A Study to Look at How a Single Oral Dose of 14C-OSI-906 is Absorbed, Broken Down and Eliminated in the Body

Advanced Solid Tumors Clinical Trial

Official title:

A Phase 1, Open-label Study to Investigate the Absorption, Metabolism, and Excretion of 14C-OSI-906 in Subjects With Advanced Solid Tumors With an Optional Treatment Phase

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01529684
• Other study ID #: OSI-906-104
• Status: Completed
• Phase: Phase 1
• Start date: March 19, 2012
• Est. completion date: February 20, 2013

Study information

• Verified date: February 2019
• Source: Astellas Pharma Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the pharmacokinetics, in particular the routes of excretion and extent of metabolism of OSI-906 after a single oral dose of 14C-labeled OSI-906. Subjects with Advanced Solid Tumors may participate and then continue into the Optional Treatment Phase.

Description:

This study includes two parts: Part A

Subjects will be admitted to the clinical research unit on Day -1 and remain confined to the unit until post dosing discharge criteria are met up to a maximum of 10 days. On Day 1, subjects will receive a single oral dose of 14C-labeled OSI-906.

Part B (optional)

Once the subject has completed part A, the subject may elect to continue participation in Part B. Subjects will receive OSI-906 (non-radiolabeled) twice daily by mouth. Subjects will be seen for scheduled visits every 7 days for the first 36 days and then every 21 days.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: February 20, 2013
• Est. primary completion date: December 8, 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• The subject has histologically or cytologically confirmed diagnosis of advanced solid tumor (measurable or non-measurable disease) for which no conventional therapy is available

• The subject has an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) = 2

• The subject has a predicted life expectancy =12 weeks

• The subject has a fasting glucose =125 mg/dL (7 mmol/L) at Screening, Day -1 and pre-dose Day 1

• The subject has adequate organ function defined by the following laboratory parameters:

• absolute neutrophil count (ANC) =1.5 x 10 9/L

• platelet count =100 x 10 9/L

• total bilirubin =1.5 x upper limit of normal (ULN)

• aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 2.5 x ULN, or = 5 x ULN if subject has documented liver metastases

• serum creatinine =1.5 x ULN

• potassium, calcium, and magnesium within normal limits or determined by the investigator to be not clinically significant (NCS)

• The subject has a negative cotinine test

• If male, is surgically sterile, or is using a medically acceptable method to prevent pregnancy and agrees to continue using this method while participating in the study and for 90 days after the last dose of study medication

• If female, the subject is surgically sterile or status post hysterectomy, post-menopausal, or is using 2 forms of medically acceptable methods of birth control, one of which must be a barrier method to prevent pregnancy and agrees to continue using this method from screening until 90 days after the last dose of study medication

• If female, the subject must not be breastfeeding at Screening, during the study period and for 90 days after last dose of study drug administration

• If female, the subject must not donate ova starting at Screening, and throughout the study period and for 90 days after last dose of study drug administration

• Female subject of child bearing potential has a negative pregnancy test at Screening and Day -1

Exclusion Criteria:

• The subject has Type 1 or Type 2 diabetes mellitus currently requiring insulinotropic or insulin therapy

• The subject has a history of poorly controlled gastrointestinal disorder (s) that could affect the absorption or metabolism of study drug

• The subject has used IGF-1R inhibitor therapy in last 6 months

• The subject has hepatocellular carcinoma

• The subject has used a CYP1A2 inhibitor or inducer within 14 days prior to Day 1

• The subject has used drugs with a risk of causing QTc interval prolongation and Torsade de Pointes (TdP) within 14 days prior to Day 1

• The subject has a history (within last 6 months) of significant cardio-vascular disease

• The subject has a history (within the last 6 months) of significant arrhythmia disease, unless the disease is well-controlled with medication per the Principal Investigator's clinical judgment

• The subject has had major surgery = 3 weeks prior to Day 1

• The subject has had radiation = 3 weeks prior to Day 1

• The subject has had chemotherapy = 3 weeks prior to Day 1

• The subject has participated in a radiolabeled study in the last 12 months

• The subject has a history of cerebrovascular accident (CVA) within 6 months prior to Day 1 or that resulted in ongoing neurologic instability

• The subject has an active infection or serious underlying medical condition (including any type of active seizure disorder within 12 months prior to Day 1) that would impair the ability of the subject to receive study drug

• The subject has participated in any interventional clinical study within 21 days or has been treated with any investigational drugs within 30 days or 5 half lives whichever is longer, prior to the initiation of Screening

• The subject has a history of any psychiatric condition that might impair the subject's ability to understand or to comply with the requirements of the study or to provide informed consent

• The subject is pregnant or lactating

• The subject has symptomatic brain metastases that are not stable, require steroids, or that have required radiation and/or other related treatment, (i.e., anti-epileptic medication) within 28 days prior to Day 1

• The subject has a history of allergic reactions attributed to compounds of similar chemical or biologic composition to the study drug

Related Conditions & MeSH terms

• Advanced Solid Tumors
• Pharmacokinetics of 14C-OSI-906

Intervention

Drug:
• radio-labeled OSI-906
Part A: oral solution of 14C-OSI-906
• OSI-906
Part B: oral tablets OSI-906

Locations

Country	Name	City	State
United States	Comprehensive Clinical Development NW, Inc.	Tacoma	Washington
United States	Northwest Medical Specialties, PLLC	Tacoma	Washington

Sponsors (1)

Lead Sponsor	Collaborator
Astellas Pharma Global Development, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Radioactivity in whole blood and plasma	Outcome measure for Part A: Area under the time concentration curve extrapolated to infinity (AUCinf), AUC from time of dosing to last quantifiable time point (AUClast), Maximum Plasma Concentration (Cmax), Time to maximum concentration (Tmax), Terminal half-life (t 1/2), Apparent Body Clearance after dosing (CL/F), and Apparent volume of distribution (Vz/F)	Up to 10 days from time of receipt of 14C-labeled OSI-906
Primary	Radioactivity ratio in blood/plasma	Outcome Measure for Part A of OSI-906 distribution between cellular components and plasma	Up to 10 days from time of receipt of 14C-labeled OSI-906
Primary	Excretion ratio and cumulative excretion of radioactivity in urine and feces	Outcome measure for Part A	Up to 10 days from time of receipt of 14C-labeled OSI-906
Primary	Composite of Pharmacokinetics of OSI-906 in plasma: AUC inf, AUC last, C max, t max, t 1/2, CL/F, and Vz/F	Outcome measure for Part A	Up to 10 days from time of receipt of 14C-labeled OSI-906
Primary	Composite of Pharmacokinetics of OSI-906 in urine: Cumulative amount of drug excreted into urine, feces or bile up to collection time of last measurable concentration (Ae last), Renal Clearance (CL R), and percentage of dose excreted (Ae last%)	Outcome measure for Part A	Up to 10 days from time of receipt of 14C-labeled OSI-906
Secondary	Metabolic Profile: Profiling of possible metabolites in OSI-906 plasma, urine, and feces	Outcome measure for Part A	Up to 10 days from time of receipt of 14C-labeled OSI-906
Secondary	Safety as assessed by recording adverse events, laboratory assessments and vital signs, and electrocardiograms (ECGs)	Outcome measures for Part A and Part B	For Part A: Days 1-10 and/or 30 days post treatment visit. For Part B: Treatment Period 1 (TP1) through 30 day post treatment visit (up to two years)

External Links

•   Link to results on the Astellas Clinical Study Results website