Condition: Advanced Prostate Cancer

Study Type: Interventional

Clinical Trials Identifier NCT 8-digits: NCT07115446

Sponsor: Hansoh BioMedical R&D Company

Phase: Phase 1

Eligibility:

• Age: minimum 18 Years maximum N/A
• Gender: Male

Inclusion Criteria:

• Men greater than or equal to 18 years.
• Voluntarily to participate, Signed and dated Informed Consent Form.
• Patients with metastatic castration-resistant prostate cancer (mCRPC) who progressed after at least one type of novel hormonal therapy (standard treatment).
• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0~1.
• Estimated life expectancy ≥ 12 weeks.
• Men should use adequate contraceptive measures throughout the study, up to 3 months after the last dose of HRS-5041 or 4.5 months after the last dose of HS-20093 (whichever is later).

Exclusion Criteria:

• Treatment with any of the following: a. Previous or current treatment with B7-H3 targeted therapy. b. Previous treatment with AR PROTAC. c. Any cytotoxic chemotherapy, investigational agents and anticancer drugs within 21 days prior to the first scheduled dose of HS-20093+HRS-5041. d. brain metastases.
• Any unresolved toxicities from prior therapy greater than Grade 2 according to Common Terminology Criteria for Adverse Events (CTCAE) 5.0.
• History of other primary malignancies.
• Inadequate bone marrow reserve or organ dysfunction.
• Severe, uncontrolled or active cardiovascular diseases.
• Severe or uncontrolled diabetes.
• The presence of active infectious diseases.
• Any known or suspected interstitial lung disease.
• History of serious neuropathy or mental disorders.
• History of severe hypersensitivity reaction, severe infusion reaction.
• Hypersensitivity to any ingredient of HS-20093.
• Unlikely to comply with study procedures, restrictions, and requirements in the opinion of the investigator.
• Any disease or condition that, in the opinion of the investigator, would compromise subject safety or interfere with study assessments.

View trial on ClinicalTrials.gov