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Anti-metabolites
Paclitaxel + Folic Acid + Lometrexol for Cancer
Phase 1
Waitlist Available
Research Sponsored by Jonsson Comprehensive Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
No inflammatory bowel disease, No radiation enteritis, No malabsorption syndrome
Histologically or cytologically proven locally advanced or metastatic solid tumor that is refractory to standard therapies or for which there are no therapies of potential major benefit
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial is studying how well giving paclitaxel, folic acid, and lometrexol together works in treating patients with solid tumors.
Who is the study for?
This trial is for adults with advanced or metastatic solid tumors that haven't responded to standard treatments. Participants must have a life expectancy of at least 12 weeks, measurable disease, and no severe illnesses that could interfere with the study. They should not be pregnant or nursing and must use contraception if fertile.Check my eligibility
What is being tested?
The trial tests a combination of paclitaxel (a chemotherapy drug), folic acid (which may protect normal cells and make tumor cells more sensitive to treatment), and lometrexol (an enzyme blocker) in patients with advanced solid tumors to see if this mix can better kill cancer cells.See study design
What are the potential side effects?
Potential side effects include those typical of chemotherapy such as nausea, fatigue, hair loss, increased risk of infection due to low blood cell counts, nerve damage leading to numbness or tingling sensations, and allergic reactions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I do not have inflammatory bowel disease, radiation enteritis, or malabsorption syndrome.
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My advanced cancer does not respond to standard treatments.
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I am fully active or able to carry out light work.
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I am 18 years old or older.
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My cancer can be measured by tests.
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My liver function tests are within the required range.
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My kidneys filter blood at a rate of at least 65 mL/min.
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
Find a Location
Who is running the clinical trial?
National Cancer Institute (NCI)NIH
13,687 Previous Clinical Trials
40,930,371 Total Patients Enrolled
Jonsson Comprehensive Cancer CenterLead Sponsor
361 Previous Clinical Trials
27,782 Total Patients Enrolled
Lee S. Rosen, MDStudy ChairJonsson Comprehensive Cancer Center
5 Previous Clinical Trials
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not have fluid buildup causing symptoms unless it was drained.It's been over 4 weeks since my last chemotherapy, and I'm not on other cancer-killing drugs.I do not have inflammatory bowel disease, radiation enteritis, or malabsorption syndrome.I have recovered from my last radiotherapy and haven't had it on more than 25% of my bone marrow. I'm not currently receiving any radiotherapy.I haven't taken experimental drugs or certain antibiotics recently and had no more than 2 treatments for advanced cancer.I am not on any hormonal therapy.It's been over 4 weeks since my last major surgery and I've recovered.My advanced cancer does not respond to standard treatments.I am fully active or able to carry out light work.My cancer has not spread to my brain or spinal cord.I am not currently taking any medication to boost my white blood cells or red blood cells.I am 18 years old or older.My cancer can be measured by tests.My liver function tests are within the required range.I do not have blood cancer such as leukemia, lymphoma, or multiple myeloma.My kidneys filter blood at a rate of at least 65 mL/min.
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.
Is enrollment still available for this research trial?
"The clinicaltrials.gov page for this research indicates that the study is not currently looking to add any more patients, having been initially posted in September of 2001 with an update made on September 16th 2013. However, there are still 83 other trials actively recruiting participants at present."
Answered by AI
What potential perils exist for individuals undergoing this procedure?
"As this is a Phase 1 trial, our team at Power has rated its safety as a 1 due to the reduced amount of evidence supporting both effectiveness and security."
Answered by AI
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