Safety and Immunogenicity of MSB11455 in Healthy Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

336

Participants

Timeline

Start Date

August 21, 2017

Primary Completion Date

February 5, 2018

Study Completion Date

September 22, 2018

Conditions
Healthy
Interventions
DRUG

MSB11455

Participants received a single subcutaneous injection of MSB11455 6 milligram (mg) per (/) 0.6 milliliter (mL) on Day 1 in morning of treatment period 1 (28 Days) and 2 (28 Days). Period 1 and Period 2 are separated by a washout period of 35 Days.

DRUG

US-Neulasta

Participants received a single subcutaneous injection of US-Neulasta 6 mg/0.6 mL on Day 1 in morning of treatment period 1 and 2. Period 1 and Period 2 are separated by a washout period of 35 Days.

Trial Locations (2)

1150

Auckland Clinical Studies Ltd, Auckland

8001

Christchurch Clinical Studies Trust, Christchurch

All Listed Sponsors
lead

Fresenius Kabi SwissBioSim GmbH

INDUSTRY

NCT03251339 - Safety and Immunogenicity of MSB11455 in Healthy Participants | Biotech Hunter | Biotech Hunter