A Dose Finding Study of Topically Applied I-020201 as an Adjunct to Good Standard-of-care in Patients With Chronic Diabetic Foot Ulcers (DFU)


Tracking Information

Start Date  ICMJEMay 2009
Estimated Primary Completion DateDecember 2010   (final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE 
 (submitted: June 5, 2009)
Percentage reduction in ulcer surface area [ Time Frame: 4 weeks after treatment start ] [ Designated as safety issue: No ]
Original Primary Outcome Measures  ICMJESame as current
Change HistoryComplete list of historical versions of study NCT00915486 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE 
 (submitted: June 5, 2009)
  • Incidence of complete wound closure (full re-epithelialization with confirmation 4 weeks afterwards) [ Time Frame: At 12 and 16 weeks after treatment start ] [ Designated as safety issue: No ]
  • Incidence of complete wound closure (full re-epithelialization with confirmation 4 weeks afterwards) [ Time Frame: Within the whole study period (28 weeks after treatment start) ] [ Designated as safety issue: No ]
  • Time to complete wound closure (full re-epithelialization with confirmation 4 weeks afterwards). [ Time Frame: At any time during the study ] [ Designated as safety issue: No ]
  • Incidence of treatment failure defined as <30% decrease in ulcer size [ Time Frame: After 8 weeks of treatment ] [ Designated as safety issue: No ]
  • Incidence of patients with ulcer recurrence [ Time Frame: Up to 16 and 28 weeks after treatment start ] [ Designated as safety issue: No ]
  • Incidence of treatment-related adverse events (systemic and at the target ulcer) and all AEs/SAEs [ Time Frame: During the whole study period ] [ Designated as safety issue: No ]
  • Changes in systemic PDGF-AB and antibody levels against TG-PDGF.AB and aprotinin [ Time Frame: At 1, 4, 12, 16 and 20 weeks after treatment start ] [ Designated as safety issue: No ]
  • Changes in vital signs, body weight, physical examination and laboratory parameters [ Time Frame: Throughout the study and 28 weeks after treatment start ] [ Designated as safety issue: No ]
Original Secondary Outcome Measures  ICMJESame as current

Descriptive Information

Brief Title  ICMJEA Dose Finding Study of Topically Applied I-020201 as an Adjunct to Good Standard-of-care in Patients With Chronic Diabetic Foot Ulcers
Official Title  ICMJEA Randomized, Multi-center, Controlled, Parallel Group, Dose Finding Study of the Efficacy and Safety of Topically Applied I-020201 as an Adjunct to Good Standard-of-care Versus Good Standard-of-care Alone in Patients With Chronic Diabetic Foot Ulcers
Brief Summary

Although major improvements in the management and treatment of diabetic foot ulcers have been made, the clinical and financial burden of such long-term wounds is still high and is likely to increase as the general population ages. The large population affected by diabetic foot ulcers and the high rates of failure ending with amputation even with the best therapeutic regimens have resulted in the development of new therapies. I-020201 is a bioactive therapy intended for topical treatment of hard-to-heal diabetic foot ulcers, stimulating the granulation tissue formation. This study aims to evaluate the safety and efficacy of I-020201 in adjunct to good standard of care in patients with chronic diabetic foot ulcer.

Detailed Description 
Study PhasePhase II
Study Type  ICMJEInterventional
Study Design  ICMJETreatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Dose Comparison, Parallel Assignment, Safety/Efficacy Study
Condition  ICMJEDiabetic Foot Ulcer
Intervention  ICMJE
  • Procedure: Good Standard of Care (GSoC)
    Procedural treatment twice per week
  • Biological: Vehicle
    Topical fibrin as an adjunct to GSoC twice per week
  • Biological: I-020201
    Topical treatment with 3 different concentrations as an adjunct to GSoC twice per week
Study Arms / Comparison Groups
  • Good Standard of Care (GSoC): Experimental
    Twice per week
    Intervention: Procedure: Good Standard of Care (GSoC)
  • GSoC + vehicle: Experimental
    Twice per week
    Interventions:
    • Procedure: Good Standard of Care (GSoC)
    • Biological: Vehicle
  • GSoC + I-020201 (33microg): Experimental
    Twice per week
    Interventions:
    • Procedure: Good Standard of Care (GSoC)
    • Biological: I-020201
  • GSoC + I-020201 (100microg): Experimental
    Twice per week
    Interventions:
    • Procedure: Good Standard of Care (GSoC)
    • Biological: I-020201
  • GSoC + I-020201 (300microg): Experimental
    Twice per week
    Interventions:
    • Procedure: Good Standard of Care (GSoC)
    • Biological: I-020201

Recruitment Information

Estimated Enrollment  ICMJE210
Estimated Completion DateDecember 2010
Estimated Primary Completion DateDecember 2010   (final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • male or female, aged ≥ 18 years
  • given written informed consent
  • female of childbearing potential with a negative result from the pregnancy test at screening who agrees to use an acceptable birth control method (hormonal or IUD) or abstinence throughout the trial
  • Type 1 or Type 2 Diabetes mellitus with HbA1c < 10%
  • with only one diabetic foot ulcer on the foot to be treated on or below the ankle

Exclusion Criteria:

  • pregnant or breast-feeding
  • known or suspected allergies to any of the components of the I-020201
  • uncontrolled anemia (Hb < 10 g/dL in females and < 12 g/dL in males)
  • hypoalbuminemia (albumin < 3 g/dL)
  • overtly infected target ulcer (as judged by investigator)
  • highly exuding wounds (wounds that require a daily dressing change)
  • osteomyelitis
  • systemic infections
  • acute Charcot foot and severe chronic Charcot deformity
  • ABPI < 0.7 or ankle systolic pressure < 70 mm Hg
  • one of the following findings (only 1 out of 3 tests is required):

    • on Doppler waveform analysis on the dorsalis pedis and posterior tibial arteries a monophasic or biphasic flow (with loss of reverse flow) in either foot artery, or
    • a toe: brachial index < 0.7, or
    • transcutaneous oxygen pressure (TcpO2) < 40 mm Hg
  • suspicion, presence or history of systemic or local cancer or tumor of any kind
GenderBoth
Ages18 Years and older
Accepts Healthy VolunteersNo
Contacts  ICMJE
Contact: Mitra Safari+41 44 200 5600 ext 82mitra.safari@kuros.ch
Location Countries  ICMJECzech Republic,   Germany,   Hungary,   Romania,   Russian Federation,   Serbia

Administrative Information

NCT ID  ICMJENCT00915486
Responsible PartyVirginia Jamieson, Kuros Biosurgery
Study ID Numbers  ICMJECS I-020201/01
Study Sponsor  ICMJEKuros Biosurgery AG
Collaborators  ICMJE 
Investigators  ICMJE 
Information Provided ByKuros Biosurgery AG