Over Berrak Hücreli Kanserlerinde ENMD-2076 Çalışması

Sade dilde özet

Bu çalışma, over berrak hücreli karsinomu (ovarian clear cell carcinoma, yumurtalık kanseri) olan hastalarda ENMD-2076 adlı ilacı incelemiştir. Araştırmaya, histolojik olarak doğrulanmış over berrak hücreli kanser tanısı olan, ölçülebilir hastalığı bulunan ve daha önce platin bazlı tedavi almış 18 yaş üzeri hastalar dahil edilmiştir. Çalışma Faz 2 aşamasında yürütülmüş ve tamamlanmıştır.

Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.

Deney bilgileri

Faz

Faz 2 (Phase 2)

Durum

Tamamlandı

Sponsor

University Health Network, Toronto

Müdahale

ENMD-2076

Başlangıç

01.09.2013

Tahmini bitiş

01.01.2017

Ülkeler

Canada

İlgili genler

Merkezler

• Calgary, Canada
• Edmonton, Canada
• Vancouver, Canada
• London, Canada
• Ottawa, Canada
• Toronto, Canada

Uygunluk kriterleri

Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.

Inclusion Criteria:

* Have histologically documented diagnosis of ovarian clear cell carcinoma.
* Any number of prior chemotherapy regimens will be allowed but must include 1 line of platinum based therapy, and may include chemotherapy, biologics or other targeted therapies (except for Aurora A targeted therapies).
* Meet RECIST criteria (version 1.1) within 28 days of start of treatment by having measurable disease defined as one or more lesions that can be accurately measured in one or more dimensions. Areas of previous radiation may not serve as measurable disease unless there is evidence of progression post radiation.
* At time of registration, if the patient has had previous treatment it must have been at least 4 weeks since major surgery or radiation therapy; four weeks from any other previous anti-cancer therapy including biologics. Patients must have recovered from their treatment-related events with the exception of alopecia.
* Are ≥18 years of age
* Have clinically acceptable laboratory screening results within certain limits specified below:

  * AST and ALT ≤ 2.5 times upper limit of normal (ULN) or less than or equal to 5 times ULN if liver metastases are present
  * Total bilirubin ≤ 1.5 x ULN
  * Creatinine ≤ 1.5 x UL
  * Absolute neutrophil count ≥ 1500 cells/mm
  * Platelets ≥ 150,000/mm3
  * Hemoglobin ≥ 9.0 g/dl
* Have an ECOG performance status of ≤ 2
* Women of child-producing potential must agree to use effective contraceptive methods prior to study entry, during study participation, and for at least 30 days after the last administration of study medication. A serum pregnancy test within 72 hours prior to the initiation of therapy will be required for women of childbearing potential.
* Have the ability to understand the requirements of the study, provide written informed consent, abide by the study restrictions, and agree to return for the required assessments.
* Able to tolerate oral medication.

Exclusion Criteria:

* Women who are pregnant or nursing
* Have active, acute, or chronic clinically significant infections or bleeding.
* Have uncontrolled hypertension (systolic blood pressure greater than 150mmHg or diastolic blood pressure greater than 100mmHg); or history of congestive heart failure (equal to or greater than Grade 2).
* Have active angina pectoris, stroke, previous myocardial infarction within the past 12 months and not clinically stable, or any other pre-existing uncontrolled cardiovascular condition.
* Have chronic atrial fibrillation or QTc interval corrected for heart rate of greater than 470 msec.
* Have additional uncontrolled serious medical or psychiatric illness.
* Require therapeutic doses of anti-coagulation with warfarin or other coumarin derivatives. However, treatment with low molecular weight heparin (LMWH) is allowed.
* Known CNS metastases
* Have any medical condition that would impair the administration of oral agents including recurrent bowel obstructions, inflammatory bowel disease or uncontrolled nausea, vomiting or diarrhea
* Have persistent 2+ protein by urinalysis (patients with 2+ proteinuria that have a spot protein:creatinine ratio of less than 0.3 may be enrolled) or a history of nephrotic syndrome
* Have an active or history of additional malignancy which in the opinion of the study doctor would make assessment of outcome difficult.
* Require treatment with drugs known to be potent inducers or inhibitors of CYP3A4 at the time of registration