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tenofovir disoproxil orotate (Virreal)

✓ Approved

Dong-A ST · · 小分子

什么是 tenofovir disoproxil orotate?

tenofovir disoproxil orotate 是一种小分子,由Dong-A ST研发。该药已获批,用于治疗相关适应症,给药途径:Oral (PO)。

药物档案

商品名Virreal
公司Dong-A ST
药物类别小分子
分子靶点,
给药途径Oral (PO)
状态Approved

作用机制

分子靶点

tenofovir disoproxil orotate 作用于 2 个分子靶点:

gag-pol, HIV-1 (gag-pol)
(P)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

tenofovir disoproxil orotate 针对 2 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Infections and infestationsAcquired immunodeficiency syndrome✓ Approved
Infections and infestationsHepatitis B✓ Approved

相关研究文献

PubMedDiseases (Basel, Switzerland)2026-10-26

Assessing Renal Outcomes After Switching from Tenofovir Disoproxil Fumarate to Tenofovir Alafenamide in People with HIV: Proteinuria Changes and Limits of Causal Attribution.

D'Anna Tommaso T, Trizzino Marcello M, Belmonte Beatrice B, Gioè Claudia C et al.

Background: The total urinary protein-to-creatinine ratio (PCr) measures proteinuria but does not establish tubular injury or its recovery. Methods: We examined PCr changes after switching from tenofovir disoproxil fumarate (TDF) to tenofovir alafenamide (TAF) in a single-centre retrospective cohort of 364 adults with human immunodeficiency virus (HIV) infection. Paired PCr values were available for 159 patients (43.7%). The primary descriptive endpoint was a PCr reduction below 20%, an operational, nonvalidated threshold. Analyses comprised paired rank-based comparisons, baseline-adjusted regression, threshold and influence sensitivity analyses, and nested cross-validation of ridge logistic regression using three predictor sets. Results: The median paired PCr change was -4.0 mg/g (interquartile range -41.5 to 11.5; signed-rank Benjamini-Hochberg-adjusted q = 0.0098); 99/159 patients (62.3%) had a reduction below 20%. Baseline log(1 + PCr) was positively associated with post-switch log(1 + PCr), while its coefficient in the corresponding change model was exactly one unit lower, illustrating mathematical coupling. The cross-validated area under the curve was 0.709 for baseline PCr alone, 0.475 for the other covariates, and 0.701 for all predictors. Conclusions: PCr changes were heterogeneous, and additional covariates did not improve discrimination over the baseline PCr alone. Missing outcomes, unavailable specimen dates, the absence of tubular-specific biomarkers and the uncontrolled design preclude conclusions about irreversible tubular injury, causal treatment effects or clinical prediction utility.

PMID 42929980
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PubMedJournal of the International AIDS Society2026-10-26

Impact of HIV Pre-Exposure Prophylaxis on HIV Incidence and Hepatitis B Outcomes Among Sex Workers Living With Hepatitis B: A Modelling Analysis in Côte D'Ivoire.

Mohareb Amir M AM, Kim Arthur Y AY, Kouamé Menan Gérard MG, Nouaman Marcellin M et al.

Nearly 10% of sex workers in sub-Saharan Africa live with chronic hepatitis B virus (HBV). HIV pre-exposure prophylaxis (PrEP) using tenofovir/emtricitabine (TDF/FTC) has not been studied in this population, possibly due to concerns of hepatitis flares following TDF/FTC cessation. Using a microsimulation model of HIV and HBV disease and data from 2016 to 2024, we compared the clinical impact of TDF/FTC as PrEP versus no TDF/FTC among women who sell sex with HBV in Côte d'Ivoire. We incorporated the anti-HBV effects of TDF/FTC and the increased probability of hepatitis flares and HBV surface antigen (HBsAg) loss following TDF/FTC cessation. We estimated input parameters from published literature: HIV incidence (1.9-3.0 per 100 person-years), PrEP adherence (55%), disengagement from PrEP care (4% per month for the first 12 months, then 12.5% per month), hepatitis flare incidence (2.0-4.0 per 100 person-years) and rate of HBsAg loss (1.0 per 100 person-years), which both increase following TDF/FTC cessation. Model outcomes included cumulative HIV incidence, average hepatitis flares, HBsAg loss and survival over 2, 5 and 10 years. We conducted sensitivity analyses varying HIV incidence, PrEP adherence, disengagement from PrEP care and hepatitis flare rate. Compared with no TDF/FTC, TDF/FTC would reduce cumulative HIV incidence: 4.1% versus 5.6% at 2 years and 10.1% versus 12.7% at 5 years. TDF/FTC would result in more hepatitis flares (mean 0.76 vs. 0.19 per person) and more HBsAg loss (8.4% vs. 5.7%) than no TDF/FTC after 5 years. Two- and five-year survival would be similar between the two strategies, and TDF/FTC would improve survival over longer horizons. Improving adherence and reducing disengagement from care would increase clinical benefits. Even with high disengagement from care and high risk of hepatitis flares, TDF/FTC would reduce HIV acquisition and improve overall long-term survival. Women who sell sex with HBV in Côte d'Ivoire would benefit from TDF/FTC as PrEP to avoid HIV acquisition. The increased risk of hepatitis flares, while challenging to manage in resource-limited settings, would be outweighed by the benefits of HIV prevention. Efforts should be made to scale up PrEP in sex workers, including women with chronic HBV.

PMID 42929139
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PubMedJournal of viral hepatitis2026-10-25

Renal Safety and Antiviral Effectiveness of Tenofovir Alafenamide Versus Entecavir in Patients With Chronic Hepatitis B and Chronic Kidney Disease: A Real-World Cohort Study.

Ren Danfeng D, Dang Xiangyun X, Fu Shan S, Zhang Ze Z et al.

Real-world data on tenofovir alafenamide (TAF), especially in patients with advanced renal impairment, are scarce. We evaluated its renal safety and antiviral effectiveness versus entecavir (ETV) in patients with chronic hepatitis B (CHB) and pre-existing chronic kidney disease (CKD). In this retrospective single-centre study, CHB patients with pre-existing CKD treated with TAF or ETV were included. The primary outcome was change in estimated glomerular filtration rate (eGFR) over 48 weeks. Secondary outcomes included virological, biochemical and metabolic responses. Exploratory subgroup analyses were performed by CKD stage and dialysis status. Among 54 patients (35 TAF, 19 ETV), renal function remained stable in both groups. eGFR change from baseline to week 48 was not significantly different between the TAF and ETV groups (1.56 ± 8.14 vs. -0.53 ± 9.78 mL/min/1.73 m2; Δchange, 2.09; 95% CI, -0.35 to 7.68; p = 0.46). Both groups achieved sustained viral suppression, with no significant difference in undetectable HBV DNA in week-48. HBsAg reduction was greater with TAF than with ETV (-0.36 ± 0.42 vs. 0.02 ± 0.34 log10 IU/mL; p = 0.01). Exploratory analyses in patients with eGFR < 30 mL/min/1.73 m2, TAF showed effective viral suppression and renal safety regardless of dialysis status. Metabolic parameters remained stable, without complex dose adjustments. TAF was safe and effective in CHB patients with CKD, including those with advanced renal impairment. Its renal safety and antiviral effectiveness did not differ significantly from those of ETV, with the practical advantage of fixed dosing without complex adjustment.

PMID 42922336
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PubMedChemistry & biodiversity2026-10-25

Experimental and Pharmacoinformatic Studies Reveal Allium cepa L. Extract-Mediated Modulation of Hepatitis B Virus Associated Inflammatory Pathways via Quercetin Glucoside Derivatives.

Gujarathi Swarup S SS, R Harish Darasaguppe D, Patil Vishal S VS, Karikazi Adilmehadi A et al.

Hepatitis B virus (HBV) infection remains a major global health burden and often progresses to chronic liver inflammation, fibrosis, and hepatocellular carcinoma. Although current antiviral therapies effectively suppress viral replication, their ability to modulate HBV-associated complications remains limited. This study investigates the HBV-associated antiviral and host modulatory potential of methanolic extract of Allium cepa bulb (AC) using integrated in vitro and computational approaches. Cytotoxicity, reverse transcriptase inhibition, time- and dose-dependent inhibition of HBsAg and HBeAg levels, inflammatory cytokines, and specific host gene expression linked to HBV infections were assessed using HBV-expressing HepG2.2.15 cells. LC-MS detected phytocompounds were evaluated for their interaction with TLR4 using molecular docking and dynamics simulations using the Schrödinger suite. AC treatment reduced HBsAg and HBeAg levels up to 61.0% and 75.37%, respectively. Co-treatment with Tenofovir alafenamide enhanced the inhibition to 79.0% and 94.55% without compromising cell viability. Among LC-MS-identified phytocompounds, computational analysis revealed stable interactions with Quercetin 3,4'-diglucoside exhibiting the highest affinity (-14.23 kcal/mol) and maintaining stability with TLR4 throughout a 100 ns simulation. Overall, AC attenuated HBV-induced inflammation through predicted modulation of TLR4-mediated pathways and reduction of HBV antigen secretion, supporting its potential as a complementary therapeutic candidate for the management of chronic HBV infection.

PMID 42922067
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PubMedThe Journal of infectious diseases2026-10-25

A novel injectable drug-combination nanoparticle containing three antiretrovirals designed for HIV treatment: A first-in-human trial.

Bender Ignacio Rachel A RA, Jonsson Christine C, Perazzolo Simone S, Stephen Zachary Z et al.

Long-acting antiretroviral therapy may improve adherence and decrease stigma, yet affordable combination formulations for global usage are lacking. The TLC-ART program engineered an injectable 3-drug combination in a novel nanoparticle (DcNP) product "TLC-ART 101," composed of lopinavir (LPV), ritonavir (RTV), and tenofovir (TVF) and two lipid excipients. We report safety and pharmacokinetics from this first-in-human study. Three dose cohorts of people without HIV received a single subcutaneous dose of 1.5, 3.0 or 4.0 mL in an adaptive trial of up to64 days. LPV, RTV, and TFV were measured over time in plasma, peripheral blood mononuclear cells (PBMC), and lymph nodes (n=2). All 12 participants completed the study. One participant experienced anaphylaxis, and four had non-serious hypersensitivity events (rash, lip swelling, generalized pruritis). All participants had grade 1-2 injection-site reactions.. At the highest dose, median LPV T1/2 was 17 days, and LPV was detectable through two months in most participants. RTV T1/2 was 12hrs. Plasma TFV T1/2 was 3.5 days; TFV-diphosphate was detected intracellularly through 14 days. Total exposure (AUC) was higher in peripheral blood mononuclear cells versus plasma for all 3 drugs. The first human application of this novel HIV DcNP resulted in detection of LPV through two months and TFV up to four days in plasma, and no meaningful prolongation of RTV. Systemic hypersensitivity was common, and although IgE elevation was not observed, additional mechanistic understanding is required prior to further development of this DcNP pipeline.

PMID 42925035
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PubMedHepatology international2026-10-23

Higher relapse rate after stopping tenofovir alafenamide compared with entecavir; but not tenofovir disoproxil fumarate in HBeAg-positive patients.

Wan Kuan-Hung KH, Peng Cheng-Yuan CY, Kuo Yuan-Hung YH, Hu Tsung-Hui TH et al.

This study compares the hepatitis B virus (HBV) relapse rates after discontinuation of entecavir, tenofovir disoproxil fumarate (TDF), or tenofovir alafenamide (TAF) therapy in HBeAg-positive patients. This study was a retrospective analysis of a prospectively collected cohort comprising 427 HBeAg-positive patients without cirrhosis who received entecavir (n=200), TDF (n=133), or TAF (n=94) were enrolled. All patients met the Taiwan National Health Insurance stopping criteria for antiviral therapy. At 156 weeks, the cumulative incidences of virological relapse and clinical relapse, and retreatment were higher in the off-TAF group (85.3%, 73.7%, and 76.6%, respectively) than in the off-entecavir group (58.0%, 45.5%, and 38.9%, respectively) (all p <0.001). Compared with the off-TDF group (74.6%, 64.4%, and 58.8%, respectively), the off-TAF group showed comparable rates of virological relapse (p=0.139) but significantly higher rates of clinical relapse (p=0.042) and retreatment (p=0.003). The median time to clinical relapse was earlier in patients discontinuing TAF than in those discontinuing entecavir or TDF (17, 42, and 24 weeks, respectively). Multivariable analysis demonstrated that TAF therapy was an independent risk factor for virological relapse, clinical relapse, and retreatment compared with entecavir, but not with TDF; these findings remained consistent after propensity score matching. Among patients with clinical relapse, HBeAg seroreversion was more frequent in the off-TAF group than in the off-entecavir (73.0% vs. 51.4%, p <0.001) and off-TDF groups (73.0% vs. 56.8%, p=0.029). Discontinuation of TAF therapy was associated with earlier and higher HBV relapse rates compared with entecavir, but not TDF, in HBeAg-positive patients.

PMID 42909761
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