Status:
COMPLETED
Subjects With Non-Healing Venous Leg Ulcers Treated With Standard Care Plus Cryopreserved Human Umbilical Cord (TTAX01)
Lead Sponsor:
BioTissue Holdings, Inc
Conditions:
Venous Leg Ulcer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
It is hypothesized that application at 4-week intervals of the human umbilical cord tissue TTAX01 to the surface of a well debrided, nonhealing venous leg ulcer (VLU) will result in a high proportion ...
Eligibility Criteria
Inclusion
- Provide informed consent.
- Age ≥ 18 years and of either sex.
- Willing to comply with protocol instructions, including allowing all study assessments.
- Have a venous leg ulcer (VLU) between the knee and ankle (at or above the malleolus), with a surface area in the range of ≥ 2.0 cm2 and ≤ 18.0 cm2 confirmed using the wound imaging and measurement device.
- Venous insufficiency confirmed by duplex Doppler ultrasound examination for valvular or venous incompetence.
- Arterial supply adequacy confirmed by any one of the following: Great toe pressure ≥ 50 mm/Hg; Systolic blood pressure Ankle Brachial Index (ABI) in the range ≥ to 0.8 to ≤ 1.1; TcPO2 ≥ to 40 mmHg from the foot
- Target ulcer involves a full thickness skin loss, but WITHOUT exposure of tendon, muscle, or bone
- Target ulcer duration ≥ 6 weeks but ≤ 104 weeks
- For diabetic subjects an HbA1C \< 12.0% per the local lab report
Exclusion
- Therapy with another investigational agent within thirty (30) days of Screening, or during the study.
- A target ulcer of non-venous etiologies (e.g., sickle cell anemia, necrobiosis lipoidica diabeticorum, pyoderma gangrenosum, vasculopathic or vasculitic).
- Deep Vein Thrombosis (DVT) that is acute, defined as the first 10 days from onset of symptoms, or any DVT for which compression bandaging is considered by the Investigator to be contraindicated.
- Clinical evidence of ulcer bed infection as described in the Study Guide.
- Documented history of osteomyelitis at the target wound location within 6 months preceding the Screening Visit.
- Refusal of or inability to tolerate compression therapy.
- The subject is pregnant
- The subject is a nursing mother
- The subject is a woman of child-bearing potential who is unwilling to avoid pregnancy or use an appropriate form of birth control (adequate birth control methods are defined as: topical, oral, implantable, or injectable contraceptives; spermicide in conjunction with a barrier such as a condom or diaphragm; IUD; or surgical sterilization of partner).
- Therapy of the target ulcer with other birth tissue products, autologous skin graft, Apligraf®, or Dermagraft® within 30 days preceding the Screening Visit.
- Therapy of the target ulcer with topical growth factors within 1 week preceding the Screening Visit.
- Current therapy with systemic antibiotics.
- Current systemic therapy with cytotoxic drugs.
- Current therapy with chronic (\> 10 days) oral corticosteroids.
- Current therapy with TNF alpha inhibitors other than Trental® (pentoxifylline).
- History of cancer in the preceding 5 years (other than carcinoma in situ of the cervix or adequately treated non-melanoma skin cancers).
- The subject has had previous use of NEOX® CORD 1K®, CLARIX® CORD 1K®, or TTAX01 applied to the index ulcer
- The subject has an allergy to Amphotericin B or glycerol
- The subject has an allergy to primary or secondary dressing materials used in this trial
- Per Investigator's discretion the subject is not appropriate for inclusion in the trial, e.g., undergoing surgical treatments or the subject currently has sepsis, i.e., life-threatening organ dysfunction caused by a dysregulated host response to infection
Key Trial Info
Start Date :
February 14 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 28 2020
Estimated Enrollment :
31 Patients enrolled
Trial Details
Trial ID
NCT03818828
Start Date
February 14 2019
End Date
January 28 2020
Last Update
September 3 2020
Active Locations (6)
Enter a location and click search to find clinical trials sorted by distance.
1
ILD Consulting, Inc.
Carlsbad, California, United States, 92009
2
UCLA Olive View
Sylmar, California, United States, 91342
3
Rosalind Franklin University
North Chicago, Illinois, United States, 60064
4
Advanced Foot & Ankle Center
Las Vegas, Nevada, United States, 89119