Condition: Endometrial Cancer · Ovarian Cancer · Cervical Cancer · Sponsor: Advenchen Laboratories, LLC
The purpose of Part 1 (Phase 1b) is to evaluate the general safety and tolerability of repeated 21-day cycles of AL3818 therapy, and to reevaluate the maximum tolerated dose (MTD). The purpose of Part 2 (Phase 2a) is to evaluate the efficacy of repeated 21-day cycles of AL3818 therapy preliminary efficacy of AL3818 in subjects with recurrent or metastatic endometrial, ovarian or cervical cancer.
This description comes directly from the study's public registry record.
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| University of Chicago Medical Center | Chicago, Illinois, United States | — |
| Huntsman Cancer Institute, University of Utah | Salt Lake City, Utah, United States | — |
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Source record: clinicaltrials.gov/study/NCT02558348