Safety and Efficacy of SGN-LIV1A Plus Pembrolizumab for Patients With Locally-Advanced or Metastatic Triple-Negative Breast Cancer
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Seagen Inc.
- Study ID
- NCT03310957
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
- Triple Negative Breast Neoplasms
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- ladiratuzumab vedotin — DRUGGiven into the vein (IV; intravenously)
- Pembrolizumab — DRUGIV infusion every 3 weeks
Study Details
This trial studies ladiratuzumab vedotin (LV) with pembrolizumab in patients with triple-negative breast cancer. It will find out what side effects happen when participants get these two drugs. A side effect is anything the drugs do besides treating cancer. Pembrolizumab is a drug that can be used to treat triple-negative breast cancer. The trial will also find out if these drugs work to treat this type of cancer. Participants in this study have metastatic breast cancer. This means the cancer has spread to other parts of the body.
Key Dates
- Start date
- Feb 27, 2018
- Status verified
- Dec 2025
- Primary completion
- Sep 30, 2024
- Completion
- Sep 30, 2024
Study Design
- Enrollment
- 185 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: LV + pembrolizumabLV + pembrolizumab
Primary Outcome Measure
Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) [ Time Frame: From start of study treatment up to 30 days and up to 90 days post last dose for AEs and SAEs respectively (maximum exposure to any study treatment = 27 months; follow-up: AEs = maximum up to 28 months; SAEs = maximum up to 30 months) ]
Locations (26)
Related coverage on Hipa.ai
- Pembrolizumab + Ladiratuzumab Vedotin: TNBC Safety Data PostedPembrolizumab · Dec 12, 2025 · ClinicalTrials.gov
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