A Double-Blinded Study to Evaluate the Safety, Tolerability, and Efficacy of BMS-986020 Versus Placebo in Diffuse Cutaneous Systemic Sclerosis (dcSSc)
Status: | Withdrawn |
---|---|
Conditions: | Skin and Soft Tissue Infections, Dermatology, Dermatology |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | February 2016 |
End Date: | October 2019 |
This is a two part study.
The purpose of Part A is to determine if BMS-986020 is effective in treatment of diffuse
cutaneous systemic sclerosis using one dose of BMS-986020.
The purpose of Part B is to determine if BMS-986020 is effective in treatment of diffuse
cutaneous systemic sclerosis using two different doses of BMS-986020.
The purpose of Part A is to determine if BMS-986020 is effective in treatment of diffuse
cutaneous systemic sclerosis using one dose of BMS-986020.
The purpose of Part B is to determine if BMS-986020 is effective in treatment of diffuse
cutaneous systemic sclerosis using two different doses of BMS-986020.
For more information regarding BMS clinical trial participation, please visit
www.BMSStudyConnect.com
Inclusion Criteria:
- Diagnosis of diffuse cutaneous systemic sclerosis for 60 months or less
- Men and women ≥ 18 years of age
- Ability to comply with birth control requirements
- Certain immunosuppressive agents are permitted
Exclusion Criteria:
- Limited cutaneous systemic sclerosis or sine scleroderma
- Active ulcers on fingers
- Pulmonary arterial hypertension
- Any gastrointestinal surgery that may impact absorption of study drug
We found this trial at
20
sites
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