The airborne fungus
Aspergillus fumigatus
poses a serious health threat to humans by causing numerous invasive infections and a notable mortality in humans, especially in immunocompromised patients. Mould-active azoles are the frontline therapeutics employed to treat aspergillosis. The global emergence of azole-resistant
A
.
fumigatus
isolates in clinic and environment, however, notoriously limits the therapeutic options of mould-active antifungals and potentially can be attributed to a mortality rate reaching up to 100 %. Although specific mutations in
CYP
51A
are the main cause of azole resistance, there is a new wave of azole-resistant isolates with wild-type
CYP
51A
genotype challenging the efficacy of the current diagnostic tools. Therefore, applications of whole-genome sequencing are increasingly gaining popularity to overcome such challenges. Prominent echinocandin tolerance, as well as liver and kidney toxicity posed by amphotericin B, necessitate a continuous quest for novel antifungal drugs to combat emerging azole-resistant
A
.
fumigatus
isolates. Animal models and the tools used for genetic engineering require further refinement to facilitate a better understanding about the resistance mechanisms, virulence, and immune reactions orchestrated against
A
.
fumigatus
. This review paper comprehensively discusses the current clinical challenges caused by
A
.
fumigatus
and provides insights on how to address them.