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

No results posted yet for this study

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02510937 on ClinicalTrials.gov