ACPs in Severe PAD/CLI by Direct Intramuscular Injection - Full Text View

Purpose

Study title: A Study of Blood-Borne Autologous Angiogenic Cell Precursors Therapy in Patients with Critical Limb Ischemia ( ACPs-CLI )

Principle Investigator: Assoc.Prof. Pramook Mutirangura,M.D. Head of Division of Vascular Surgery , Department of Surgery, Faculty of Medicine Siriraj Hospital , Mahidol University, BKK,Thailand

Study objective : To determine the safety and efficacy of intramuscular injection of blood-borne autologous ACPs in relieving symptoms of critical limb ischemia of patients treated with maximal medical therapy and don't have intravascular or operative revascularization option.

Study Design : A pilot study , a single center, a non-randomized, open-label trial.

Total expected no. of patients : 6 main selection criteria : A. Subjects will have one or more clinical indications diagnostic of CLI such as: distal extremity pain at rest that requires the subject to use analgesics for >2 weeks; or peripheral ischemic ulcer(s); or areas of gangrene ; or non-healing ischemic ulcers AND

B. Subjects will have one or more of the following hemodynamic indicators of severe peripheral arterial occlusive disease:

I. Ankle brachial index < 0.45 II. Toe brachial index < 0.35 III. TcPO2 / TcO2 of < 40 mmHg. C. The subject is a poor candidate for standard revascularization treatment for peripheral arterial disease, based on inadequate bypass conduit, or unfavorable anatomy D. Age 18 to 80 years

Investigational Product : At D-8 250 ml of blood drawn from the patients for production of autologous EPCs or ACPs (VescellTM). On D0 ,at least 1.5 million ACPs with viability >75 % suspended in 30 ml sterile cell culture medium will be injected 1.5 cm deep and 1.5 apart by a 23 -gauge needle into the gastrocnemius muscle of the leg chosen (ischemic leg) for treatment. For injection planning a grid of 10X10 cm will be prepared and in each point 1 ml of ACPs suspension will be injected.

The study consists of 4 periods: Screening ( D-14 to-9& D-8,Treatment(D0),Acute Safety follow-up (D1&D2),Chronic follow-up (D30 & D90)period ,total follow-up of each case is 3 months.

Evaluation criteria :

Safety : no.& duration of adverse event & serious adverse event Efficacy :Attenuate CLI patients symptoms (Rest pain,Pain-free walking distance,Ulcer size &Gangrene dimension and intensity)

Condition	Intervention	Phase
Peripheral Arterial Disease Critical Limb Ischemia	Procedure: Angiogenic Cell Precursors (ACPs) or Vescell TM	Phase I

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study

Official Title:	A Study of Blood-Borne Autologous Angiogenic Cells Precursors Therapy in Patients With Critical Limb Ischemia

Further study details as provided by TheraVitae Ltd.:

Primary Outcome Measures:

Safety [ Time Frame: 3 months ]
Evaluate the safety of ACPs intramuscular injection [ Time Frame: 3 months ]
Efficacy [ Time Frame: 3 months ]
Attenuate CLI patients symptoms as [ Time Frame: 3 months ]
Rest pain [ Time Frame: 3 months ]
Pain-free walking distance [ Time Frame: 3 months ]
Ulcer size [ Time Frame: 3 months ]
Gangrene dimension and intensity [ Time Frame: 3 months ]
Obtain evidence for improvement of tissue perfusion due to ACPs injection [ Time Frame: 3 months ]

Secondary Outcome Measures:

Reduction of CLI patients hospitalization time. [ Time Frame: 3 months ]
Decrease CLI patient amputation rate. [ Time Frame: 3 months ]

Enrollment:	6
Study Start Date:	January 2006
Study Completion Date:	March 2007

Detailed Description:

Six patients with Critical Limb Ischemia (CLI) or severe Peripheral Arterial Disease(PAD) will be enrolled, screened, treated with an injection of Blood-Borne Autologous Angiogenic Cell Precursors(ACPs) in to gastrocnemius of the ischemic leg by intramuscular under regional anesthesia. Following injection.

Eligibility

Ages Eligible for Study:	18 Years to 80 Years
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Subjects will have one or more clinical indications diagnostic of CLI such as: distal extremity pain at rest that requires the subject to use analgesics for >2 weeks; or peripheral ischemic ulcer(s); or areas of gangrene ; or non-healing ischemic ulcers AND
Subjects will have one or more of the following hemodynamic indicators of severe peripheral arterial occlusive disease:
- Ankle brachial index < 0.45
- Toe brachial index < 0.35
- TcPO2 / TcO2 of < 40 mmHg.
The subject is a poor candidate for standard revascularization treatment options for peripheral arterial disease, based on inadequate bypass conduit, or unfavorable anatomy
Age 18 to 80 years
Male or non-pregnant, non-lactating female
Informed consent obtained and consent form signed

Exclusion Criteria:

Patient having on angiography a meaningful supra popliteal occlusion that may relate to symptoms of CLI.
Subjects, who in the opinion of the investigator, have a vascular disease prognosis that indicates they would require a major amputation (at or above the ankle) within 4 weeks of start of treatment
Patient who received blood transfusions during the previous 4 weeks (to exclude the potential of non-autologous ACPs in the harvested blood).
Inability to communicate (that may interfere with the clinical evaluation of the patient)
Major operation during the preceding 3 months
Myocardial infarction or brain infarction or uncontrolled myocardial ischemia or persistent severe heart failure (EF< 25 %) during the preceding 3 months
Significant valvular disease or after valve replacement during the preceding 3 months
After heart transplantation
Severe cardiomyopathy (EF < 25 %)
Renal failure (creatinine > 2 mg/dl )
Hepatic failure
Anemia (lower than 11mg/dl.hemoglobin for female and lower than 12 mg/dl for male)
Abnormal coagulation tests [platelets, PT (INR), PTT]
Stroke within the preceding 3 years
Malignancy within the preceding 3 years
Concurrent chronic or acute infectious disease
Severe concurrent medical disease (e.g., septicemia, HIV-1,2/HBV/HCV infections, poorly controlled insulin-dependent diabetes mellitus ; HBA1c >8 % and proliferative retinopathy , systemic lupus erythematosus, multiple sclerosis, amyotrophic lateral sclerosis)
Chronic immunomodulating or cytotoxic drugs treatment
Patients who have rectal temp. above 38.40C for 2 consecutive days
Patient unlikely to be available for follow-up

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00523731

Locations


Israel, P.O.B.4049,Ness Ziona
	Dr. Valentin Fulga
	Tel viv, P.O.B.4049,Ness Ziona, Israel, 74410

Sponsors and Collaborators

TheraVitae Ltd.

Investigators


Principal Investigator:	Pramook Mutirangura, M.D.	Vascular Surgery Unit,Department of Surgery,Faculty of Medicine Siriraj Hospital,Mahidol University,BKK,Thailand

More Information

Study ID Numbers:	TV-003, ACPs-CLI
First Received:	August 30, 2007
Last Updated:	August 30, 2007
ClinicalTrials.gov Identifier:	NCT00523731
Health Authority:	Thailand: Food and Drug Administration

Keywords provided by TheraVitae Ltd.:

Stem cells

Rest pain

claudication

chronic ischemic or non-healing ulcers

Angiogenesis

no-option cases

Study placed in the following topic categories:

Peripheral Vascular Diseases

Ulcer

Vascular Diseases

Pain

Ischemia

Additional relevant MeSH terms:

Pathologic Processes

Cardiovascular Diseases

ClinicalTrials.gov processed this record on October 10, 2008

Sponsored by:	TheraVitae Ltd.
Information provided by:	TheraVitae Ltd.
ClinicalTrials.gov Identifier:	NCT00523731