TrialSignal
Clinical trial intelligence report
An Open-label, Multicenter Phase Ib/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Anti-tumor Activity of QLC5508 and/or QLH12016 in Combination With Other Anti-tumor Therapies in Subjects With Advanced Prostate Cancer
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 13, 2026
NCT ID
NCT07198633
Status
RECRUITING
Phase
Phase 1/2
Sponsor
Qilu Pharmaceutical Co., Ltd.
Executive brief
Investment-Ready Snapshot
QLC5508 and QLH12016 are being evaluated in combination with established therapies (abiraterone and enzalutamide) for advanced prostate cancer, a significant market with unmet needs. The trial's dual-phase design allows for both safety and efficacy exploration, potentially positioning Qilu Pharmaceutical Co., Ltd. favorably against competitors in the prostate cancer treatment landscape. The study's focus on patients who have failed standard therapies may enhance the asset's appeal in a crowded market. Successful outcomes could lead to accelerated development timelines and increased investor interest, particularly given the rising prevalence of prostate cancer globally.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07198633
Indication
Advanced Prostate Cancer
Modality
small molecule
Target
B7H3 (CD276) - a target for antibody-drug conjugates (ADCs) and PROTACs in advanced prostate cancer.
Intervention
QLC5508, abiraterone acetate, enzalutamide, QLH12016
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.