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Scientific data review of prostate cancer patients to study treatment patterns and understand need gaps.

Real-World Treatment Patterns and Clinical Outcomes Among Patients with Metastatic Castration-resistant Prostate Cancer (mCRPC): An Emerging Market Medical Record Review Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/08/072504
Enrollment
950
Registered
2024-08-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: N428- Other specified disorders of prostate

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL Control Intervention2: NIL: NIL

Sponsors

Pfizer Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. New diagnosis of mCRPC during the case selection window (between 15 April 2019 to 14 January 2022, inclusive). mCRPC is defined as the current and/or historical presence of metastases on any imaging modality with evidence of disease progression (a rising PSA or radiographic progression (as defined by the investigator) despite ongoing castration therapy [LHRH agonist / antagonist or prior surgical orchiectomy]). 2. Aged at least 18 years upon diagnosis of mCRPC. Of note, patients may be alive or deceased at the date of data abstraction.

Exclusion criteria

Exclusion criteria: Previously enrolled in an interventional trial related to CRPC (patients may have been enrolled in trials of primary treatment and/or hormone-sensitive prostate cancer).

Design outcomes

Primary

MeasureTime frame
Describe demographic and clinical characteristics at first diagnosis of mCRPC. Document treatment patterns from original prostate cancer diagnosis leading up to, upon and following diagnosis of mCRPC. Assess clinical outcomes among patients diagnosed with mCRPC, including prostate-specific antigen (PSA) response, real-world progression-free survival (PFS), real-world objective response rate (ORR), OS, and death by treatment lines. Report mCRPC-specific HCRU where applicable Document time on treatment for each line of treatment for mCRPC Document time to next treatment from initiation of a systemic therapy line to the commencement of the subsequent systemic therapy line for mCRPC Document time to subsequent chemotherapy from initiation of first-line systemic treatment for mCRPCTimepoint: 24 Months

Secondary

MeasureTime frame
NATimepoint: NA

Countries

Argentina, Brazil, India, Saudi Arabia, Taiwan, Turkey, United Arab Emirates

Contacts

Public ContactAntara Chaudhri

Pfizer Limited

Antara.Chaudhri@pfizer.com9971012224

Outcome results

None listed

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