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

NCT ID: NCT07007910

Last Updated: 2025-06-06

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-12-18
• Study Completion Date: 2026-12-31

Brief Summary

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.

Detailed Description

The study will contain two phases: Phase Ia is dose escalation phase and Phase Ib is dose expansion phase.

Phase Ia will contain two part: Dose Escalation Part and Extension Part. Dose Escalation Part based on the "3+3" design for dose escalation and safety evaluation requirements. Patient cohorts at selected doses may be extended to further investigate the tolerability, PK and PD of HSK46575. The number of patients to be enrolled will be up to 10 subjects in each Extension Part cohort. Approximately 30 subjects will be enrolled in Phase Ia.

Phase Ib no less than 60 subjects will be enrolled in each expansion cohort.

Conditions

m CRPC

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Phase Ia (Dose Escalation Part): HSK46575

Phase 1a (Dose Escalation Part): dose escalation of HSK46575 at various dose levels

Group Type: EXPERIMENTAL

HSK46575

Intervention Type: DRUG

co-administered with glucocorticoid and fludrocortisone, orally daily

Phase Ia (Extension Part): HSK46575

Phase 1a (Part B): dose extention of HSK46575 at certain dose levels

Group Type: EXPERIMENTAL

HSK46575

Intervention Type: DRUG

co-administered with glucocorticoid and fludrocortisone, orally daily

Phase Ib: HSK46575

Phase 1b: dose expansion for HSK46575 at dose of RP2D（Recommended Phase II Dose）

Group Type: EXPERIMENTAL

HSK46575

Intervention Type: DRUG

co-administered with glucocorticoid and fludrocortisone, orally daily

Interventions

HSK46575

co-administered with glucocorticoid and fludrocortisone, orally daily

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male, aged ≥18 years;

2. ECOG (Eastern Cooperative Oncology Group) 0-1, expected survival of ≥ 3 months;

3. Histology or cytology confirmed adenocarcinoma of the prostate;

4. Radiological evidence of metastatic bone or soft tissue lesions;

5. Ongoing medical castration or previous surgical castration;

6. Testosterone at castration level during screening;

7. Prior to screening, subjects with evidence of disease progression while receiving ADT (androgen deprivation therapy);

8. Had progressed on at least one novel endocrine therapy, and had progressed on at least one taxane-based chemotherapy (or those who are intolerant or refuse chemotherapy);

9. The functional level of organs must meet the requirements.

Exclusion Criteria

1. Subjects with known hypersensitivity to the active ingredient or excipients of HSK46575 Tablets;

2. Subjects who have received any antitumor therapy within 4 weeks (or 5 half-lives, whichever is shorter) prior to the first dose; or treatment with nitrosoureas, bicalutamide, or nilutamide within 6 weeks (or 5 half-lives, whichever is shorter) prior to the first dose;

3. Subjects whose toxicity from prior anticancer therapy remains > Grade 1 before the first dose;

4. Subjects who have used strong or moderate CYP3A4 inhibitors or inducers, CYP2C9 sensitive substrates, and OCT2 or MATE1 substrates within 14 days or 5 half-lives prior to the first dose of the investigational drug, whichever is longer;

5. Subjects who have undergone Grade 3-4 surgery;

6. Subjects who plan to receive any other antitumor therapy during the study ;

7. Subjects with active metastases to central nervous system;

8. Subjects with serious bone damage caused by prostate cancer bone metastasis as assessed by the investigators;

9. Within 6 months before the first dose, subjects had concurrent pituitary or adrenal dysfunction;

10. Subjects with uncontrolled hypertension;

11. Subjects with central nervous system disorders such as epilepsy and multiple sclerosis;

12. Subjects with active cardiac disease within 6 months prior to the first dose, or a history of arterial or venous thromboembolism;

13. Subjects with a QTc interval prolongation to >470 ms during the screening period calculated by the Fridericia formulaï¼›

14. Subjects with a history of other malignancies;

15. Subjects with a history of immunodeficiency;

16. Subjects with active HBV, HCV, or syphilis infection;

17. Subjects who have participated in other clinical studies within 4 weeks before the first dose;

18. Other conditions.

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Haisco Pharmaceutical Group Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

West China Hospital of Sichuan University

Chengdu, Sichuan, China

Site Status: RECRUITING

Countries

China

Central Contacts

Yunfen Li

Role: CONTACT

liyunfen@haisco.com

18108214952

Facility Contacts

Ping Feng

Role: primary

617130961@qq.com

15388216625

Qiang Wei

Role: backup

wq933@hotmail.com

18980601425

Other Identifiers

HSK46575-101

Identifier Type: -

Identifier Source: org_study_id