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A non-interventional, multicenter, retrospective real-world study on the treatment of mHSPC by Rilvigliam combined with ADT

A non-interventional, multicenter, retrospective real-world study on the treatment of mHSPC by Rilvigliam combined with ADT

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115647
Enrollment
Unknown
Registered
2025-12-29
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic hormone sensitive prostate cancer

Interventions

ADT+Rezvilutamide:N/A

Sponsors

The First Affiliated Hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years; 2. Diagnosed with mHSPC; 3. Has used ADT and is receiving enzalutamide treatment during the hormone-sensitive phase; 4. Can be combined with docetaxel chemotherapy; 5. Can undergo local treatments such as radiotherapy or surgery; 6. In the mHSPC phase, switched to enzalutamide treatment due to other drug side effects while the tumor has not progressed.

Exclusion criteria

Exclusion criteria: 1. The patient's pathological results suggest neuroendocrine prostate cancer, among others. 2. Patients with no metastases detected on imaging; if there is lymph node metastasis, it is confined to the pelvic lymph nodes. 3. Patients with mCRPC; 4. Use of relugolix due to progression on other second-generation drugs.

Design outcomes

Primary

MeasureTime frame
Prostate-specific antigen;

Secondary

MeasureTime frame
Blood Biochemistry;

Countries

China

Contacts

Public ContactQi Ma

The First Affiliated Hospital of Ningbo University

45112409@qq.com+86 574 8708 9078

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026