ACA is a botanical drug candidate developed to reduce pain and skin reactions associated with radiotherapy. Having completed a Phase I clinical trial, ACA demonstrates potential to improve treatment tolerance and quality of life for cancer patients undergoing radiation therapy.
Radiotherapy is a cornerstone of cancer treatment, yet over 95% of patients experience radiation-induced dermatitis (RID), with 10–25% developing moderate to severe skin reactions that may impact treatment adherence and quality of life.
Current treatment options remain limited, highlighting a significant unmet need for therapies that reduce inflammation, protect skin integrity, and support tissue repair.
Market Opportunity
*20 Million+ New Cancer Cases Annually
*7.5 Million+ Patients Receive Radiotherapy Each Year
*95%+ Experience Radiation-Induced Dermatitis
*10–25% Develop Moderate to Severe Skin Reactions
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2.2.Behroozian, T., Goldshtein, D., Wolf, J. R., van den Hurk, C., Finkelstein, S., Lam, H., Patel, P., Kanee, L., Lee, S. F., Chan, A. W., Wong, H. C. Y., Caini, S., Mahal, S., Kennedy, S., Chow, E., & Bonomo, P. (2023). MASCC clinical practice guidelines for the prevention and management of acute radiation dermatitis: Part 1) systematic review. eClinicalMedicine, 58, Article 101886.
3.3.Cheng, J., Dong, J., Fang, Y., Zhang, X., & Dang, X. (2026). Radiation-induced skin injury: A review of pathophysiology, assessment, management, and re-irradiation protocols. Frontiers in Oncology, 15, Article 1736717.