Topical Erythropoietin Hydrogel Formulation for Diabetic Foot Ulcers

Diabetic Foot Ulcer Clinical Trial

— Remede d'Or  

Official title:

Prospective, Multicenter, Single-blind, Randomized, Controlled Clinical Trial on Safety and Efficacy of a Novel Topical Formulation Containing Erythropoietin for the Treatment of Diabetic Foot Ulcers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02361931
• Other study ID #: 0252-12-RMB
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: March 21, 2016
• Est. completion date: June 12, 2018

Study information

• Verified date: March 2019
• Source: Remedor Biomed Ltd
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Remedor has developed a patented technology (RMD-G1), which comprises erythropoietin (EPO) as the active pharmaceutical ingredient (API) in a carbopol-based hydrogel with an FN matrix. RMD-G1 was designed to maintain EPO stability and activity over long periods and to optimize the administration of EPO onto the wound bed.

RMD-G1 is indicated for treating DFUs in adult patients with diabetes mellitus and aims to accelerate the healing of diabetic foot ulcers. RMD-G1 is an adjunct treatment, and not a substitute for good diabetic wound care, which includes initial debridement, wound cleansing, pressure relief, and infection control. In this trial, RMD-G1 is applied daily onto a clean wound at 0.25g per sq. cm. wound surface. After its application, the wound will be covered with a dressing in order to prevent leakage of the hydrogel and contamination of the wound area.

Description:

Delayed healing of a neuroischaemic diabetic foot ulcer (DFU) has been related to prolonged local inflammatory response, an unstable provisional matrix, increased degradation of the extracellular matrix, lack of growth factors and their receptors that are crucial for healing, fibroblast dysfunction, impaired neovascularization, increased oxidative stress, and cellular apoptosis in the wound bed, all of which collectively hinder re-epithelialisation and wound closure.

Erythropoietin (EPO) is an approved drug which is widely used for treating anaemia. EPO is a well-known glycoprotein hormone, which is primarily produced by the tubular cells of the kidney. EPO is widely known for regulating the red blood cell mass by stimulating differentiation and proliferation of precursor cells and hindering apoptosis of erythroid cells in the bone marrow. Millions of people have received EPO since its market approval by the US Food and Drug Administration in 1989 as a treatment of anaemia in patients with chronic kidney disease and later on as a treatment for chemotherapy-associated anaemia. There is growing evidence that both systemic administration and topical EPO application to skin wounds in animals with experimentally-induced diabetes mellitus (DM) and in patients with DM accelerates the healing of these wounds. This accelerated wound healing is mediated by EPO because it concomitantly suppresses the inflammatory response and apoptosis and stimulates angiogenesis, re-epithelialization, and collagen deposition.

Growing studies in experimental healthy and diabetic animals have demonstrated that systemic or topical treatment with EPO onto acute and chronic wounds and burns is safe and effective. Recently, the molecular mechanisms of EPO action in wound repair have been elucidated. EPO acts on all cutaneous cells that are involved in the wound healing process by promoting cellular differentiation and proliferation, exerting cytoprotective actions, and inhibiting inflammation and apoptosis due to the presence of EPO receptors in these cells [Hamed et al. 2014].

The aim of this multicenter, single-blind, randomized, controlled clinical trial is to evaluate the safety and efficacy of topical RMD-G1 treatment for DFUs. This study is an exploratory proof-of-concept study on RMD-G1 treatment for DFU.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: June 12, 2018
• Est. primary completion date: June 11, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

Patients must satisfy all of the following inclusion criteria to be included in the study:

1. Male or female over the age of 18;

2. Diabetes Mellitus type 2;

3. Have a single non-infected Diabetic Hard-to-Heal wound (ulcers/foot ulcers), Wagner grade I or II documented for at least 4 weeks that has not shown signs of healing despite standard treatment;

4. 2 sq.cm. = Wound area at start of treatment = 10 sq.cm.;

5. At least moderate blood perfusion into the affected limb as defined by Ankle Brachial Index (ABI) of >0.4 or if ABI >1.3 then toe pressure > 50 mmHg;

6. Undergo a current physical examination, which reveals no clinically significant abnormalities, except diabetes or diabetic ulcer/wound related condition;

7. Be available for the entire study period, and be able and willing to adhere to protocol requirements;

8. Provide written informed consent prior to admission into the study;

9. no surgical revascularization of the limb with the DFU was done in the previous two months.

Exclusion Criteria:

Patients will be excluded from the study if they meet any of the following exclusion criteria:

1. Diabetes Mellitus non Type 2;

2. Have a glycosylated haemoglobin (HbA1c) >10.0%;

3. Have a body mass index (BMI) > 40 Kg/m2;

4. Have visible bone exposure at wound site;

5. Subjects whose study ulcer size decreases by more than 30% during this initial standard-of-care phase (pre-treatment phase);

6. Have any signs of infection in the wound (which could be linked to raised body temperature), abscess, cellulitis, necrosis, erythema, mild drainage or known osteomyelitis;

7. Have a history of HIV or a clinically significant cardiac, gastrointestinal, endocrine, neurological, liver, or kidney disease;

8. Anemia (Hemoglobin < 9 g/dL) or White Blood Cells count > 11,000/µL or Platelets count < 100,000/µL or liver function tests > 3 times upper normal lab values or Creatinine > 3 mg/dL; any indication of malnourishment (Albumin < 3 g/dL); INR>2 or any other clinically significant blood and urinalysis tests per the physician's discretion

9. Have any clinically significant chronic or acute illness during the 4 weeks prior to admission into the study, except diabetes type2 or during screening period;

10. Patients on concomitant medications that alter blood glucose levels (e.g. ACE inhibitors, lipid lowering agents, etc.) who have not been on a stable dosage regimen for at least 4 weeks prior to entry into the study and who cannot maintain a stable dosage throughout the study;

11. Malignant disease except Basal Cell Carcinoma or Cervical Carcinoma in situ; Chemotherapy treatment or severely immunosuppressed for any reason that would limit or preclude healing in the opinion of the Investigator;

12. Females who are pregnant, lactating, of child-bearing potential, or post-menopausal for less than 2 years, not using a medically approved method of contraception (i.e., oral, transdermal, or implanted contraceptives, intrauterine device, diaphragm, condom, abstinence, or surgical sterility), or females who test positive on a blood-based pregnancy test;

13. Participation in a clinical study or use of an investigational drug within 30 days prior to admission to this study;

14. Residing in a nursing facility and/or are bed-ridden (unable to come to receive treatment at the clinic).

Related Conditions & MeSH terms

• Diabetic Foot
• Diabetic Foot Ulcer
• Foot Ulcer
• Ulcer

Intervention

Drug:
• A hydrogel containing erythropoietin
Standard of wound care, which includes initial debridement, wound cleansing, pressure relief, and infection control. RMD-G1 applied daily onto a clean wound at 0.25g per sq.cm. of wound surface. After its application, the wound is covered with a dressing in order to prevent leakage of the gel and contamination of the wound area.
• Hydrogel (as a part of SOC)
Standard of wound care, which includes initial debridement, wound cleansing, pressure relief, and infection control. Hydrogel applied daily onto a clean wound at 0.25g per sq.cm. of wound surface. After its application, the wound is covered with a dressing in order to prevent leakage of the gel and contamination of the wound area.

Locations

Country	Name	City	State
Israel	HaEmek Medical Center	Afula
Israel	Edith Wolfson Medical Center	H_olon
Israel	Rambam Health Care Campus	Haifa
Israel	Galilee Medical Center	Nahariya
Israel	Poriya Medical Center (a.k.a. Baruch Padeh Medical Center)	Tiberias

Sponsors (1)

Lead Sponsor	Collaborator
Remedor Biomed Ltd

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants without adverse events following RMD-G1 treatment	Absence of serious adverse events associated with the RMD-G1 treatment.	24 weeks
Primary	Number of participants with the reduction of wound area by 75%$ or more	Wound area will be assessed weekly for 75% closure or more of the wound area, which is defined as 75% epithelialization of the wound with no secretions.	12 weeks
Secondary	Number of patients with hypersensitivity at the wound site.	Weekly assessments of wound site for signs of hypersensitivity to the RMD-G1 treatment.	12 weeks
Secondary	Speed of healing	The time to reach complete wound closure (days).	12 weeks
Secondary	Reduction of wound area	Absolute wound area regression (AWAR) (cm2) will be assessed weekly.	12 weeks
Secondary	Partial wound closure	The number of participants with a wound surface area regression = 50% and = 75% by week 4.	4 weeks
Secondary	Rate of wound closure	Mean rate of wound closure (sq. cm./day) will be assessed weekly.	12 weeks
Secondary	Recurrence of closed wounds	Number of wound recurrence cases	24 weeks