Umar Saeed ^1* ZAHRA ZAHID PIRACHA ² Muhammad Nouman Tariq ² Shayan Syed ² Muhammad Raza ² Rakshana Munusamy ² Naveen J Bose ² Hassan Abdal ² Saim Munir ² Dilber Uzun Ozsahin ³ İlker Özşahin ⁴ Surya Nauli ^5*

• ¹ Ajou University, Suweon, Republic of Korea
• ² International Center of Medical Sciences Research (ICMSR), Islamabad, Islamabad, Pakistan
• ³ University of Sharjah, Sharjah, United Arab Emirates
• ⁴ Near East University, Nicosia, Cyprus
• ⁵ Chapman University, Orange, California, United States

Chronic Hepatitis B Virus (HBV) infection remains a formidable global health challenge, driving severe liver complications such as hepatocellular carcinoma (HCC) and pyogenic liver abscesses (PLA). At the core of HBV persistence lies covalently closed circular DNA (cccDNA), a viral reservoir that fuels ongoing infection despite antiviral treatments. This review delves into the molecular mechanisms governing cccDNA formation, maintenance, and clearance, spotlighting innovative therapeutic strategies to disrupt this key viral element. We explore cutting-edge approaches, including epigenetic modulation to silence cccDNA, RNA interference (RNAi) for viral RNA degradation, and CRISPR/Cas genome editing to excise cccDNA directly. Additionally, emerging antiviral therapies and immunotherapies, such as therapeutic vaccines and immune checkpoint inhibitors, offer new avenues for enhanced treatment efficacy. Special attention is given to the clinical complexities of managing HBV in patients with co-morbid conditions like HCC and PLA, underscoring the need for personalized treatment regimens. This review advocates for a shift toward precision medicine, highlighting the critical need for interdisciplinary collaboration to bridge molecular discoveries with clinical innovations. Ultimately, these advancements promise to revolutionize the management of chronic HBV, paving the way for potential cures and improved patient outcomes.