UT-15C SR in the Treatment of Critical Limb Ischemia

NCT ID: NCT00445159

Last Updated: 2007-03-08

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-11-30

Brief Summary

This study will evaluate UT-15C sustained release tablets in subjects experiencing ischemic lower limb rest pain related to advanced peripheral arterial disease. Rest pain is one of the primary management issues of severe arterial occlusive disease and may lead to amputation when the pain becomes intolerable and unresponsive to narcotic analgesia. Rest pain also impacts the quality of sleep and mobility with frequent interruptions in sleep and decreased mobility. Treprostinil sodium (Remodulin®) has been studies in several small open-label studies and has been shown to be safe as well as an effective agent for ischemic rest pain when given by subcutaneous or intravenous delivery. However, these forms of administration have patient convenience limitations, including the need for an infusion device and associated pain at the site of infusion with subcutaneous delivery. UT-15C may allow patients suffering from CLI to benefit from the simplicity of an oral dosage form

Detailed Description

This study is an eight week, two center, open-label study assessing the tolerability, safety, and efficacy of oral UT-15C sustained release tablets in subjects with CLI and ischemic lower limb rest pain, with or without an ischemic wound present. Conventional therapy should be continued without changes over the course of the study for all subjects.

Group 1: The first ten subjects to enroll in the study will be assigned to receive an initial dose of 1mg. The dose will be titrated upward every seven days, depending on tolerability, to a maximum dose of 4mg/day .

Group 2: The last ten subjects to enroll in the study will be assigned to receive an initial dose of 1mg. The dose will be titrated upward every seven days, depending on tolerability to a maximum dose of 8 mg/day .

Conditions

Critical Limb Ischemia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Interventions

UT-15C SR (treprostinil diethanolamine) 1mg oral tablets

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Have an ankle systolic pressure ≤ 60 mm/Hg OR ABI ≤ 0.60 OR toe systolic pressure ≤ 60 mm/Hg OR an arteriogram showing at least one level of occlusion of lower extremity arteries.

2. Have been taking analgesics to control ischemic rest pain for at least two weeks at Baseline.

3. Have signed an appropriate consent for participation in this study.

4. If female, be physiologically incapable of childbearing or practicing acceptable methods of birth c

Exclusion Criteria

1. Have had a vascular surgery or other vascular procedure to treat their CLI within 30 days prior to study entry.

2. Have a planned or scheduled vascular surgery or endovascular procedure.

3. Be currently taking any investigational drugs for CLI.

4. Have received prostaglandins such as PGE1, epoprostenol (Flolan®), or any other prostacyclin (PGI2) or prostacyclin analog in the past 30 days.

5. Be hemodynamically unstable or have acute renal failure, cardiac failure or pulmonary failure.

6. Have a diagnosis of Stage IVb (Fontaine) or Stage 6 (Rutherford scale) Critical Limb Ischemia due to documented peripheral arterial disease

7. Have an unhealed incision(s) from a toe or transmetatarsal amputation at Baseline.

8. Have any wound with significant gangrene or exposed tendons.

• Minimum Eligible Age: 45 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Southern Illinois University

OTHER

Sponsor Role: collaborator

Southern Arizona Vascular Institute

OTHER

Sponsor Role: lead

Principal Investigators

Colleen Johnson, MD

Role: PRINCIPAL_INVESTIGATOR

Southern Illinois University

Scott S Berman, MD

Role: PRINCIPAL_INVESTIGATOR

Southern Arizona Vascular Institute

Locations

Southern Arizona Vascular Institute

Tucson, Arizona, United States

Site Status: RECRUITING

Southern Illinois University School of Medicine

Springfield, Illinois, United States

Site Status: RECRUITING

Countries

United States

Facility Contacts

Sonia Voigt, RN

Role: primary

svoigt@azvasc.com

520-297-5846

Carol Buettner

Role: primary

cbuettner@siumed.edu

217-545-2320

Other Identifiers

UT-15C

Identifier Type: -

Identifier Source: org_study_id