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Phase II clinical study of Utidelone UTD1 in metastatic castration-resistant prostate cancer (mCRPC) after standard treatment failure

Phase II clinical study of Utidelone UTD1 in metastatic castration-resistant prostate cancer (mCRPC) after standard treatment failure

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058568
Enrollment
Unknown
Registered
2022-04-11
Start date
2022-04-06
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

prostatic cancer

Interventions

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients voluntarily joined the study and signed the informed consent. 2. Aged >=18 and =3 months.

Exclusion criteria

Exclusion criteria: 1. Had received epomycin within 1 year before administration of the study drug. 2. Severe allergic to epomycin. 3. Patients with grade 3 or above peripheral neurotoxicity during previous chemotherapy. 4. Currently receiving other anti-tumor therapy. 5. Clinically significant mental or central nervous system disorders. 6. Brain metastases with clinical symptoms. 7. Major surgery, or radiotherapy, within 28 days prior to study initiation, or elective surgery required during the study period. 8. Received Chinese herbal or proprietary medicine treatment within 7 days prior to the start of study treatment.

Design outcomes

Primary

MeasureTime frame
PSA remission rate;

Countries

China

Contacts

Public ContactShi Yanxia

Sun Yat-sen University Cancer Center

shiyx@sysucc.org.cn+86 13609058827

Outcome results

None listed

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