A Phase 2 Study of HW211026 in Participants With Actinic Keratosis

Key Inclusion Criteria: * Aged ≥ 18 years, male or female. * At least 2 clinically typical target actinic keratosis lesions on the face. * Willing to avoid direct sun or ultraviolet exposure to the treatment area during the trial. * Fully informed about the study, voluntarily sign the informed consent form, and be able to comply with study procedures and follow-up examination requirements. Key Exclusion Criteria: * Clinically atypical and/or rapidly changing actinic keratosis lesions, such as hypertrophic lesions, hyperkeratotic lesions, and/or cutaneous horns. * Presence of incompletely healed wounds or suspected squamous cell carcinoma, basal cell carcinoma, or other malignant tumors within 5 cm of the actinic keratosis lesions. * Participants with other skin diseases or skin conditions that, in the investigator's judgment, may interfere with the evaluation of safety or efficacy. * Participants who are unable to discontinue immunomodulators, immunosuppressants, cytotoxic agents, or corticosteroids from 1 month prior to signing the informed consent form until study completion or early withdrawal. * Participants who have undergone major surgery within 3 months prior to screening, or who plan to undergo surgery during the trial, as determined by the investigator. * Participants who have participated in any investigational drug clinical trial and received an investigational product within 3 months prior to screening.