Safety and PK Study of CC-90001 in Subjects With Pulmonary Fibrosis
NCT02510937 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 16
Last updated 2017-04-04
Summary
Participation in the study will last for 3months, with a 1 month screening phase.
Conditions
Interventions
- DRUG
-
CC-90001
Sponsors & Collaborators
-
Celgene
lead INDUSTRY
Principal Investigators
-
Ed O'Mara, MD · Celgene Corporation
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-08-05
- Primary Completion
- 2017-02-06
- Completion
- 2017-02-06
Countries
- United States
- Australia
Study Locations
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