Phase I Trial of Oral PX-866

Advanced Solid Tumors Clinical Trial

Official title:

A Phase I Trial of Oral PX-866 (a PI-3K Inhibitor) in Patients With Advanced Solid Tumors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00726583
• Other study ID #: PX-866-001
• Status: Completed
• Phase: Phase 1
• Start date: June 2008
• Est. completion date: September 2011

Study information

• Verified date: October 2011
• Source: Seattle Genetics, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is being conducted to determine the safety and maximally tolerated dose of PX-866 when given orally on two different schedules: daily on days 1-5 and 8-12 of a 28 day cycle and daily on days 1-28 of a 28 day cycle.

Description:

PX-866 is a targeted inhibitor of PI-3K. This study is being conducted to determine the maximally tolerated dose of PX-866 when given orally on two different schedules: daily on days 1-5 and 8-12 of a 28 day cycle and daily on days 1-28 of a 28 day cycle.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 90
• Est. completion date: September 2011
• Est. primary completion date: September 2011
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically or cytologically confirmed diagnosis of advanced solid tumor and has failed or is intolerant of standard therapy, or for whom standard therapy does not exist.

• 18 years of age or older.

• ECOG performance status 0 to 1.

• Predicted life expectancy of at least 12 weeks.

• Discontinued prior chemotherapy or other investigational agents for at least three weeks prior to receiving the first dose of study drug (six weeks for mitomycin C, nitrosureas,vaccines,or antibody therapy)and recovered from the toxic effects of the prior treatment (recovered to baseline or =grade 1 per Common Toxicity Criteria for Adverse Events (CTCAE)).

• Discontinued any radiation therapy for at least four weeks and have recovered from all radiation-related toxicities (recovered to baseline or =CTCAE grade 1) prior to receiving the first dose of study drug. Palliative radiation of 10 fractions or less is permitted and a four week interval is not necessary (also allowed during therapy).

• Adequate hematologic function as defined by the following: WBC count >3,000 cells/µL; platelets >100,000/µL; hemoglobin >9 g/dL (may be transfused to this level); ANC >1500 cells/µL.

• Adequate hepatic function as defined by the following: bilirubin <1.5 mg/dL; aspartate aminotransaminase (AST/SGOT) & alanine aminotransferase (ALT/SGPT) <2.5 x ULN or <5 x ULN if due to metastatic disease.

• Adequate renal function as defined by serum creatinine level <1.5 mg/dL.

Exclusion Criteria:

• Any active infection at study entry.

• Known diabetes or fasting blood glucose>160 mg/dL.

• Known human immunodeficiency virus (HIV).

• Any serious concomitant systemic disorders that in the opinion of the investigator would place the patient at excessive or unacceptable risk of toxicity.

• Surgery within the four weeks prior to the first dose

• Significant central nervous system (CNS) or psychiatric disorder(s) that preclude the ability of the patient to provide informed consent.

• Known or suspected brain metastases that have not received adequate therapy or for which the patient requires treatment with steroids or anticonvulsants. In the case of previously treated brain metastases, a minimum four week interval between completion of radiation therapy and registration on study with radiologic evidence of stable or responding brain metastases is required. In the setting of previous CNS metastasectomy, adequate (minimum four week) recovery from surgery and/or radiation therapy should be documented.

• Leptomeningeal brain metastases should be excluded regardless of whether the metastases have been treated or not.

• History of seizures, non-healing wounds, or arterial thrombosis.

• Unstable atrial or ventricular arrhythmias requiring control by medication; any cardiac ischemic event experienced within the preceding six months; prior history of congestive heart failure requiring therapy.

• Breastfeeding or pregnant (confirmed by serum ß-HCG within 10 days prior to the start of study treatment if applicable).

• Total gastrectomy, partial bowel obstruction or any gastrointestinal condition that may interfere with absorption of the study medication.

• Any condition that could jeopardize the safety of the patient and compliance with the protocol.

Related Conditions & MeSH terms

• Advanced Solid Tumors

Intervention

Drug:
• PX-866
Oral solution, dose escalation, once per day on days 1 to 5 and 8 to 12 or days 1-28 of a 28 day cycle, until progression or development of unacceptable toxicity

Locations

Country	Name	City	State
United States	University of Colorado Health Sciences Center	Aurora	Colorado
United States	M.D. Anderson Cancer Center	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Cascadian Therapeutics Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determine the MTD of PX-866		28 days
Primary	Evaluate the safety profile of PX-866		28 days
Primary	Evaluate pharmacodynamic measures of the effects of PX-866 on the phosphatidylinositol-3 kinase (PI-3K) pathway and related tumor markers.		28 days
Primary	Determine the PK profile of PX-866.		28 days
Secondary	Evaluate the anti-tumor activity of PX-866 in patients with advanced malignancies.		56 days