Studying Different Formulations of SR13668 in Healthy Volunteers

Healthy, no Evidence of Disease Clinical Trial

Official title:

Single-Dose Phase 0 Exploratory Pharmacokinetic Clinical Trial Comparing Five Oral Formulations of SR13668, an Orally Active AKT Pathway Inhibitor

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00896207
• Other study ID #: NCI-2009-01106
• Secondary ID: NCI-2009-01106MA
• Status: Completed
• Phase: Phase 1
• First received: May 8, 2009
• Last updated: October 7, 2014
• Start date: June 2009
• Est. completion date: March 2010

Study information

• Verified date: October 2011
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This randomized early phase I trial is studying different formulations of SR13668 in healthy volunteers. Giving SR13668 may help doctors learn more about how SR13668 is used by the body. It is not yet known which formulation of SR13668 is most effectively used by the body.

Description:

PRIMARY OBJECTIVES:

I. Determine which oral formulation of Akt inhibitor SR13668 provides the best bioavailability in normal, healthy volunteers.

SECONDARY OBJECTIVES:

I. Determine the oral pharmacokinetics of a single, low dose of Akt inhibitor SR13668 in healthy volunteers.

II. Characterize the metabolism of Akt inhibitor SR13668 in healthy volunteers. III. Collect preliminary safety data for Akt inhibitor SR13668 in healthy volunteers.

OUTLINE:

STAGE 1 (for the first 6 participants enrolled in the study [closed to accrual as of August, 2009]): Participants are randomized to 1 of 2 arms.

ARM I: Participants complete an overnight fast of ≥ 10 hours, eat a high-fat (approximately 50% of total caloric content of the meal) and high-calorie (approximately 800-1,000 calories), and then receive a single dose of oral SR13668 in a PEG400/Labrasol® liquid formulation with 8 ounces of water. Participants may not eat for ≥ 4 hours after study drug administration.

ARM II: Participants complete an overnight fast of ≥ 10 hours and then receive a single dose of oral SR13668 in a PEG400/Labrasol® liquid formulation with 8 ounces of water. Participants may not eat for ≥ 4 hours after study drug administration.

STAGE 2 (for the next 12 participants enrolled in the study): The preferred dietary condition (Arm I) identified in stage 1 is used. Participants are randomized to 1 of 4 arms.

ARM III: Participants receive a single dose of oral Akt inhibitor SR13668 in a Solutol® self-emulsifying solid dispersion capsule formulation.

ARM IV: Participants receive a single dose of oral Akt inhibitor SR13668 in a Solutol®/vitamin E TGPS self-emulsifying solid dispersion capsule formulation.

ARM V: Participants receive a single dose of oral Akt inhibitor SR13668 in a vitamin E TGPS self-emulsifying solid dispersion capsule formulation.

ARM VI: Participants receive a single dose of oral Akt inhibitor SR13668 in a Myrj 53 self-emulsifying solid dispersion capsule formulation.

Blood and urine samples are collected at baseline and periodically during the 24 hours after study drug administration for pharmacokinetic analysis by high performance liquid chromatography assay.

After completion of study treatment, participants are followed by telephone at 7-10 days and at 30 days.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: March 2010
• Est. primary completion date: March 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 62 Years

Eligibility

Inclusion Criteria:

• Healthy volunteer

• ECOG performance status 0

• Leukocyte count = 3,000/mm^3

• ANC = 1,500/mm^3

• Platelet count = 100,000/mm^3

• Hemoglobin normal

• Alkaline phosphatase = 1.5 times upper limit of normal (ULN)

• ALT = 1.5 times ULN

• Direct bilirubin = 1.5 times ULN

• Sodium = 1.5 times ULN

• Potassium = 1.5 times ULN

• Creatinine = 1.5 times ULN OR calculated creatinine clearance = 30 mL/min

• Fasting blood glucose normal

• Not pregnant or nursing

• Negative pregnancy test

• Fertile participants must use effective barrier contraception

• Able and willing to fast overnight prior to study drug administration AND consume a high-fat meal on the day of study drug administration

• Willing to provide required blood and urine samples AND stay all day and overnight in the Clinical Research Unit

• Willing to abstain from alcoholic beverages and caffeine for = 24 hours prior to study drug administration and until all blood and urine samples have been collected

• No cancer within the past 3 years except for nonmelanoma skin cancer, localized prostate cancer, superficial bladder cancer, or carcinoma in situ of the cervix

• No concurrent uncontrolled illness including, but not limited to, any of the following:

• Ongoing or active infection

• Symptomatic congestive heart failure

• Unstable angina pectoris

• Cardiac arrhythmia

• Severe chronic obstructive pulmonary disease requiring supplemental oxygen

• Hypertension that is difficult to control

• Psychiatric illness or social situation that would limit compliance with study requirements

• No diabetes mellitus

• No other condition that may, in the investigator's opinion, interfere with ingestion or absorption of oral medications (e.g., inflammatory bowel disease)

• No history of allergic-type reactions, including asthma and urticaria, or other intolerance to chemical compounds similar to the active study agent, indole-3-carbinol, or cruciferous vegetables (e.g., cabbage, cauliflower, broccoli, kale, and Brussels sprouts)

• More than 6 months since prior investigational agents

• More than 3 months since prior oral contraceptives (including Plan B method of contraception)

• No concurrent hormonal contraception

• More than 14 days since prior and no concurrent anticoagulant or antiplatelet medications

• More than 7 days since prior and no concurrent daily medications or nutritional supplements

• No prior gastrectomy that may, in the investigator's opinion, interfere with ingestion or absorption of oral medications

• No other concurrent medications

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Healthy, no Evidence of Disease

Intervention

Drug:
• Akt inhibitor SR13668
Given orally as a single dose

Locations

Country	Name	City	State
United States	Mayo Clinic	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Food effect on the bioavailability of SR13668 after oral administration	The first stage will be used to compare fed vs. fasted diet effect on the pharmacokinetics parameters under formulation 1.	Up to 30 days after completion of study treatment	No
Primary	Formulation effect on the bioavailability of SR13668 after oral administration	The second stage will be used to determine the formulation effects on the pharmacokinetics parameters, all under either fed or fasted diet as determined by the first stage.	Up to 30 days after completion of study treatment	No
Secondary	Solubility and stability of Akt inhibitor SR13668 in oral formulations selected for exploratory pharmacokinetics studies		Up to 30 days after completion of study treatment	No
Secondary	Oral pharmacokinetics of a single low dose of Akt inhibitor SR13668		Up to 30 days after completion of study treatment	No
Secondary	Metabolism of Akt inhibitor SR13668		Up to 30 days after completion of study treatment	No
Secondary	Preliminary safety data for Akt inhibitor SR13668, graded according to NCI CTCAE version 3.0		Up to 30 days after completion of study treatment	Yes