Biobanking for Cancer

(PMT Trial)

Not currently recruiting at 15 trial locations
RF
TR
KT
SM
Overseen BySuzan McNamara, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Sir Mortimer B. Davis - Jewish General Hospital
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial helps cancer patients by collecting extra tumor samples left over from their regular diagnostic tests. Researchers use these samples to gain insights into cancer behavior. Participants also provide access to their medical records and agree to future contact for research projects. This trial suits adults with cancer who are willing to share their medical data and samples to support research. Known as the Personalize My Treatment (PMT) Registry, it aims to improve cancer treatment by understanding each person's unique cancer journey.

As an unphased trial, it offers patients the chance to contribute to groundbreaking research that could lead to more personalized cancer treatments.

What prior data suggests that the Personalize My Treatment (PMT) Registry is safe?

Research has shown that patient registries, such as the Personalize My Treatment (PMT) Registry, are generally safe. These registries collect real-world information about patient outcomes and safety without introducing new drugs or treatments, eliminating direct safety concerns from trying new medications. Instead, registries gather data from patients' existing medical records and samples. Well-designed registries offer a real-world view of medical practice and can uncover unique safety information. However, they do not involve the risks typically associated with new drug trials. Participants primarily share their data and samples, a process generally well-tolerated.12345

Why are researchers excited about this trial?

The Personalize My Treatment (PMT) Registry is exciting to researchers because it aims to tailor treatments specifically to individual patient needs, rather than using a one-size-fits-all approach. Unlike standard treatments that may not account for individual differences, this registry focuses on personalizing care, potentially leading to more effective and targeted outcomes. Researchers hope to learn which treatment strategies work best for specific patient profiles, ultimately enhancing the effectiveness and efficiency of healthcare by minimizing trial and error in treatment plans.

What evidence suggests that the Personalize My Treatment (PMT) Registry could be effective for cancer research?

Research has shown that patient registries, such as the Personalize My Treatment (PMT) Registry, provide a real-world perspective on treatment effectiveness. Well-designed registries enable doctors to observe patient responses and assess treatment efficacy over time. By collecting data from numerous patients, registries contribute to the development of improved and personalized treatment plans. Studies from cancer registries have demonstrated that their findings often align with those from controlled trials, indicating that registries can reliably reflect treatment outcomes outside strict clinical settings.12367

Who Is on the Research Team?

TR

Touhidur Rashid Opu, MD, MSc

Principal Investigator

Exactis Innovation

DB

David Bouffard, PhD

Principal Investigator

Exactis Innovation

Are You a Good Fit for This Trial?

Inclusion Criteria

Age of majority in the province of recruitment

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Biobanking

Participants provide residual clinical samples of their tumors for cancer research and consent to data collection from their medical records

Ongoing

Follow-up

Participants are monitored prospectively throughout the trajectory of their illness

Long-term

What Are the Treatments Tested in This Trial?

Interventions

  • Personalize My Treatment (PMT) Registry

Find a Clinic Near You

Who Is Running the Clinical Trial?

Sir Mortimer B. Davis - Jewish General Hospital

Lead Sponsor

Trials
61
Recruited
25,800+

Exactis Innovation

Lead Sponsor

Trials
9
Recruited
10,700+

Lady Davis Institute

Collaborator

Trials
50
Recruited
6,600+

McGill Centre for Translational Research in Cancer

Collaborator

Citations

Patient Registries - - NCBI - NIH

Properly designed and executed, patient registries can provide a real-world view of clinical practice, patient outcomes, safety, and comparative effectiveness.

Patient Registry Research for Health Outcomes

Custom Registry Design & Implementation - Build fit-for-purpose registries tailored to your therapeutic area, regulatory needs, and scientific objectives.

Patient Registry Strategies | Applied Clinical Trials Online

A registry should be seen as the primary vehicle for collecting long-term, observational data (usually from a large cohort of patients) to better understand the ...

Evaluation of the Use of Cancer Registry Data for ...

This comparative effectiveness study examines the concordance of data from an observational cancer registry with data from randomized ...

The Advantages of Healthcare Registries for Patients and ...

By analyzing data from large patient populations, registries help doctors develop more effective and personalized treatment plans.

Patient Registries in Clinical Research: Design, Benefits ...

In this blog, we will explore how patient registries are designed, the value they bring to clinical research, and some compelling use cases ...

A Practical Guide for Setting Up Patient Registries ...

Patient registries can reveal unique safety information, but it can be challenging to comply with pharmacovigilance guidelines (“the How”).