Phase I Study of HSK46575 in Patients With Metastatic Castration-Resistant Prostate Cancer

This is a phase I, open-label, dose-escalation and expansion study to evaluate the safety, tolerability, PK（pharmacokinetics） and PD（pharmacodynamics） of HSK46575 when given orally in patients with metastatic castration-resistant prostate cancer.

Trial Details

NCT ID

NCT07007910

Phase

PHASE1

Sponsor

Haisco Pharmaceutical Group Co., Ltd.

Status

RECRUITING

Cancer Type

Castration-Resistant (CRPC) Prostate Cancer

Interventions

HSK46575

Locations (sample)

Chengdu, Sichuan, China|30.66667,104.06667

Key Eligibility Criteria

Male, aged ≥18 years;
ECOG (Eastern Cooperative Oncology Group) 0-1, expected survival of ≥ 3 months;
Histology or cytology confirmed adenocarcinoma of the prostate;
Radiological evidence of metastatic bone or soft tissue lesions;

For full eligibility, visit ClinicalTrials.gov.

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