Phase 2a Study to Evaluate the Efficacy and Safety of MEDI9929 in Adults With Atopic Dermatitis

PHASE2CompletedINTERVENTIONAL
Enrollment

113

Participants

Timeline

Start Date

August 15, 2015

Primary Completion Date

May 9, 2016

Study Completion Date

July 15, 2016

Conditions
Atopic Dermatitis
Interventions
BIOLOGICAL

MEDI9929

Participants will receive 6 subcutaneous doses of MEDI9929 280 mg every 2 weeks for 12 weeks, with the last dose at Week 10.

BIOLOGICAL

Placebo

Participants will receive 6 subcutaneous doses of placebo every 2 weeks for 12 weeks, with the last dose at Week 10.

Trial Locations (29)

2170

Research Site, Liverpool

3143

Research Site, Tauranga

3529

Research Site, Miskolc

4032

Research Site, Debrecen

6021

Research Site, Wellington

6720

Research Site, Szeged

7400

Research Site, Kaposvár

7632

Research Site, Pécs

9700

Research Site, Szombathely

10117

Research Site, Berlin

28277

Research Site, Charlotte

30625

Research Site, Hanover

33162

Research Site, North Miami Beach

33624

Research Site, Tampa

46032

Research Site, Carmel

46256

Research Site, Indianapolis

48149

Research Site, Münster

60005

Research Site, Arlington Hts

60590

Research Site, Frankfurt am Main

80337

Research Site, München

97239

Research Site, Portland

08009

Research Site, Berlin

02606

Research Site, ACT

04102

Research Site, Woolloongabba

V3R 6A7

Research Site, Surrey

L4M 6L2

Research Site, Barrie

G1V 4X7

Research Site, Québec

07548

Research Site, Gera

04103

Research Site, Leipzig

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Amgen

INDUSTRY

lead

MedImmune LLC

INDUSTRY

NCT02525094 - Phase 2a Study to Evaluate the Efficacy and Safety of MEDI9929 in Adults With Atopic Dermatitis | Biotech Hunter | Biotech Hunter