Macitentan for the Treatment of Digital Ulcers in Systemic Sclerosis Patients

• Status: Completed
• Trial end date: 2013-11-01
• Target enrollment: 0
• Participant gender: All

Summary

The DUAL-1 study is designed as a multicenter, double-blind two-period study with an initial fixed 16-week Period 1, followed by a Period 2 of variable duration. All patients completing Period 1 will continue on their original randomized treatment into Period 2, until the last randomized patient has completed Period 1.

Patients will be randomized in a 1:1:1 ratio (macitentan 3mg: macitentan 10mg: placebo).

The primary objective is to demonstrate the effect of macitentan on the reduction of the number of new digital ulcers in patients with systemic sclerosis and ongoing digital ulcers.

Other objectives include:

• the evaluation of the efficacy of macitentan on hand functionality and DU burden at Week 16 in SSc patients with ongoing DU disease.

• the evaluation of the safety and tolerability of macitentan in these patients.

• the evaluation of the efficacy of macitentan on time to first DU complication during the entire treatment period.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Actelion
• Treatments: Macitentan

Criteria

Inclusion Criteria :

• Patients ≥ 18 years of age

• Women of childbearing potential must use two reliable methods of contraception

• Diagnosis of SSc according to the classification criteria of the American College of Rheumatology (ACR)

• At least one visible, active ischemic digital ulcers (DU) at baseline

• History of at least one additional recent active ischemic DU

Exclusion Criteria :

• DUs due to condition other than SSc

• Symptomatic Pulmonary arterial hypertension (PAH)

• Body mass index (BMI) < 18 kg/m^2

• Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) > 1.5 x upper limit of the normal range (ULN)

• Hemoglobin < 75% of the lower limit of the normal range

• Systolic blood pressure < 95 mmHg or diastolic blood pressure < 50 mmHg

• Severe malabsorption; any severe organ failure (e.g., lung, kidney), or any life-threatening condition.

• Females who are pregnant or breastfeeding or plan to do so during the course of this study.

• Substance or alcohol abuse or dependence, or tobacco use at any level.

• Treatment with phosphodiesterase type-5 (PDE5) inhibitors.

• Patients on statins, who have received treatment for less than 3 months prior to Screening or whose treatment has not been stable during this period.

• Patients on vasodilators, who have received treatment for less than 2 weeks prior to Screening or whose treatment has not been stable during this period.

• Treatment with prostanoids within 3 months.

• Treatment with disease modifying agents if present for less than 3 months prior to Screening or whose treatment has not been stable for at least 1 month prior to Screening.

• Treatment with oral corticosteroids (> 10 mg/day of prednisone or equivalent).

• Treatment with ERAs within 3 months.

• Systemic antibiotics to treat infected DU(s) within 4 weeks.