Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06242912

Evidence Development in Cancer Treatment - Real World: PREDiCTrw

Led by British Columbia Cancer Agency · Updated on 2025-09-25

100

Participants Needed

1

Research Sites

258 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This pilot clinical trial aims to assess the real world quality of life and survival of patients treated with therapy that has preliminary evidence of efficacy but uncertainty of the magnitude of clinical benefit or cost effectiveness in subjects with cancer. The goal of this study is to collect real world evidence with respect to quality of life and outcomes to support decision making.

CONDITIONS

Official Title

Evidence Development in Cancer Treatment - Real World: PREDiCTrw

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects with cancer for which there remains ongoing questions regarding clinical effectiveness and/or cost effectiveness regarding a therapeutic agent
  • Eastern Co-operative Group (ECOG) 0-2
  • Life expectancy of at least 12 weeks
  • Adequate hematologic and end organ function for drug treatment per the clinician's assessment
  • Asymptomatic or treated brain metastases permitted
  • For women of childbearing potential: agreement to remain abstinent or use contraceptive methods with failure rate less than 1% per year during treatment and for 5 months after last dose
  • For men: agreement to remain abstinent or use contraceptive measures and refrain from donating sperm during treatment and for 5 months after last dose
  • Ability to give informed consent for the study procedures
Not Eligible

You will not qualify if you...

  • Treatment with any approved or investigational agent or participation in another clinical trial with therapeutic intent within 14 days prior to enrollment
  • Inability to complete quality of life questionnaires
  • Pregnancy or breastfeeding
  • Significant cardiovascular disease, comorbidity, or major surgery within 21 days considered unsafe by investigator
  • Subjects considered unfit by treating clinician to proceed with this protocol

AI-Screening

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Trial Site Locations

Total: 1 location

1

BC Cancer

Vancouver, British Columbia, Canada, V5Z4E6

Actively Recruiting

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Research Team

C

Cheryl Ho, MD

CONTACT

H

Howard Lim, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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Evidence Development in Cancer Treatment - Real World: PREDiCTrw | DecenTrialz