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CTRI Number  CTRI/2024/08/072504 [Registered on: 14/08/2024] Trial Registered Prospectively
Last Modified On: 12/08/2024
Post Graduate Thesis  No 
Type of Trial  Observational 
Type of Study   Cohort Study 
Study Design  Other 
Public Title of Study   Scientific data review of prostate cancer patients to study treatment patterns and understand need gaps.  
Scientific Title of Study   Real-World Treatment Patterns and Clinical Outcomes Among Patients with Metastatic Castration-resistant Prostate Cancer (mCRPC): An Emerging Market Medical Record Review Study 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
Protocol C3441067 version 1 dated 15 December 2023  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Antara Chaudhri 
Designation  Medical Advisor 
Affiliation  Pfizer Limited 
Address  The Capital Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East

Mumbai
MAHARASHTRA
400051
India 
Phone  9971012224  
Fax    
Email  Antara.Chaudhri@pfizer.com  
 
Details of Contact Person
Scientific Query
 
Name  Antara Chaudhri 
Designation  Medical Advisor 
Affiliation  Pfizer Limited 
Address  The Capital Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East

Mumbai
MAHARASHTRA
400051
India 
Phone  9971012224  
Fax    
Email  Antara.Chaudhri@pfizer.com  
 
Details of Contact Person
Public Query
 
Name  Antara Chaudhri 
Designation  Medical Advisor 
Affiliation  Pfizer Limited 
Address  The Capital Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East


MAHARASHTRA
400051
India 
Phone  9971012224  
Fax    
Email  Antara.Chaudhri@pfizer.com  
 
Source of Monetary or Material Support  
Pfizer Limited, The Capital Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East, Mumbai, Maharashtra 400051 
 
Primary Sponsor  
Name  Pfizer Limited 
Address  The Capital Plot No. C, The Capital, 1802, 18th Floor, 70, G Block Rd, Bandra Kurla Complex, Bandra East, Mumbai, Maharashtra 400051 
Type of Sponsor  Pharmaceutical industry-Indian 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India
Argentina
Brazil
Saudi Arabia
Taiwan
Turkey
United Arab Emirates  
Sites of Study  
No of Sites = 4  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr J B Sharma  Action Cancer Hospital  Room No FC-34, A - 4, Department of Medical Oncology, Paschim Vihar, New Delhi - 110063, India
New Delhi
DELHI 
9811167505

dr_sharmajb@rediffmail.com 
Dr Srikant Tiwari  Jawaharlal Nehru Cancer Hospital & Research center  Room No- 10, Department of Medical Oncology RP.O. Box No. 32, Jawaharlal Nehru Cancer Hospital & Research center, Cancer Hospital Road, Idgah Hills, Bhopal, Madhya Pradesh - 462001, India
Bhopal
MADHYA PRADESH 
0755-2665720

srikantabhinov@gmail.com 
Dr Sandeep Batra  Max Super Speciality Hospital  Service Floor, 2, Department of Medical Oncology, Press Enclave Road, Saket Institutional Area, Saket, New Delhi, Delhi – 110017, India
New Delhi
DELHI 
9811035061

sandeepriya2000@yahoo.com 
Dr Amit Joshi  Tata Memorial Hospital  Room No - 1105, 11th floor, Tata Memorial Centre, Homi bhabha block, Dr. Ernest Borges Road, Parel, Mumbai - 400012, India
Mumbai
MAHARASHTRA 
9769331525

dramitjoshi74@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 4  
Name of Committee  Approval Status 
Action Cancer Hospital Ethics Committee  Submittted/Under Review 
Instituational Ethics Committee Jawaharlal Nehru Cancer Hospital & Research center  Approved 
Max Healthcare Ethics Committee  Submittted/Under Review 
TMH, Institutional Ethics Committee-I  Submittted/Under Review 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: N428||Other specified disorders of prostate,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  NIL  NIL 
Comparator Agent  NIL  NIL 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  99.00 Year(s)
Gender  Male 
Details  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. 
 
ExclusionCriteria 
Details  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). 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   On-site computer system 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
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 mCRPC 
24 Months 
 
Secondary Outcome  
Outcome  TimePoints 
NA  NA 
 
Target Sample Size   Total Sample Size="950"
Sample Size from India="150" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   30/08/2024 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  11/07/2024 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="2"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Open to Recruitment 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Prostate cancer is the second most common cancer worldwide and the fifth leading cause of cancer-related mortality among men. In 2020, there were 1.4 million new cases of prostate cancer worldwide, accounting for 7.3% of all cancer cases; and 0.4 million deaths, accounting for 3.8% of all cancer-related deaths. Incidence rates (per 100,000 people) vary globally, with the highest rates being reported in Northern Europe (83.4) and Western Europe (77.6), whilst the lowest rates are reported in South Central Asia (6.3), South-East Asia (13.5), and Northern Africa (16.6). Specifically, the incidence rates (per 100,000 people) in Emerging Market (EM) (eg: India: 5.0-9.1, Taiwan: 17.2-52.9, Turkey: 42.5, Saudi Arabia: 7.0, United Arab Emirates [UAE]:13.4, Egypt: 13.9, Argentina: 42.0) were lower than developed countries.

 Mortality rates due to prostate cancer, since mid-1990s, have decreased in most high-income countries, including those in North America, Oceania, and Northern and Western Europe. However, during the same period, increased mortality rates have been observed in Central and Eastern Europe, Asia, and Africa. Around 4%-15% of prostate cancer cases are already metastatic at diagnosis; and approximately 10%-50% of prostate cancer cases progress into mCRPC within 3 years of diagnosis. The long-term prognosis for mCRPC is poor, with an OS since development of castration resistance ranging from 13 to 33 months, which varies depending on individual and disease characteristics, as well as treatment.

Data on mCRPC epidemiology, disease burden, and treatment landscape is scarce across EM compared with the US and other developed markets. The lack of this data is an important barrier to formulating treatment strategies and guidelines. To bridge this gap, it is planned to capture real-world data to yield an enhanced picture of patient characteristics and treatment patterns; these data can uncover areas where current clinical needs are not being met and offer insights into how innovative therapies can enhance patient outcomes. This study therefore seeks to describe demographic and clinical characteristics, treatment patterns, clinical outcomes, and healthcare resource use (HCRU) where applicable among patients with mCRPC in EM.

 By means of study we would hereby like to notify your Directorate about conduct of non-interventional study- ‘Real-World Treatment Patterns and Clinical Outcomes Among Patients with Metastatic Castration-resistant Prostate Cancer (mCRPC): An Emerging Market Medical Record Review Study’. Protocol Number C3441067, Version 1.0 Dated 15 December 2023.’

 
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