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Clinical trial intelligence report
A Phase Ib Study to Explore the Safety, Tolerability, and Pharmacokinetics of HS-20093 Combination With HRS-5041 in Patients With Advanced Prostate Cancer
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 20, 2026
NCT ID
NCT07115446
Status
RECRUITING
Phase
Phase 1b
Sponsor
Hansoh BioMedical R&D Company
Executive brief
Investment-Ready Snapshot
HS-20093, a fully humanized IgG1 antibody-drug conjugate targeting B7-H3, is being evaluated in combination with HRS-5041, a PROTAC targeting androgen receptors, for the treatment of advanced prostate cancer. The market for prostate cancer therapeutics is significant, with increasing demand for innovative treatments, particularly for metastatic castration-resistant prostate cancer (mCRPC). The combination approach may provide a competitive edge against existing therapies by targeting multiple pathways involved in tumor progression. Given the current landscape, successful outcomes could position Hansoh BioMedical favorably in the oncology market, potentially leading to partnerships or licensing opportunities. Diligence should focus on the safety profile and efficacy data as they emerge, particularly in relation to existing therapies targeting similar pathways.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07115446
Indication
Advanced Prostate Cancer
Modality
small molecule
Target
B7-H3 (CD276) and androgen receptors
Intervention
HS-20093, HRS-5041
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.