CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 396 enrolled
Drug / intervention
MSTT1041A +3 moredrug
Likely dose
MSTT1041A 700 milligramsfrom 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/NCT04386616
NCT04386616Phase 2Completed

A Phase II, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Safety and Efficacy of MSTT1041A or UTTR1147A in Patients With Severe COVID-19 Pneumonia

Genentech, Inc.·interventional·Posted May 13, 2020·Updated Jan 10, 2022

In Brief

A Phase 2 clinical trial evaluating MSTT1041A, MSTT1041A-matched Placebo, and 2 other interventions for COVID-19 Pneumonia. Completed, enrolled 396 participants across 41 sites in 4 countries.

Detailed Summary

This is a Phase II, randomized, double-blind, placebo-controlled, multicenter study to assess the efficacy and safety of MSTT1041A (astegolimab) compared with placebo and of UTTR1147A compared with placebo, in combination with standard of care (SOC), in patients hospitalized with severe coronavirus disease 2019 (COVID-19) pneumonia.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBrazil, Mexico, Spain, United States

Timeline

Phase 2CompletedFinished
202120222023202420252026
First PostedMay 13, 2020
Enrollment StartJun 2, 2020
Primary CompletionJan 8, 2021
Study CompletionFeb 12, 2021
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 6.1 years ago

Interventions

MSTT1041Adrug

Participants received one intravenous (IV) infusion of MSTT1041A 700 milligrams (mg) on Day 1. A second IV dose of MSTT1041A 350 mg was given on Day 15 if the participant remained hospitalized with a requirement for supplemental oxygen.

MSTT1041A-matched Placebodrug

Participants received up to 2 intravenous infusions of MSTT1041A-matched placebo.

UTTR1147Adrug

Participants received one intravenous (IV) infusion of UTTR1147A 90 micrograms/kilogram body weight (μg/kg) on Day 1. A second IV dose of UTTR1147A 90 μg/kg was given on Day 15 if the participant remained hospitalized with a requirement for supplemental oxygen.

UTTR1147A-matched Placebodrug

Participants received up to 2 intravenous infusions of UTTR1147A-matched placebo.