Purpose of this Study
We are doing this study to find out if an experimental drug called ADI-PEG 20 (the study drug) combined with two types of FDA-approved chemotherapies (gemcitabine and docetaxel) is a safe and effective option for people who have leiomyosarcoma.
Who Can Participate?
Eligibility
Adults ages 18+ who are diagnosed with leiomyosarcoma.
For more information about who can participate in this study, please contact the study team at alicia.wilkerson@duke.edu.
What is Involved?
Description
If you choose to join this study, during the screening period you will:
- Have a physical exam
- Have blood draws
- Have imaging scans (CT or MRI)
- Have an electrocardiogram (ECG) to check your heart function
- Visit the clinic for various tests to see if you are eligible to proceed to the study drug period
- Group 1 will receive the study drug in combination with gemcitabine and docetaxel
- Group 2 will receive a placebo (inactive substance with no drug in it) in combination with gemcitabine and docetaxel
- You will get your first dose of the study drug or placebo a week before your first cycle begins
- You will get a shot of the study drug/placebo on the 1st, 8th, and 15th day of each cycle
- You will get gemcitabine on the 1st and 8th days of each cycle
- You will get docetaxel on the 8th day of each cycle
Study Details
Full Title
ADI-PEG 20 (Pegargiminase) or Placebo (PBO) plus Gemcitabine and Docetaxel in Previously Treated Subjects with Leiomyosarcoma (ARGSARC): A Randomized, Double-Blind, Multi-Center Phase 3 Trial
Principal Investigator
Juneko
Grilley Olson
Protocol Number
PRO00113455
NCT ID
NCT05712694
Phase
III
Enrollment Status
Open to Enrollment