A Phase 1 Study of ARC101 in Advanced Solid Tumors
Third Arc Bio
Summary
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of ARC101 in patients with advanced cancer.
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: * Locally advanced or metastatic solid tumor ovarian, testicular or other Claudin 6+ cancers * Measurable or evaluable disease, per RECIST v1.1 * Eastern Cooperative Oncology Group (ECOG) performance status 0-1 * Adequate organ function Exclusion Criteria: * Active CNS involvement * Malignancy diagnosis other than the disease under study within 2 years prior to the first dose of study drug. * Presence of uncontrolled ascites * Toxicity related to prior anticancer therapy that has not returned to Grade ≤1 or baseline levels * Clinically significant pulmonary compromise *…
Interventions
- DrugARC101
ARC101 will be administered according to an assigned dose schedule.
Locations (12)
- Massachusetts General HospitalBoston, Massachusetts
- START MidwestGrand Rapids, Michigan
- START San Antonio, LLC.San Antonio, Texas
- Sunshine Coast University Private HospitalBirtinya, Queensland
- Cancer Research SAAdelaide, South Australia
- Cabrini Health ResearchMalvern, Victoria