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In addition, fungi enter deep tissues to generate invasive fungal infections (IFIs), a long\u2010term worldwide health risk, especially for HIV\/chemotherapy patients with compromised immune systems. The present treatment uses single\u2010target antifungals like azoles, allylamines, and pyrimidines. But drug\u2010resistant fungi and widespread adverse effects have limited their therapeutic efficacy. Thus, innovative, safe, and effective antifungals are needed. Through the 20th century, the pharmaceutical industry adopted the \u201cone molecule, one target, one disease\u201d mentality which led to various effective selective drugs that will dominate disease treatment. But, unfortunately, even with the best research, targeting one target may not work in complicated illnesses. Thus, drugs that activate several targets simultaneously, to improve efficacy and safety, are gaining interest. Multitarget medicines involve monotherapies, medication cocktails, and combination drugs. The second method, multitarget\u2010directed ligands (MTDLs), uses one active component that treats multifactorial diseases. In MTDL, new chemical entities (NCEs) are created which may solve various issues related to combination therapies, including: (1) establishing balanced and multi\u2010selective potency across targets, (2) matching PK\/PD properties for components, (3) better patient compliance, (4) straightforward approval from regulatory authorities, (5) higher cost of medication etc. To optimize developability, effectiveness, and safety, multitarget drug design should be more methodical and thorough in target combinations, ligand selection, and desired activity equilibrium. In this review, the hybrid, dual\u2010targeting antifungal agents are classified into four major categories, based on the combination of their mechanisms, namely\u2014(\n                    <jats:bold>1<\/jats:bold>\n                    ) Antifungal + antifungal (involves dual mode of DNA damage + membrane polarization), (\n                    <jats:bold>2<\/jats:bold>\n                    ) Antifungal + Resistance reversal (includes proteasome inhibition, Coumarin + CYP51 inhibitors, CYP51\u2009+\u2009Hsp90 inhibitors), (\n                    <jats:bold>3<\/jats:bold>\n                    ) Antifungal + Host immunity modulators (includes CYP51\u2009+\u2009HDAC inhibitors, NLRP3 inflammasome + AHAS inhibitors, COX\u2009+\u2009CYP51 inhibitors, PD\u2010L1\u2009+\u2009CYP51 inhibition etc.), (\n                    <jats:bold>4<\/jats:bold>\n                    ) Azole sensitisers (JAK2\u2009+\u2009HDAC inhibition, BRD4\u2009+\u2009HDAC inhibition etc.), (\n                    <jats:bold>5<\/jats:bold>\n                    ) Multifunctional, miscellaneous antifungal agents (DNA intercalation + intracellular ROS production) etc. Thus, it covers significant achievements and the associated challenges of antifungal multitarget drug design, which might be helpful to the researchers who are interested in delving into the development of fungicidal agents as a drug to address the burning question of drug\u2010resistant\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>Candida albicans<\/jats:italic>\n                    <\/jats:styled-content>\n                    and invasive fungal infections (IFIs).\n                  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