tablet, which can significantly increase the SVR to more than 95%.25,26

Primary liver cancer ranks sixth in terms of incidence, and is the fourth most common cause of cancer-related mortality worldwide.5 It is a highly malignant disease characterized by a high degree of invasiveness and metastasis, and most patients are diagnosed at the advanced stage of cancer. The conventional therapies for primary liver cancer include surgical resection, liver transplantation or local ablation, and transcatheter arterial chemoembolization. Nevertheless, the clinical outcome and prognosis of patients with advanced liver cancer are very poor. Furthermore, the low tolerance of primary liver cancer patients to sorafenib and the emergence of drug resistance stresses the need to develop novel targeted drugs with greater therapeutic efficacy and fewer side effects. The clinical trials of targeted therapy drugs mainly include anti-angiogenesis agents, hepatocyte growth factor inhibitors, mammalian target rapamycin inhibitors, etc. In addition, immunotherapy is currently one of the most promising biological strategies for treating aggressive cancers, and can significantly prolong patient survival.

TCM formulations and compounds are also promising alternatives for treating liver diseases. Ginsenoside H, and its major bioactive component 20 (S)-ginsenoside Rh2, strongly inhibit the growth of cancer cells. It can increase autophagy of HepG2 and Huh7 cells, inhibit β-catenin signaling, regulate immune response and down regulate VEGF, which eventually inhibit cellular growth and migration.27,28 Icaritin, a natural isopentene flavonoid also known as 3,5,7-trihydroxy-2-(4-hydroxymethylphenyl)-8-(3-methylbutenyl-2)–1,2-benzopyranone-4, is the bioactive compound of Epimedium. It inhibits tumor cell proliferation and induces apoptosis by targeting the IL-6/STAT3, IGF1/STAT3 and MAPK/ERK signaling pathways.29,30 In addition, icaritin also induces the differentiation of immunosuppressive cells and thus exerts an immunomodulatory effect.31 The total glycosides of Rhizoma coptidis can significantly inhibit the replication of HBV cccDNA in cells, and thus targets an earlier stage compared to adefovir dipivoxil. Although all of the above drugs are in clinical trials, the complexity of traditional Chinese medicine formulations makes it challenging to develop novel drugs.

This study has some limitations that ought to be addressed. First, although clinical trial platform registration is mandatory as per NMPA regulations, we may have missed some clinical trials that were started prior to the implementation of new policy (before 2013). Nevertheless, we observed a significant spike in the number of clinical trials registered post 2013 due to supplementary registration. Secondly, the statistical analysis was conducted on the basis of the compounds, and the different dosage forms and clinical trials of the same drug were merged as a single candidate. Moreover, innovative drugs only analyze chemical drugs and biological products, while TCM/natural drugs are not analyzed due to their particularity. Thirdly, there is a certain discrepancy between the date of first announcement on the platform and the actual initiation of the clinical trial. We considered the former for the statistical analysis. Fourth, for statistics of major clinical research institutions, the statistically ranked first unit when there are multiple units.

Conclusion

Liver diseases include hepatitis, liver cirrhosis, liver cancer, etc. There is currently no effective treatment strategy that can simultaneously reduce liver injury and necrosis, and promote liver cell regeneration. Therefore, biotech companies and research institutes worldwide have invested heavily in drug R&D for liver diseases. Based on our analysis, we infer stronger macro-control is required for the clinical trials conducted in China. For instance, proper policies and incentives should be formulated, and the development of innovative drugs should be encouraged. The current research foci in China are novel targets for hepatitis B, hepatitis C and liver cancer, preventive hepatitis C vaccine, and targeted therapeutic drugs, TCM/natural drugs and immunotherapeutic drugs for liver cancer.