Safety, Tolerability and Efficacy of CYP-006TK in Adults With Diabetic Foot Ulcers

Sponsor
Cynata Therapeutics Limited (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05165628
Collaborator
(none)
30
1
2
10.9
2.8

Study Details

Study Description

Brief Summary

Design: A randomised, controlled, prospective trial. Participants will be patients with non-healing diabetic foot ulcers.

The study will aim to recruit 15 participants per study group (30 participants in total).

Participants will be randomly allocated to one of two treatment groups:
  • Group 1: CYP-006TK

  • Group 2: Standard care This will be an open label study with respect to treatment allocation. However, the person reviewing images of the study ulcers to assess healing will be blind to the participant's treatment allocation.

Participants assigned to Group 1 will be treated with CYP-0006TK dressings on 8 occasions over 4 weeks. The dressings will be changed every 3 or 4 days. After the first 4 weeks, participants in Group 1 will revert to standard care for the rest of the study. Participants assigned to Group 2 will have their ulcer treated with standard care throughout the study.

Participants will attend a total of 16 scheduled visits over 24 weeks. There will be a mixture of on-site (hospital/clinic) visits, and home visits. The study will end 24 weeks after the initiation of treatment, unless the study ulcer is completely headed before then.

Condition or Disease Intervention/Treatment Phase
  • Combination Product: CYP-006TK
Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Randomised, Controlled, Phase 1 Study to Investigate Safety, Tolerability and Efficacy of CYP-006TK in Adults With Diabetic Foot Ulcers
Actual Study Start Date :
Jan 4, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group 1 - CYP-006TK

Participants will receive CYP-006TK dressings

Combination Product: CYP-006TK
CYP-006TK is allogenic mesenchymoangioblast-derived mesenchymal stem cells (MCA-derived MSCs) or Cymerus™ MSCs, seeded onto a heptylamine plasma polymer-coated silicone dressing

No Intervention: Group 2 - Standard of Care

Participants will continue to be treated as per local standard of care

Outcome Measures

Primary Outcome Measures

  1. Incidence and severity of treatment-emergent adverse events (TEAEs) [24 weeks]

  2. Incidence of changes from baseline in haematology, biochemistry, and urinalysis parameters. [24 weeks]

    Results will be summarised by individual and by treatment group using descriptive statistics.

Secondary Outcome Measures

  1. Percentage of area change of study ulcer from baseline to weeks 12 and 24 [12 and 24 weeks]

  2. Number of days to complete ulcer healing [12 and 24 weeks]

  3. Number of days to 50% ulcer healing [12 and 24 weeks]

  4. Percentage change in ulcer volume from baseline to weeks 12 and 24 [12 and 24 weeks]

  5. Changes from baseline in ulcer pain assessed using a Numeric Rating Scale [12 and 24 weeks]

  6. Number clinic/home care visits across groups [12 and 24 weeks]

  7. Differences across groups on ulcer dressing products used [12 and 24 weeks]

  8. Changes from baseline in Quality of Life assessed using the Cardiff Wound Impact Schedule [12 and 24 weeks]

  9. Duration of clinic/home care visits across groups [12 and 24 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Adults at least 18 years of age up to 80 years of age, inclusive.

  2. Have a current diagnosis of diabetes mellitus (DM)

  3. With at least one non-healing cutaneous ulcer on the foot or the lower legs

  4. With ankle brachial index (ABI) ≥ 0.4 and/or toe pressure >30 mmHg on the limb with the study ulcer.

  5. Participant co-morbidities are adequately managed, and the participant has a life expectancy of at least 6 months as determined by the Investigator based on medical history, physical examination, vital signs, or clinical laboratory tests, etc.

  6. A negative pregnancy test, (i.e. for female participants with childbearing potential).

  7. Willing to comply with birth control measures, to prevent female participants becoming pregnant for six months following administration of the study treatment.

  8. Able to follow the Investigator's instruction on ulcer care (in the opinion of the Investigator).

  9. Agrees to provide written informed consent.

Exclusion Criteria:
  1. Planned vascular surgery, angioplasty, thrombolysis or amputation of the affected limb in the next six months.

  2. Pregnant or breastfeeding.

  3. Active infection in the study ulcer.

  4. Any sign of osteomyelitis associated with the study ulcer.

  5. Study ulcer extends to bone or periosteum (ulcers that reach a ligament, joint capsule, fascia, or tendon are not excluded).

  6. Known autoimmune disease other than diabetes, including but not limited to lupus erythematosus, multiple sclerosis.

  7. Treatment with systemic immunosuppressants within 90 days of screening.

  8. Active malignancy or history of malignancy within five years prior to screening (with the exception of a past history of basal or squamous cell carcinomas).

  9. Serum GGT, AST or ALT > 5 × upper limit of the normal range (ULN).

  10. . Known history of HIV infection

  11. Prior administration of any cell-based treatment to the limb affected by the study ulcer.

  12. Received any investigational research agent within 60 days or within five half-lives of the last treatment (if the half-life of the investigational agent is known to be longer than 12 days) prior to the planned initiation of study treatment.

  13. Any other medical condition or laboratory abnormality judged as clinically significant by the Investigator or study Medical Monitor which could confound the evaluation of the trial treatment.

  14. With history of sensitivity to materials of bovine, porcine origin, or human serum albumin.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Central Adelaide Local Health Network Adelaide South Australia Australia 5000

Sponsors and Collaborators

  • Cynata Therapeutics Limited

Investigators

  • Study Director: Jolanta Airey, MD, Cynata Therapeutics Limited

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cynata Therapeutics Limited
ClinicalTrials.gov Identifier:
NCT05165628
Other Study ID Numbers:
  • CYP-DFU-P1-01
First Posted:
Dec 21, 2021
Last Update Posted:
Mar 22, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2022