A Study in Adult Subjects With Select Advanced Solid Tumors

NCT02583165 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2019-01-08

No results posted yet for this study

Summary

To evaluate the safety and tolerability of MEDI1873 in adult subjects with selected advanced solid tumors.

Conditions

Interventions

BIOLOGICAL

MEDI1873

Subjects will receive MEDI1873 by intravenous administration

Sponsors & Collaborators

  • MedImmune LLC

    lead INDUSTRY

Principal Investigators

  • Medimmune LLC · MedImmune LLC

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-09
Primary Completion
2018-12-19
Completion
2018-12-19

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02583165 on ClinicalTrials.gov