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Farnesyl Transferase Inhibitor
R115777 + Topotecan for Cancer
Phase 1
Waitlist Available
Research Sponsored by National Center for Research Resources (NCRR)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Radiotherapy to less than 25% of bone marrow volume (no pelvic radiation)
Recovery from the effects of prior chemotherapy and radiation therapy, with at least a 4 week interval. All prior toxicities should have resolved to baseline prior to entry into the study
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial is designed to find the maximum tolerated dose of the combination of R115777 and topotecan in patients with advanced solid tumors.
Who is the study for?
This trial is for adults with advanced solid tumors who've had less than four chemo treatments and no recent infections. They should be in good health otherwise, not pregnant or breastfeeding, willing to use birth control, and have a life expectancy of at least six months. They must also have recovered from any previous treatments.Check my eligibility
What is being tested?
The study tests combining R115777, which may block cancer growth by targeting the p21 ras gene, with topotecan that attacks cells ignoring normal growth controls. This mix could work better together and R115777 can be taken orally.See study design
What are the potential side effects?
Potential side effects include those common to chemotherapy such as nausea, fatigue, hair loss, blood cell count changes increasing infection risk; specific effects of R115777 are not detailed but may involve organ function issues.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have received radiation that did not cover more than 25% of my bone marrow and did not include my pelvis.
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I have recovered from my last cancer treatment and it's been at least 4 weeks.
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I do not have stomach or intestine problems affecting medication absorption.
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I have had 3 or fewer chemotherapy treatments.
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I have not been on medication for an infection in the week before starting chemotherapy.
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?
National Center for Research Resources (NCRR)Lead Sponsor
537 Previous Clinical Trials
317,016 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have received radiation that did not cover more than 25% of my bone marrow and did not include my pelvis.I have recovered from my last cancer treatment and it's been at least 4 weeks.I do not have stomach or intestine problems affecting medication absorption.My organs are working well.I am using effective birth control methods.I have advanced cancer and standard treatments haven't worked well for me.I have had 3 or fewer chemotherapy treatments.I have not been on medication for an infection in the week before starting chemotherapy.
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.
How reliable is this therapy for providing a desirable outcome?
"Minimal clinical evidence exists to support the safety and efficacy of this treatment, which earns it a score of 1."
Answered by AI
Is this experiment accepting individuals who are 45 years of age or older?
"This trial's inclusion criteria stipulates that participants must be of adult age (18+ years old) and not exceed the maximum age threshold (65 years or younger)."
Answered by AI
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