CHF6467 SAD and MAD in Patients With Diabetic Foot Ulcer

A Randomised, Double-blind, Placebo-controlled Study to Investigate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Profiles of CHF6467 After Single and Repeated Ascending Doses in Subjects With Diabetic Neurophatic Foot Ulcers (DFU).

To assess the safety and tolerability of single and multiple days' topical dosing with CHF6467 in subjects with diabetic foot ulcer (DFU).

Study Overview

• Status: Completed
• Conditions: Diabetic Neuropathic Foot Ulcers
• Intervention / Treatment: Biological: CHF6467 active

Detailed Description

This first in human study is designed to investigate the tolerability, safety, pharmacokinetics and preliminarily pharmacodynamics following topical administration of single and multiple ascending doses of CHF6467 in subjects diagnosed with diabetic foot ulcer (DFU).

• Study Type: Interventional
• Enrollment (Actual): 93
• Phase: Phase 2; Phase 1

Contacts and Locations

Study Locations

• Bulgaria
  • Sofia, Bulgaria, 1618
    • Comac Medical Ltd.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Subject's written informed consent obtained prior to any study-related procedure;
2. Male or female subject, aged 18 - 80 years (extremes inclusive), diagnosed with Type I or Type II diabetes mellitus, with glycosylated haemoglobin (HbA1c) ≤ 10%.

3. Female subjects of non-childbearing potential (WONCBP):

   • they must report surgical sterilization (performed at least 6 months prior to screening), or
   • menopause (must have had no regular menstrual bleeding for at least one year prior to screening, age ≥ 45 years and FSH at screening ≥ 40 mIU/ml).

4. Female subject with childbearing potential (WOCBP): they must be using one or more of the following reliable methods of contraception during the study period and at least within 90 days after the last study drug administration:

   1. Placement of an intrauterine device (IUD) or intrauterine system (IUS).
   2. Hormonal contraception (implantable, patch, oral).
   3. Barrier methods of contraception: condom or occlusive cap (diaphragm or cervical vaults/caps) with spermicidal foam/gel/film/cream/suppository.
   4. Male Partner sterilization (with the appropriate post-vasectomy documentation of the absence of sperm in the ejaculate).
5. Male subjects; they must be using two effective methods of contraception during the entire study period and not donate sperm within 90 days after the last study drug administration.

6. Presence of at least one diabetic foot ulcer meeting the following criteria:

   1. Diagnosed as a full-thickness, neuropathic DFU, located at or distal to the malleolus (excluding ulcers between the toes but including those of the heel)

   2. SAD: Present for 6 weeks to 12 months, and of 3 - 5 cm2 in area following sharp debridement, confirmed at screening.

      MAD: Present for 6 weeks to 12 months, and of 3 - 6 cm2 in area following sharp debridement confirmed at screening, and of 2-5 cm2 after the 2 weeks run-in period with an area reduction compared to screening <50%.

   3. A minimum 1 cm margin between the qualifying study ulcer and any other ulcers on the specified foot.
   4. SAD: Ulcer must have a depth ≥ 5 mm at some point in its area and be graded 1A according to "The University of Texas Staging System for Diabetic Foot Ulcers" (22), with no capsule, tendon or bone exposed and no tunnelling, undermining, or sinus tracts, after the initial sharp debridement, confirmed at screening.

   MAD: Ulcer must have a depth ≥ 5 mm at some point in its area and be graded 1A or 2A according to "The University of Texas Staging System for Diabetic Foot Ulcers" (22), after the initial sharp debridement, confirmed at screening.

7. Subject must be able to hold the target ulcer in such a position and orientation that the study medication can be applied without significant loss of substance through run-off, until the dressing has been applied.

8. Adequate vascular perfusion of the affected limb demonstrated within 30 days prior to screening, as defined by at least one of the following:

   1. Ankle-Brachial Index (ABI) ≥ 0.9 and ≤ 1.2, confirmed by transcutaneous oxygen partial pressure (TcPO2) >50 mmHg
   2. Toe pressure (plethysmography) >50 mmHg
   3. Doppler ultrasound (biphasic or triphasic waveforms) at least on two vessels at the ankle consistent with adequate blood flow to the affected extremity, as determined by SoC.

Exclusion Criteria:

1. For females only: pregnant or lactating female subject, confirmed by a positive serum pregnancy test at screening and a urine test performed on Day -1.

2. Subject with:

   1. Ulcer(s) accompanied by infected cellulitis, osteomyelitis, or clinical signs or symptoms of infection confirmed by a cultural exam made on the material taken off from the ulcer according to the technique described in the guidelines for diagnosis and management of diabetic foot infections of the Infectious Diseases Society of the Americas (IDSA) (19).
   2. Gangrene or necrosis on any part of the affected limb.
   3. Active or chronic Charcot's foot on the study limb.
   4. Planned vascular surgery, angioplasty or thrombolysis or previous revascularization procedure performed within 1 month prior to enrolment.
   5. SD only: Ulcers involving exposure of tendon, bone, or joint capsule (It is acceptable to have ulcers extending through the dermis and into subcutaneous tissue with presence of granulation tissue).
   6. Ulcer(s) of non-diabetic aetiology.
   7. Previous Lisfranc or Chopart's amputations on the same target foot.
   8. Actual or recent (3 weeks) antibiotic therapy for any reason.
   9. Bedridden subjects or subjects with a life expectancy less than one year.
3. Use of any growth factor therapy in the 3 months prior to screening.
4. History of malignancy in the 5 years prior to screening or those with a strong family history of cancer (e.g. familial cancer disorders), with the exception of squamous cell or basal cell carcinoma of the skin that has been definitively treated.
5. Clinically significant cardiovascular, pulmonary, renal, endocrine, hepatic, neurological, psychiatric, immunological, gastrointestinal, haematological or metabolic disease that is, in the opinion of the Investigator, not stabilised or may otherwise impact subject safety or study results (in cases of doubt, the Sponsor's Clinical Research Physician should be consulted).
6. Subject undergoing haemodialysis or peritoneal dialysis or with chronic renal insufficiency (plasma creatinine > 2 mg/dl).
7. Subject with significantly abnormal key laboratory parameters interfering with the safety of the patient according to the PI judgement.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

6

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: SAD - Cohort A - CHF6467 0.3 µg/mm2; Cohort A: will be administered with CHF6467 0.3 µg/mm2 ulcer area as single dose.	Biological: CHF6467 active; CHF6467, is mutated form of the human Nerve Growth Factor (NGF).
Experimental: SAD - Cohort B - CHF6467 1 µg/mm2; Cohort B: will be administered with 1 µg/mm2 ulcer area as single dose.	Biological: CHF6467 active; CHF6467, is mutated form of the human Nerve Growth Factor (NGF).
Experimental: SAD - Cohort C - CHF6467 3 µg/mm2; Cohort C: will be administered with 3 µg/mm2 ulcer area as single dose.	Biological: CHF6467 active; CHF6467, is mutated form of the human Nerve Growth Factor (NGF).
Experimental: SAD - Cohort D - CHF6467 6 µg/mm2; Cohort D: will be administered with 6 µg/mm2 ulcer area as single dose.	Biological: CHF6467 active; CHF6467, is mutated form of the human Nerve Growth Factor (NGF).
Experimental: MAD - Cohort E - CHF6467 0.3 or 1 µg/mm2; Cohort E: will be administered with 0.3 or 1 µg/mm2 ulcer area (total daily dose) as multiple dose (14 days). The dose will be selected based on the SAD results.	Biological: CHF6467 active; CHF6467, is mutated form of the human Nerve Growth Factor (NGF).
Experimental: MAD - Cohort F - CHF6467 1 or 3 µg/mm2; Cohort F: will be administered with 1 or 3 µg/mm2 ulcer area (total daily dose) as multiple dose (14 days). The dose will be selected based on the SAD results.	Biological: CHF6467 active; CHF6467, is mutated form of the human Nerve Growth Factor (NGF).

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Treatment Emergent Adverse Events (TEAEs)	During the SAD and the MAD, the number of events and the number and percentage of subjects experiencing TEAEs, treatment emergent ADRs, serious TEAEs, non-serious TEAEs, severe TEAEs, TEAEs leading to discontinuation of study drug and TEAEs leading to death will be presented by treatment.	SAD: From Day 1 up to Day 28; MAD: From Day 1 up to Day 84;

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pharmacokinetics: AUC0-72h after single administration	During the SAD: Dose proportionality of CHF6467 for AUC0-72h, and classical PK parameters will be calculated	SAD: Serial of timepoints until 72 hours post dose
Pharmacodynamic: Ulcer area after multiple administration	MAD: Ulcer area measurements expressend in cm2 over time after multiple administration	MAD: From Day 1 to Days 4, 7, 10, 14, 17, 21, 24, 28, 31, 35, 38, 42, 45, 49, 52, 56, 59, 63, 66, 70, 73, 77, 80 and 84
Pharmacokinetics: AUC0 to infinit after multiple administration	During the MAD: Dose proportionality of CHF6467 for AUC 0 to infinit, and classical PK parameters will be calculated	MAD: Serial of timepoints at Day 1, Day 2, Day 4, Day 7, Day 10, Day 13, Day 14, Day 21 and Day 28

Collaborators and Investigators

• Sponsor: Chiesi Farmaceutici S.p.A.
• Collaborators: Comac Medical
• Investigators: Principal Investigator: Iliya Lozev, MD, Comac Medical

Publications and helpful links

Helpful Links

• Study Record on EU Clinical Trials Register including results
• Lay Summaries of study results available in the CHIESI Clinical Study Register

Study record dates

Study Major Dates

• Study Start (Actual): October 17, 2018
• Primary Completion (Actual): January 7, 2021
• Study Completion (Actual): January 7, 2021

Study Registration Dates

• First Submitted: March 28, 2019
• First Submitted That Met QC Criteria: September 3, 2019
• First Posted (Actual): September 4, 2019

Study Record Updates

• Last Update Posted (Actual): February 23, 2022
• Last Update Submitted That Met QC Criteria: February 7, 2022
• Last Verified: February 1, 2022

More Information

Terms related to this study

• Keywords: DFU; Diabetic Foot Ulcers; Diabetic Neuropathic Foot Ulcers
• Additional Relevant MeSH Terms: Pathologic Processes; Skin Diseases; Leg Ulcer; Skin Ulcer; Foot Diseases; Foot Ulcer; Ulcer
• Other Study ID Numbers: CLI-06467AA1-01; 2018-001724-19 (EudraCT Number)

Plan for Individual participant data (IPD)

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

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No