Tissue Repair Gel in Venous Leg Ulcers (US)
Purpose
The goal of this clinical trial is to learn if TR987 0.1% gel + Standard of Care works better than Standard of Care alone to treat Venous Leg Ulcers (VLUs). It will also provide additional information about the safety of drug TR987 0.1% gel.
Conditions
- Venous Leg Ulcer
- Venous Ulcer
- Venous Stasis Ulcer
- Venous Stasis
- Wound Heal
- Wounds
- Venous Insufficiency of Leg
- Non-healing Wound
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Adults 18 years and older - Venous insufficiency has been clinically diagnosed clinically and medically confirmed. - Females who are neither pregnant nor breastfeeding and if of child-bearing potential are on an acceptable method of birth control. - The Venous Ulcer should be between 2 cm2 and 12 cm2 at randomization. - Target ulcer age must be ≥ 4 weeks at Screening. - Participants must have adequate arterial flow as confirmed by ABI/TBI, TB, SPP, TCPo2, or Duplex Doppler. - Body mass index (BMI) ≤ 50 kg/m2. - HbA1C ≤12%.
Exclusion Criteria
- Target ulcer has been treated with prohibited medications or therapies. - History of radiation at the target ulcer site. - Target ulcer decreases in area by 30% or more during screening period. - History of osteomyelitis at the target ulcer within 6 months of screening. - History of cancer in the preceding 5 years (except as noted in the protocol). - Participants considered nutritionally deficient.
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Intervention Model Description
- This is an outpatient, randomized, parallel- group, double-blind, multicenter, 16-week study with 2 treatment arms: TR987 0.1% gel + Standard of Care and Standard of Care alone in participants who have a non-healing Venous Leg Ulcer (VLU)
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Masking Description
- Participants will be randomized to either TR987 1% gel + Standard of Care and Standard of Care alone. Sponsor, participant, and Investigator/Outcomes Assessor will be masked throughout the treatment period.
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental TR987 0.1% gel + Standard of Care |
Participants will receive up to 16 weeks of TR987 0.1% gel topically + Standard of Care (wound cleansing/dressings and compression bandaging). Treatment will be twice weekly for the first four weeks then weekly for the remaining 12 weeks. |
|
|
Other Standard of Care |
|
Recruiting Locations
Castro Valley 5334928, California 5332921 94546
Los Angeles 5368361, California 5332921 90063
San Francisco 5391959, California 5332921 94115
San Francisco 5391959, California 5332921 94117
Deerfield Beach 4153071, Florida 4155751 33442
Springfield 4250542, Illinois 4896861 62704
Winston-Salem 4499612, North Carolina 4482348 27157
More Details
- NCT ID
- NCT06707090
- Status
- Recruiting
- Sponsor
- TR Therapeutics
Study Contact
Anhthu Nguyen Vice President, Global Clinical Operations(+61) 280 034 554
anhthu.nguyen@trtherapeutics.com
Detailed Description
This is an outpatient, randomized, parallel- group, double-blind, multicenter, 16-week study with 2 treatment arms: TR987 0.1% gel + Standard of Care and Standard of Care alone in participants who have a non-healing Venous Leg Ulcer (VLU). The primary objective is to assess the proportion of participants with Complete Closure of the target ulcer at or before the Week-16 end of treatment (EOT) visit. Secondary endpoints include: • Proportion of participants with Complete Closure of the target ulcer at or before the Week 16 visit AND for whom the ulcer remains closed at the 3-Month Follow-Up visit after such closure (a composite endpoint). • Change from baseline in participant's perception of pain level at 12 weeks. • Percent change from baseline in the target ulcer area at 12 and 16 weeks. In the event of Complete Closure before these time points, the target ulcer area will be deemed to be zero at those time points for purposes of calculation of this endpoint. • Proportion of participants with Complete Closure of the target ulcer at or before the Week 12 treatment visit. • Proportion of participants with any significant reduction in pain at or before 12 weeks. There are also some supplementary and safety endpoints.