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Clinical Trials/NCT01692184
NCT01692184
Completed
Phase 1

A Phase 1, Two-part Study to Investigate the Safety and Pharmacokinetics of AVL-292 Following Multiple Oral Doses and to Evaluate the Effect of Food on the Pharmacokinetics of AVL-292 Following a Single Oral Dose in Healthy Adult Subjects

Celgene1 site in 1 country54 target enrollmentAugust 1, 2012

Overview

Phase
Phase 1
Intervention
50 mg AVL-292
Conditions
Healthy
Sponsor
Celgene
Enrollment
54
Locations
1
Primary Endpoint
Adverse Events
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This is a 2-part study. The first part is to evaluate the safety, pharmacokinetics (PK) and pharmacodynamics of AVL-292 following multiple oral doses; and the second part is to evaluate the effect of food on the pharmacokinetics of a single oral dose of AVL-292.

Detailed Description

Part 2 is an open-label, randomized, 2-period, 2-way crossover study to evaluate the effect of a standard high-fat breakfast on the pharmacokinetics of AVL-292. Ten subjects will be enrolled to receive 2 single doses of 200 mg AVL-292, one with food (i.e., fed) and the other without (i.e., fasted), in a randomized sequence.

Registry
clinicaltrials.gov
Start Date
August 1, 2012
End Date
October 8, 2012
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Celgene
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy male or female subjects of any ethnic origin between ages of 18 and 65 with a body mass index between 18 and 33

Exclusion Criteria

  • Recent history (i.e., within 3 years) of any clinically significant neurological, gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, endocrine, hematological, dermatological, psychological, ophthalmological, allergic or other major disorders;
  • Use of any prescribed systemic or topical medication within 30 days of the first dose;
  • Use of any non-prescribed systemic or topical medication (including vitamin/mineral supplements and herbal medicines, e.g., St. John's Wort) within 7 days of the first dose administration;
  • Exposure to an investigational drug (new chemical entity) within 30 days prior to the first dose administration

Arms & Interventions

50 mg of AVL-292 and Placebo

50 mg AVL-292 (2 x 25 mg AVL-292 capsules and 6 placebo capsules) once daily for 7 days administered orally under fasted condition

Intervention: 50 mg AVL-292

Placebo - 8 capsules

8 placebo capsules once daily for 7 days administered orally under fasted condition

Intervention: Placebo capsules

50 mg of AVL-292 and Placebo

50 mg AVL-292 (2 x 25 mg AVL-292 capsules and 6 placebo capsules) once daily for 7 days administered orally under fasted condition

Intervention: Placebo capsules

100 mg of AVL-292 and Placebo

100 mg AVL-292 (4 x 25 mg AVL-292 capsules and 4 placebo capsules) once daily for 7 days administered orally under fasted condition

Intervention: 100 mg AVL-292

100 mg of AVL-292 and Placebo

100 mg AVL-292 (4 x 25 mg AVL-292 capsules and 4 placebo capsules) once daily for 7 days administered orally under fasted condition

Intervention: Placebo capsules

200 mg AVL-292

8 x 25 mg AVL-292 capsules orally once daily for 7 days under fasted condition

Intervention: 200 mg AVL-292

350 mg of AVL-292

350 mg AVL-292 (14 x 25 mg AVL-292 capsules) once daily for 7 days administered orally under fasted condition

Intervention: 350 mg AVL-292

Placebo - 14 capsules

14 placebo capsules once daily for 7 days administered orally under fasted condition

Intervention: Placebo capsules

Outcomes

Primary Outcomes

Adverse Events

Time Frame: Up to 28 days after last AVL-292 dose

Number of participants with adverse events

PK-(Cmax)

Time Frame: 24 hours after the last AVL-292 dose on days 1 and 7

Maximum observed concentration in plasma

PK-(AUC)

Time Frame: 24 hours after the last AVL-292 dose days 1 and 7

Area under the plasma concentration-time curve

Secondary Outcomes

  • Pharmacodynamic response measured in percentage of target occupancy by AVL-292 in peripheral blood mononuclear cells(24 hours after the last AVL-292 dose days 1 and 7)

Study Sites (1)

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