CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 9 enrolled
Drug / intervention
MGC018drug
Likely dose
MGC018 2.7 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/NCT06227546
NCT06227546Phase 2Active

A Phase II Study of MGC018 in Patients With Relapsed or Refractory Extensive-Stage Small-Cell Lung Cancer (ES-SCLC)

Georgetown University·interventional·Posted Jan 29, 2024·Updated Jun 25, 2026

In Brief

A Phase 2 clinical trial evaluating MGC018 for Extensive-stage Small-cell Lung Cancer. Active but no longer recruiting, targeting 9 participants across 1 site.

Detailed Summary

The goal of this clinical trial is to test MGC018 in patients with relapsed or refractory Extensive-Stage Small-Cell Lung Cancer (ES-SCLC). The main question it aims to answer is: • Does the administration of MGC018 achieve a clinically meaningful response rate of 25% in patients with relapsed or refractory ES-SCLC? Participants enrolled in the trial will receive MGC018 through an intravenous (IV) infusion, every 28 days until disease progression or unacceptable toxicity. Tumor assessment will be done every 2 cycles (28 day cycles). Blood samples will be taken for biomarker analysis before treatment, on cycle 3 day 1, and at progression. A pretreatment biopsies will be done.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsMacroGenics

Timeline

Phase 2Active
2024202520262027
First PostedJan 29, 2024
Enrollment StartApr 15, 2024
Primary CompletionMar 28, 2025
Study CompletionApr 1, 2027
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 2.4 years ago

Interventions

MGC018drug

Intravenous (IV) Infusion, 2.7 mg/kg on Day 1 of each 28 day cycle