Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:19 PM
Ignite Modification Date:
2025-12-24 @ 11:19 PM
NCT ID:
NCT01059656
Eligibility Criteria:
Inclusion Criteria:
* Primitive unresectable DFSP, locally advanced (potentially mutilating surgery), or in relapse or transformed.
* Histologic confirmation of the Darier-FERRAND tumour (transformed types will be accepted provided a previous caryotype confirming the translocation (17,22)
* Age \> or equal to 20 years
* Signed informed consent
* Appropriate contraception
* No evolutive tumoural disease except baso-cellular carcinoma
* Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1.
Exclusion Criteria:
* Patient refusal to participate
* Age \< 20 years
* Pregnant or lactating women
* Other evolutive tumour disease except baso-cellular carcinoma
* Haematologic abnormalities:Hemoglobin \< 9g/dl, PNN \<
* 1500/mm3, Platelets \<100000/mm3
* AST and ALT \> 2N
* Bilirubin \> 1.5N
* Creatinin \> 1.5mg/dL or creatinin clearance \<30ml/mn
* Proteinuria \>1g/24h
* Serum albumin\< 2.5g/dL
* Hepatitis B, C and/or HIV known Infection
* Treatment interfering with pazopanib
* Major surgical procedure, open biopsy, or significant traumatic injury within 4 weeks prior to beginning therapy, or anticipation of the need for a major surgical procedure during the course of the study.
* Clinically significant gastrointestinal abnormalities including, but not limited to:Malabsorption syndromeDisease significantly affecting gastrointestinal function or major resection of the stomach or small bowel that could affect the absorption of study drug.Active peptic ulcer diseaseInflammatory bowel diseaseUlcerative colitis, erosive esophagitis or gastritis, infectious or inflammatory bowel disease, diverticulitis or other gastrointestinal condition increasing the risk of perforation.History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 28 days prior to beginning study treatment· Presence of active or uncontrolled infection.
* Evidence of active bleeding or bleeding diathesis.
* History of any one or more of the following cardiovascular conditions within the past 6 months:Coronary/peripheral artery bypass graft, cardiac angioplasty or stenting.Myocardial infarction.Severe/unstable angina pectoris.Symptomatic peripheral vascular disease pulmonary embolism, thromboembolic event, cerebrovascular accident or transient ischemic attack.Class III or IV congestive heart failure, as defined by the New York Heart Association
* Cardiovascular disease with NYHA \> II
* Poorly controlled hypertension (defined as a systolic blood pressure (SBP) of ≥140 mmHg or diastolic blood pressure (DBP) ≥90 mmHg.
* Following abnormalities on ECG : Q wave, ischemia, QTc \> 450 msec, atrioventricular block 2 or 3, atrial fibrillation
* Therapeutic anticoagulation treatment.
* Chronic daily treatment with aspirin (≥ 100 mg/day) or non-steroidal anti-inflammatory agents known to inhibit platelet function. Treatment with dipyridamole, ticlopidine, clopidogrel and/or cilostazol is also not allowed.. Concurrent treatment with an investigational agent or participation in another clinical trial.
* Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to pazopanib.
* Taken by the order treatment anti cancerous concomitants within 4 weeks previous inclusion
* Radiotherapy on the hurt within 3 months previous inclusion
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Study:
NCT01059656
Study Brief:
Protocol Section:
NCT01059656