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Completed

NCT Number: NCT00798005

Efficacy and Safety Study of NV1FGF in Patients With Severe Peripheral Artery Occlusive Disease.

Peripheral Arterial Occlusive Disease (PAOD) is a condition caused by ischemia in the legs due to atherosclerotic disease affecting the larger arteries of the legs. Chronic PAOD can be regarded as a marker of generalized atherosclerosis. PAOD threatens the survival of an extremity and often causes lifelong disablement from a painful leg. The clinical consequences of PAOD include pain on walking (claudication), pain at rest and loss of tissue integrity in the distal limbs.A variety of medical therapies have been investigated for patients with PAOD. There is currently no evidence to suggest that any medical therapy is effective for patients with rest pain and/or ischemic ulcers.

Also, the use of intramuscular angiogenic VEGF-A gene transfer has recently demonstrated a improvement in clinical and hemodynamic status in patients with severe PAOD

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Key information

Conditions

Severe Peripheral Artery Occlusive Disease Peripheral Arterial Occlusive Disease 1

Age range

45 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Sanofi-Aventis Administrative Office

Bridgewater, New Jersey, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent was to be signed before proceeding with any study procedure.
  • Patients with severe PAD.
  • Trophic lesions with no signs of healing (no reduction in ulcer size or depth) for at least 2 weeks prior to first study treatment administration (Day 1).
  • Patients with objective evidence of peripheral vascular disease in the diseased limb on 2 consecutive examinations performed at least 1 week apart.
  • Demonstration or documentation of total occlusion of the affected limb of one or more of the iliac, superficial femoral, popliteal and/or one or more infrapopliteal arteries as assessed by angiography or magnetic resonance angiography (MRA)
  • Transcutaneous oxygen pressure (TcPO2): mean resting supine TcPO2 of the foot of ≤40 mmHg based on 2 separate measures performed at least 1 week apart
  • Poor/not candidates for revascularization

Exclusion criteria

  • Previous or current history of malignant disease.
  • Positive cancer screening (liver, prostate, colon, cervix, breast, lung)
  • Successful lower extremity surgery (bypass/angioplasty of the leg to be treated) within 3 months prior to the first administration of study treatment [Day 1]).
  • Patients planned to undergo amputation of target limb within 1 month following the first administration of study treatment.
  • Patients with a history of severe renal failure.
  • Creatinine >2.0 mg/dL (176 µmol/L) or estimated creatinine clearance <30 mL.
  • Serious concomitant medical conditions not adequately controlled (other than severe PAD),
  • Buerger's disease.
  • Patients in dialysis.
  • Active proliferative retinopathy
  • Patients who had a stroke or neurologic deficit presumed to be due to stroke within 3 months prior to the first administration of study treatment.
  • Previous treatment with any angiogenic growth factor.
  • Positive serology for HIV 1 or 2.
  • Participation in clinical trials of non-approved experimental agents within 4 weeks before study entry.

Treatment and study plan

XRP0038 (NV1FGF)

Drug

Primary outcomes

  1. evaluate the efficacy and the safety of NV1FGF compared to placebo in patients with severe PAOD.

Secondary outcomes

  1. evaluate the biodistribution of NV1FGF and to measure serum levels of antibodies against FGF-1

Sponsors and collaborators

Lead sponsor

Sanofi

Industry

Registry information

Official study title

A Phase II, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Efficacy and Safety Study of Different Doses and Schedules of Administration of NV1FGF in Patients With Severe Peripheral Artery Occlusive Disease.

Acronym: TALISMAN202

Important dates

Study start
2002
Primary completion
2005
Study completion
2005
First posted
Nov 25, 2008
Registry last updated
Jun 8, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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