CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 57 enrolled
Drug / intervention
RC48-ADCdrug
Likely dose
Not stated in 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/NCT02881190
NCT02881190Phase 1Completed

A Tolerance, Safety and Pharmacokinetic Ascending Dose Phase I Study of RC48-ADC Administered Intravenously to Subjects With HER2-Positive Malignant in Advanced Malignant Solid Tumors

RemeGen Co., Ltd.·interventional·Posted Aug 26, 2016·Updated Jun 4, 2020

In Brief

A Phase 1 clinical trial evaluating RC48-ADC for Solid Tumors. Completed, enrolled 57 participants across 1 site.

Detailed Summary

A tolerance, safety and pharmacokinetic ascending dose phase I Study of RC48-ADC administered intravenously to subjects with HER2-positive malignant in advanced malignant solid tumors.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSolid Tumors
CountriesChina
Collaborators--

Timeline

Phase 1CompletedFinished
20162017201820192020202120222023202420252026
First PostedAug 26, 2016
Enrollment StartDec 14, 2015
Primary CompletionJun 27, 2019
Study CompletionNov 8, 2019
TodayJul 1, 2026
Enrollment to primary: 3.5 yearsPosted 9.8 years ago

Interventions

RC48-ADCdrug