BCX-1777 in Treating Patients With Refractory Cancer (NCT00073944) | Clinical Trial Compass
CompletedPhase 1
BCX-1777 in Treating Patients With Refractory Cancer
United StatesStarted 2003-04
Plain-language summary
RATIONALE: BCX-1777 may stop the growth of cancer cells by blocking the enzymes necessary for their growth.
PURPOSE: Phase I trial to study the effectiveness of BCX-1777 in treating patients who have refractory cancer.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
DISEASE CHARACTERISTICS:
* Histologically confirmed diagnosis of 1 of the following:
* Hematologic malignancy that is refractory to at least 1 prior curative treatment
* Non-hematologic tumor that is refractory to at least 2 prior therapies, with or without measurable disease, including the following:
* Gastrointestinal adenocarcinoma of 1 of the following sites:
* Pancreatic
* Biliary
* Gastric
* Colorectal
* Esophageal
* Melanoma
* Ovarian cancer
* Astrocytoma brain tumor
* Not immediately eligible for any other treatment that would be potentially curative or life-prolonging, in the opinion of the investigator
* Patients who may be candidates for future bone marrow transplantation are eligible
* No brain metastases (other than astrocytomas)
* No clinically significant pleural effusion
* No complete tumor obstruction (e.g., bronchus, ureter, or bowel)
PATIENT CHARACTERISTICS:
Age
* 18 and over
Performance status
* ECOG 0-2 OR
* Karnofsky 50-100%
Life expectancy
* Not specified
Hematopoietic
* WBC at least 3,500/mm\^3
* Absolute neutrophil count at least 1,500/mm\^3
* Platelet count greater than 50,000/mm\^3
* Hematocrit stable without the need for transfusion (epoetin alfa support allowed)
Hepatic
* Bilirubin less than 1.5 times upper limit of normal (ULN) (unless due to Gilbert's syndrome)
* SGOT and SGPT less than 2 times ULN
* No active hepatitis B or C
Renal
* Creatinine clearance at least 50 mL/min
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