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Analysis of Next Generation PET and Liquid Biopsy to Monitor mCRPC Treated with Abiraterone: ANGELA trial

Analysis of Next Generation PET and Liquid Biopsy to Monitor mCRPC Treated with Abiraterone: ANGELA trial

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034708
Enrollment
Unknown
Registered
2020-07-15
Start date
2020-07-15
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

Prostate Caner

Interventions

Sponsors

Fudan University Shanghai Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed as mCRPC according to EAU-ESTRO-SIOG 2016 and PSA > 10ng/ml; 2. No previous treatment with novel hormonal therapy; 3. ECOG 0-2; 4. Normal organ function, WBC >= 3000/mm3 or Neutrophil >= 1500/mm3; 5. Aged 18 to 85 years old when issuing written informed consent; 6. Life expectancy > 12 months. 7. Consent and able to carry out follow-up visit and cooperate with all other study procedures.

Exclusion criteria

Exclusion criteria: 1. Severe disease or other medical conditions suggesting a high risk of death within 1 year, which may interfere with follow-up. Decided by investigator; 2. Diagnosed with any other malignant tumor within 3 years before enrollment; 3. Unable to provide necessary follow-up information; 4. Other conditions that are judged as ineligible by the investigator.

Design outcomes

Primary

MeasureTime frame
lesion heterogeneity on dual-tracer PET/CT;genomic change;

Countries

China

Contacts

Public ContactDingwei Ye, Yao Zhu

Fudan University Shanghai Cancer Center

dwyeli_uro@163.com+86 021 64175590

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026