A Study of CNTO 3157 in Healthy Normal and Asthmatic Participants Inoculated With Human Rhinovirus Type 16

PHASE1CompletedINTERVENTIONAL
Enrollment

76

Participants

Timeline

Start Date

October 31, 2012

Primary Completion Date

November 30, 2014

Study Completion Date

November 30, 2014

Conditions
Healthy Volunteers and Asthma
Interventions
DRUG

CNTO 3157 (healthy participants)

CNTO 3157 10 mg/kg, as a single intravenous infusion, on Day 1, 24 to 72 hours prior to inoculation with human rhinovirus type 16 (HRV-16).

DRUG

Placebo (healthy participants)

Placebo, as a single intravenous infusion, on Day 1, 24 to 72 hours prior to inoculation with HRV-16.

DRUG

CNTO 3157 (asthmatic patients)

CNTO 3157 10 mg/kg, as a single intravenous infusion, at Week 1 (Day 1), followed by 3 infusions of 3 mg/kg of CNTO 3157 at Week 2 (Day 8), Week 3 (Day 15), and Week 4 (Day 22). The final infusion (Week 4) will occur 24 to 72 hours prior to inoculation with HRV-16.

DRUG

Placebo (asthmatic patients)

Placebo, as 4 intravenous infusions, at Week 1 (Day 1), Week 2 (Day 8), Week 3 (Day 15), and Week 4 (Day 22). The final infusion (Week 4) will occur 24 to 72 hours prior to inoculation with HRV-16.

OTHER

HRV-16

Single inoculation of HRV-16 in a total volume of approximately 1.0 mL, administered as 2 instillations per naris.

Trial Locations (13)

Unknown

Antwerp

Calgary

Halifax

Hellerup

København NV

Borstel

Frankfurt

Amsterdam-Zuidoost

Groningen

Belfast

Dundee

London

Manchester

All Listed Sponsors
lead

Janssen Research & Development, LLC

INDUSTRY

NCT01704040 - A Study of CNTO 3157 in Healthy Normal and Asthmatic Participants Inoculated With Human Rhinovirus Type 16 | Biotech Hunter | Biotech Hunter