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ARC101 in Advanced Solid Tumors
RecruitingPhase 1
A Phase 1 Study of ARC101 in Advanced Solid Tumors
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
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 * Active autoimmune disease within 12 months prior to first dose of study drug. * Female participant who is pregnant, breastfeeding, or plans to become pregnant or male participant who plans to father a child either while enrolled or within 90 days after the final administration of study drug.
About the study
This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of ARC101 in patients with advanced cancer.
What is being tested
- ARC101 (drug)
Sponsor: Third Arc Bio · Participants: 70 · Started: Feb 5, 2025
Contact the study team
- VP Clinical Operations · Phone: 267-589-9444
Official record on ClinicalTrials.gov — NCT06672185
Locations in the U.S.
| Michigan | START Midwest, Grand Rapids |
| Texas | START San Antonio, LLC., San Antonio |
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.