No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
100 (estimated)
Sponsor
British Columbia Cancer Agency · Other
Who this trial is looking for
This trial is looking for people with cancer who want to share their experience with a treatment that is being studied for its effectiveness. Participants will be asked to provide information about their quality of life and survival after starting the treatment.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with cancer.
I can expect to live at least 12 more weeks.
I have good blood and organ function as assessed by my doctor.
I am not currently pregnant or breastfeeding.
I can provide informed consent for the study.
You may not be able to join if
I have taken any treatment for my cancer in the last 14 days.
I cannot complete quality of life questionnaires.
I have major heart issues or serious infections that could make the treatment unsafe.
My doctor thinks I am unfit for this study.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria:
* 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 …
Inclusion Criteria:
* 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 (refrain from heterosexual intercourse) or use contraceptive methods that result in a failure rate of less than 1% per year during the treatment period and for at least 5 months after the last dose.
* For men: agreement to remain abstinent (refrain from heterosexual intercourse with a female partner of childbearing potential or who is pregnant) or use contraceptive measures, and agreement to refrain from donating sperm, during the treatment period and for at least 5 months after the last dose.
* Ability to give informed consent for the study procedures defined in this protocol.
Exclusion Criteria:
* 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.
* Any significant cardiovascular disease, comorbidity (i.e. recent major infection, HIV, tuberculosis) or major surgical procedure within 21 days that in the opinion of the investigator renders the proposed treatment unsafe.
* Subjects who are otherwise felt by the treating clinician to be unfit to proceed with this protocol.
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