SANGUINATE™ in Sickle Cell Disease Associated Leg Ulcer (LU)

An Open-label, Repeated-dose, Dose Escalation Study of the Safety and Effectiveness of SANGUINATE™ for the Treatment of Leg Ulcers in Adult Patients With Sickle Cell Disease

SANGUINATE™ Sickle Cell Disease associated Leg Ulcers.

Study Overview

• Status: Completed
• Conditions: Leg Ulcer
• Intervention / Treatment: Biological: SANGUINATE

Detailed Description

This is an escalating, repeated-dose, open-label Phase 2 study to test SANGUINATE (pegylated carboxyhemoglobin bovine) in patients suffering from leg ulceration associated with Sickle Cell Disease (SCD leg ulcer).

Patients will undergo consent and screening procedures at the time of presentation for leg ulcer treatment. Eligible patients will begin a 3-week Run-In Period. A total of approximately fifteen (15) patients are expected to be screened in order to achieve an enrollment target of ten (10) evaluable patients for participation in the study. Evaluable is defined as a patient receiving a minimum of three doses of investigational product. Five (5) patients (Cohort 1) will receive four (4) once-weekly 2-hour IV infusions of SANGUINATE at a dose of 320 mg/kg (8 mL). An additional five (5) patients (Cohort 2) will receive six (6) once-weekly 2-hour IV infusions of SANGUINATE also at a dose of 320 mg/kg. Each patient will be contacted by telephone approximately 24 hours after dosing to verify the safety status of the patient. One week following the Treatment Phase, patients will return to the study center for a Final Visit where safety assessments will be performed. During the Final Visit, patients will receive standard of care treatment of ulcer. All patients will receive once-weekly Standard of Care (SOC) therapy for SCD leg ulcer for the duration of the study. SOC includes dressing the wound with multi-layer, short stretch, compression bandaging. Non-adherent, medical-grade foam will be used as the wound contact layer and primary dressing.

• Study Type: Interventional
• Enrollment (Actual): 10
• Phase: Phase 2

Contacts and Locations

Study Locations

• Dominican Republic
  • Santo Domingo, Dominican Republic
    • General Hospital Plaza de la Salud
• Panama
  • Marbella, Panama
    • Centro Hemato-Oncologico

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Properly consented patients suffering from Sickle Cell Disease (Hb-SS or Hb- Sβ° genotype) associated Leg ulcer.
• Presence of leg ulcer for at least 4 weeks
• Venous Clinical Severity Score of moderate to severe (defined as ≥12)
• Leg ulcer below the knee

Exclusion Criteria:

• Patient presenting with a clinically & laboratory confirmed bacterial, fungal or acid fast organisms
• Patient has a recent acute complication of Sickle Cell Disease (e.g., pain crisis within 7 days, or acute chest syndrome within 21 days)
• Patient is planning to be pregnant, is pregnant, or is breast-feeding
• Presence of moderate to severe renal insufficiency (CrCl < 30 mL/min) or chronic kidney disease, or of moderate to severe hepatic insufficiency (Child-Pugh class B or C)
• Patients with more than 3 times the upper limit of normal laboratory reference range
• Concurrent or recent prior treatment (within 90 days) with an investigational medication
• Patients currently receiving treatment with hydroxyurea must be on stable dose for at least 30 days
• Receipt of a blood transfusion within 21 days

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: SANGUINATE™ (4-week); This is an Open-label, repeated-dose study. About five patients will be observed for 3 weeks continuing on standard of care therapy (for wound cleaning and bandaging). This will be followed by a 4-week treatment period to include once weekly doses of SANGUINATE provided via two-hour IV infusion. The final week of the study will include another observation period wherein all patients will receive standard of care therapy.	Biological: SANGUINATE; A two-hour infusion provided once a week over a 4-week or 6-week period.
Experimental: SANGUINATE™ (6-week); This is an Open-label, repeated-dose study. About five patients will be observed for 3 weeks continuing on standard of care therapy (for wound cleaning and bandaging). This will be followed by a 6-week treatment period to include once weekly doses of SANGUINATE provided via two-hour IV infusion. The final week of the study will include another observation period wherein all patients will receive standard of care therapy.	Biological: SANGUINATE; A two-hour infusion provided once a week over a 4-week or 6-week period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Safety of treatment as determined by changes in vital signs, electrocardiographic, biochemical, hematological, and urinalysis measures, and reported adverse events	8 or 10 weeks
Change in Sickle Cell Disease leg ulcer wound pain scores as measured by a 10-point scale, relative to non-wound site pain scores	8 or 10 weeks
Rate and extent of leg ulcer wound healing as measured by change in wound surface area	8 or 10 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Changes in leg ulcer wound status as measured by need for debridement (type and quantity of non-viable tissue)		8 or 10 weeks
Changes in leg ulcer wound status as measured by extent of exudate production	Change in quality of life as measured by SF-12 Health Survey (acute version) as well as other indicators of patient comfort and well-being	8 or 10 weeks
Changes in leg ulcer wound status as measured by type and amount of granulation tissue		8 or 10 weeks
Changes in leg ulcer wound status as measured by overall change in leg ulcer wound appearance		8 or 10 weeks
Change in local skin in the region of the leg ulcer as measured by skin appearance (coloration, inflammation, etc.)		8 or 10 weeks
Change in local skin in the region of the leg ulcer as measured by skin temperature (relative to body temperature)		8 or 10 weeks
Improvement in leg ulcer wound severity as measured by Venous Clinical Severity Score (VCSS)		8 or 10 weeks
Change in quality of life, as measured by an SF-12 Health Survey (acute version) as well as other indicators of patient comfort and well-being		8 or 10 weeks

Collaborators and Investigators

• Sponsor: Prolong Pharmaceuticals
• Investigators: Study Director: Hemant Misra, PhD, Prolong Pharma

Study record dates

Study Major Dates

• Study Start (Actual): March 1, 2016
• Primary Completion (Actual): October 1, 2016
• Study Completion (Actual): November 1, 2016

Study Registration Dates

• First Submitted: November 2, 2015
• First Submitted That Met QC Criteria: November 6, 2015
• First Posted (Estimate): November 9, 2015

Study Record Updates

• Last Update Posted (Actual): February 28, 2017
• Last Update Submitted That Met QC Criteria: February 24, 2017
• Last Verified: February 1, 2017

More Information

Terms related to this study

• Keywords: Anemia; Sickle Cell Disease; SCD; QOL; Leg Ulcer; Sickle Cell; Leg; Leg Wound; SANGUINATE; LU; Skin Lesion
• Additional Relevant MeSH Terms: Pathologic Processes; Skin Diseases; Hematologic Diseases; Skin Ulcer; Genetic Diseases, Inborn; Anemia; Anemia, Hemolytic, Congenital; Anemia, Hemolytic; Hemoglobinopathies; Ulcer; Anemia, Sickle Cell; Leg Ulcer
• Other Study ID Numbers: SGSC-009

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO