CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 3 enrolled
Drug / intervention
rovalpituzumab tesirine +1 moredrug
Likely dose
rovalpituzumab tesirine 0.3 mg/kgfrom 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/NCT03543358
NCT03543358Phase 2Completed

A Multicenter, Long-Term, Rollover Extension Study of Rovalpituzumab Tesirine

AbbVie·interventional·Posted Jun 1, 2018·Updated Jan 5, 2021

In Brief

A Phase 2 clinical trial evaluating rovalpituzumab tesirine for Cancer. Completed, enrolled 3 participants across 3 sites.

Detailed Summary

The purpose of this long-term, extension study is to provide ongoing safety and efficacy follow-up of subjects who participated in a rovalpituzumab tesirine study that has completed the primary analysis and that is closing.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCancer
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedJun 1, 2018
Enrollment StartSep 10, 2018
Primary CompletionNov 26, 2019
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 8.1 years ago

Interventions

rovalpituzumab tesirinedrug

Optional retreatment with rovalpituzumab tesirine (0.3 mg/kg or previously adjusted dose) administered intravenously once every 6 weeks beginning on Day 1 (day of dosing) for 2 dose cycles

rovalpituzumab tesirinedrug

Rovalpituzumab tesirine (0.3 mg/kg or previously adjusted dose) administered intravenously once every 6 weeks beginning on Day 1 (day of dosing). Subjects will receive rovalpituzumab tesirine on Day 1 of each 6-week cycle, omitting every third cycle until disease progression or study drug discontinuation.