Clinical Trials Directory

Trials / Completed

CompletedNCT02900157

Study to Evaluate the Safety and Pharmacokinetics of MEDI9090 in Subjects With Advanced Solid Tumors

A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of MEDI9090 in Subjects With Advanced Solid Tumors

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
42 (actual)
Sponsor
MedImmune LLC · Industry
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

This is an open-label, study of MEDI9090 to evaluate the safety, tolerability, PK, immunogenicity, and antitumor activity of MEDI9090 in adult subjects with advanced solid tumors.

Conditions

Interventions

TypeNameDescription
BIOLOGICALMEDI9090MEDI9090 will be administered by IV infusion
BIOLOGICALDurvalumabDurvalumab as a single agent will be administered by IV infusion after patients have completed the prescribed doses of Medi9090.

Timeline

Start date
2016-08-09
Primary completion
2020-01-23
Completion
2020-01-23
First posted
2016-09-14
Last updated
2021-01-14

Locations

8 sites across 2 countries: United States, Japan

Source: ClinicalTrials.gov record NCT02900157. Inclusion in this directory is not an endorsement.