Clinical Trial

CAN1012 in Pre-Malignant DCIS and LCIS

Not Yet Recruiting Phase 1
View on ClinicalTrials.gov →
Summary
This is a Phase I/Ib study evaluating CAN1012 in patients with ductal carcinoma in situ and lobular carcinoma in situ.
Protocol Amendment History 2 changes
notable Enrollment reduced: 60 -> 24 participants 2026-04-09
minor Trial arms changed: 3 -> 4 2026-04-09
Trial Details
NCT Number NCT07408856
Lead Sponsor Providence Health & Services
Collaborators: CanWell Pharma Inc.
Conditions Ductal Carcinoma in Situ, Lobular Carcinoma in Situ
Enrollment 24 participants
Start Date 2026-08
Primary Completion 2030-05 (estimated)
Study Completion 2035-05 (estimated)
Updated on ClinicalTrials.gov 2026-07-23