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Study to Describe the Treatment Patterns and Associated Clinical Outcomes in Patients With Metastatic Castration-resistant PROstate Cancer

A Multi-country, Multi-centre, Non-interventional, REtrospective Study to Describe the Real-world Treatment Patterns and Associated Clinical Outcomes in Patients With Metastatic Castration-resistant PROstate Cancer - REMPRO Registry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/11/038126
Enrollment
2000
Registered
2021-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: C61- Malignant neoplasm of prostate

Interventions

None listed

Sponsors

AstraZeneca Pharma India Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male patients = 18 years of age OR legal age of being an adult in the country as per local regulations 2. Patient or next of kin/legal representative (for deceased patients at study entry, unless a waiver is granted) willing and able to provide written informed consent according to the local regulations 3. Patients with a diagnosis of metastatic (stage IV) mCRPC, confirmed by either biopsy of a metastatic tumour site, or by history of biopsy-proven localized disease and evidence of metastatic disease on imaging studies (which is clearly noted in hospital/clinical records) and progression on ADT alone between 01 January 2016 and 31 December 2018 4. Availability of medical records at the participating site reflecting at least one LOT received and at least 12 months of follow-up from the index date (unless the patient died/lost to follow-up within the first 12 months after diagnosis)

Exclusion criteria

Exclusion criteria: 1. Patients with a concomitant cancer at the time of diagnosis of mCRPC or those who are treated with any anti-cancer therapy indicated for other cancers within 6 months of diagnosis of mCRPC, except for non-metastatic non-melanoma skin cancers or in situ or benign neoplasms. 2. Patients unable to give an informed consent (unless a waiver is granted)

Design outcomes

Primary

MeasureTime frame
To describe the real-world treatment patterns in patients with mCRPCTimepoint: one time

Secondary

MeasureTime frame
To describe the demographic and clinico-pathological characteristics of patients diagnosed with mCRPC To determine the survival outcomes associated with different treatment regimens used for mCRPC To assess the real-world effectiveness (including real-world progression-free survival [rwPFS] and real-world response rate [rwRR]) of different treatment regimens used for mCRPC To characterize BRCA1/2 and HRRm status in patients with mCRPC, if availableTimepoint: one time

Countries

Argentina, Brazil, Chile, Colombia, Egypt, India, Malaysia, Russian Federation, Saudi Arabia, Taiwan, United Arab Emirates

Contacts

Public ContactMr Amit Kumar

AstraZeneca Pharma India Ltd

archita.joshi@astrazeneca.com

Outcome results

None listed

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