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A Phase I Study to Determine the Effect of Food on the Pharmacokinetic Profile of BPI-7711

Phase 1
Completed
Conditions
NSCLC
Interventions
Registration Number
NCT04135820
Lead Sponsor
Beta Pharma, Inc.
Brief Summary

This is an open-label, randomised, single-dose, cross-over phase I study to evaluate the effect of food on the pharmacokinetic profile of BPI-7711 in Chinese healthy male subjects.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
16
Inclusion Criteria
  • Male, aged from 18 to 55 years.
  • BMI from 18.5 to 28.0 kg/m2
  • Medical history, vital signs, physical examination and lab tests are normal or abnormal without clinical significance.
Exclusion Criteria
  • Subjects with clinical significant diseases
  • Subjects with allergic disease history
  • Subjects with gastrointestinal disease history that can affect study drug absorption
  • Subjects with drug abuse history

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
High-fat mealBPI-7711BPI-7711 following a high-fat meal.
FastedBPI-7711BPI-7711 following a period of fasting
Primary Outcome Measures
NameTimeMethod
CmaxBlood samples collected on Day 1 and Day 15 at pre-dose, 1, 2, 4, 5, 6, 8, 10, 12, 24, 48, 72, 96, 120, 144 and 168 hours post BPI-7711 dose

Pharmacokinetics of BPI-7711 by assessment of maximum plasma concentration

AUC(0-last)Blood samples collected on Day 1 and Day 15 at pre-dose, 1, 2, 4, 5, 6, 8, 10, 12, 24, 48, 72, 96, 120, 144 and 168 hours post BPI-7711 dose

Pharmacokinetics of BPI-7711 by assessment of area under the plasma concentration time curve from zero to last assessed timepoint

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Shanghai Ninth People's Hospital

🇨🇳

Shanghai, China

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