Acalabrutinib (ACP-196): Your Essential Guide to This Potent BTK Inhibitor

Explore the groundbreaking potential of Acalabrutinib (ACP-196), a leading second-generation Bruton's tyrosine kinase (BTK) inhibitor, revolutionizing cancer therapy with its enhanced selectivity and efficacy.

Get a Quote & Sample

Key Advantages of Acalabrutinib

Enhanced Selectivity

Acalabrutinib exhibits superior target specificity, demonstrating significantly higher selectivity for BTK over other TEC kinase family members, which contributes to its favorable safety profile and reduces off-target effects, a critical factor in cancer therapy.

Potent Efficacy in B-cell Malignancies

As a leading BTK inhibitor for CLL, Acalabrutinib has proven effective in treating various B-cell malignancies, offering a vital therapeutic option for patients with limited treatment choices and improving overall survival rates.

Improved Safety Profile

Compared to its predecessors, Acalabrutinib offers a more favorable safety profile, with fewer cardiovascular toxicities and a reduced rate of treatment discontinuation due to adverse events, making it a preferred choice in cancer therapy.

Key Applications

Cancer Treatment

Acalabrutinib is a crucial pharmaceutical intermediate used in the development of targeted cancer therapies, particularly for B-cell malignancies, offering new hope for patients.

Pharmaceutical Intermediate

Its role as a pharmaceutical intermediate is vital in drug discovery and development, supporting the creation of advanced treatments within the pharmaceutical API development sector.

Precision Medicine

Acalabrutinib exemplifies precision medicine in oncology, tailoring treatment to individual patient profiles and disease characteristics for optimal therapeutic outcomes.

BTK Inhibitor Research

The compound is instrumental in BTK inhibitor research, enabling further understanding of targeted therapies and paving the way for next-generation treatments in hematological cancers.