A Study to Evaluate the Safety of the Respiratory Syncytial Virus Vaccine MEDI7510 in Older Adults

PHASE1CompletedINTERVENTIONAL
Enrollment

246

Participants

Timeline

Start Date

April 30, 2014

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2015

Conditions
Respiratory Syncytial Virus (RSV)
Interventions
BIOLOGICAL

Placebo

Participants will receive placebo (sterile saline for human use from commercial source liquid) on Day 1.

BIOLOGICAL

RSV sF 20 mcg

Participants will receive single dose of 20 mcg RSV sF by intramuscular injection on Day 1.

BIOLOGICAL

MEDI7510 (20 mcg RSV sF)

Participants will receive single dose of MEDI7510 containing 20 mcg RSV sF by intramuscular injection on Day 1.

BIOLOGICAL

RSV sF 50 mcg

Participants will receive single dose of 50 mcg RSV sF by intramuscular injection on Day 1.

BIOLOGICAL

MEDI7510 (50 mcg RSV sF)

Participants will receive single dose of MEDI7510 containing 50 mcg RSV sF by intramuscular injection on Day 1.

BIOLOGICAL

RSV sF 80 mcg

Participants will receive single dose of 80 mcg RSV sF by intramuscular injection on Day 1.

BIOLOGICAL

MEDI7510 (80 mcg RSV sF)

Participants will receive single dose of MEDI7510 containing 80 mcg RSV sF by intramuscular injection on Day 1.

Trial Locations (3)

20850

Accelovance, Inc, Rockville

32806

Compass Research, Orlando

33143

Miami Research Associates, Miami

Sponsors

Lead Sponsor

All Listed Sponsors
lead

MedImmune LLC

INDUSTRY

NCT02115815 - A Study to Evaluate the Safety of the Respiratory Syncytial Virus Vaccine MEDI7510 in Older Adults | Biotech Hunter | Biotech Hunter