CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 86 enrolled
Drug / intervention
Trastuzumab deruxtecan +1 moredrug
Likely dose
Nivolumab 10 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03523572
NCT03523572Phase 1Completed

A Phase 1b, Multicenter, Two-Part, Open-Label Study of Trastuzumab Deruxtecan, an Anti-Human Epidermal Growth Factor Receptor-2 (HER2)-Antibody Drug Conjugate (ADC), in Combination With Nivolumab, an Anti-PD-1 Antibody, for Subjects With HER2-expressing Advanced Breast and Urothelial Cancer

Daiichi Sankyo·interventional·Posted May 14, 2018·Updated Jan 27, 2025

In Brief

A Phase 1 clinical trial evaluating Trastuzumab deruxtecan and Nivolumab for Breast Cancer and Urothelial Carcinoma. Completed, enrolled 86 participants across 29 sites in 7 countries.

Detailed Summary

This is a study of trastuzumab deruxtecan for the treatment of HER2-positive unresectable or metastatic breast cancer following two or more prior anti-HER2 based regimens. Participants will receive this study drug along with a cancer drug, an immune checkpoint inhibitor, anti-PD1, called nivolumab. The study will be done in two parts: * Part 1 is to identify the recommended dose to use for treatment. * Part 2 is to find out how well the combination works, and how safe and tolerable it is.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelgium, France, Germany, Italy, Spain, United Kingdom, United States

Timeline

Phase 1CompletedFinished
20192020202120222023202420252026
First PostedMay 14, 2018
Enrollment StartAug 2, 2018
Primary CompletionJul 22, 2021
Study CompletionSep 12, 2023
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 8.1 years ago

Interventions

Trastuzumab deruxtecandrug

The investigational product is a sterile lyophilized powder, which is made into solution for intravenous administration.

Nivolumabdrug

Nivolumab is an aqueous solution formulated at 10 mg/mL to be administered at a flat dose of 360 mg IV over 30 minutes. Protocol-defined thyroid testing is required while taking nivolumab.