Repare RP-3500-01 (Advanced Solid Tumors) - Clinical Trial
What is the Purpose of this Study?
We are doing this study to find out the safest and most effective dose of the study drug (RP-3500) when it is given alone or in combination with talazoparib.
What is the Condition Being Studied?
Advanced Solid Tumors
Who Can Participate in the Study?
Adults with advanced cancer resistant to standard treatment with documented changes in certain genes.
For more information, contact the study team at 919-684-6342.
Age Group
Adults
What is Involved?
If you choose to join this study you will:
- Go through a screening period to see if you qualify for the study
- Take the study drug (RP-3500) by mouth 1 or 2 times a day according to the assigned schedule
- Provide old tumor tissue
- Have physical exams, blood and urine tests
- Have imaging scans (CT and/or MRI)
Some people will also:
- Take talazoparib by mouth once daily
- Have tumor samples taken
Study Details
Full Title
Phase 1/2a Study of the Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Clinical Activity of RP-3500 Alone or in Combination with Talazoparib or Gemcitabine in Advanced Solid Tumors with ATR inhibitor Sensitizing Mutations (TRESR Study)
Principal Investigator
Medical Oncologist
Protocol Number
IRB:
PRO00106181
NCT:
NCT04497116
Phase
Phase
I/II
ClinicalTrials.gov
View on ClinicalTrials.gov
Enrollment Status
Open for Enrollment
Participate
Call 919-684-6342