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111In-DAC Imaging Agent for Lung and Brain Cancer
Phase 1
Waitlist Available
Research Sponsored by Copharos
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Have an ECOG performance status of Zero or One
Are being evaluated for known or suspected non-small-cell lung cancer (NSCLC), or known brain lesions consistent with metastatic lung cancer
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial is investigating the safety and efficacy of a new imaging agent for brain and lung cancer.
Who is the study for?
This trial is for adults over 18 with lung cancer or brain tumors linked to lung cancer, who haven't had treatment yet. They must be scheduled for a biopsy or have a recent diagnosis and agree to use birth control. People with severe allergies, unstable health conditions, kidney or liver issues, or those on certain medications can't join.Check my eligibility
What is being tested?
The study tests the safety and effectiveness of a new imaging agent called 111In-DAC in detecting lung and brain cancers using planar and SPECT imaging techniques. It aims to improve how we see these cancers inside the body.See study design
What are the potential side effects?
Potential side effects may include allergic reactions to components of the imaging agent. Since it's used for scanning purposes, other risks might be related to exposure to radiation during image capture.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am fully active or can carry out light work.
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I am being checked for lung cancer or brain lesions from lung cancer.
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I have brain symptoms from lung cancer and haven't had brain radiation.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
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Who is running the clinical trial?
CopharosLead Sponsor
1 Previous Clinical Trials
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have had cancer before, but it was not serious skin cancer or cervical cancer.I am an adult who is not pregnant or breastfeeding and will use birth control during and after the study.I am fully active or can carry out light work.I do not have any severe illnesses, infections, or major organ problems.I cannot stay still during scans.I have taken medication that could harm my kidneys in the last 2 weeks.I am being checked for lung cancer or brain lesions from lung cancer.I have brain symptoms from lung cancer and haven't had brain radiation.I had a biopsy within the last 4 days before starting the study drug.I am diagnosed with lung cancer and have not started treatment yet.I have not received an indium agent in the last 30 days.
Research Study Groups:
This trial has the following groups:Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Do seniors aged 75 or older qualify for this investigation?
"This clinical trial only permits individuals aged 18 to 65. There are 407 trials that admit minors, while 4577 studies accept seniors as participants."
Answered by AI
What potential risks should be considered when administering this treatment?
"Due to the limited data available on safety and efficacy, this treatment is assigned a score of 1 for its risk profile."
Answered by AI
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