A Study to Compare the Relative Bioavailability of Two AG-881 Formulations and Evaluate the Effect of Food and Omeprazole on the Pharmacokinetics of AG-881

NCT ID: NCT04128787

Last Updated: 2021-07-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-09-30
• Study Completion Date: 2019-12-18

Brief Summary

The purpose of this study is to compare the single-dose pharmacokinetics (PK) of two formulations (Formulation 1 and Formulation 2) of AG-881 and to examine the effect of food and multiple-dose omeprazole on the single-dose PK of AG-881 Formulation 2 in healthy adult participants. This study will also assess the safety and tolerability of single-dose AG-881 (Formulation 1 and 2) alone and of AG-881 Formulation 2 when administered with and without food and when coadministered with omeprazole in healthy adult subjects.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment Sequence ABCD

Participants will receive Treatment A (AG-881 Formulation 1, 50 mg, tablet orally, under fasted condition once on Day 1 of Period 1) followed by Treatment B (AG-881 Formulation 2, 50 mg, tablet orally, under fasted condition once on Day 1 of Period 2) followed by Treatment C (AG-881 Formulation 2, 50 mg, tablet, orally, under fed condition once on Day 1 of Period 3) followed by Treatment D (omeprazole 40 mg capsule, orally, once daily on Days 1 to 4 and AG-881 Formulation 2, 50 mg, tablet, orally, under fasted condition, once on Day 4 of Period 4). Each period will be separated by a Washout Period of 21 days.

Group Type: EXPERIMENTAL

AG881 Formulation 1

Intervention Type: DRUG

AG881 uncoated tablets

AG881 Formulation 2

Intervention Type: DRUG

AG881 film-coated tablets

Omeprazole

Intervention Type: DRUG

Omeprazole capsules

Treatment Sequence BCAD

Participants will receive Treatment B in Period 1 followed by Treatment C in Period 2 then Treatment A in Period 3 followed by Treatment D in Period 4. Each period will be separated by a Washout Period of 21 days.

Group Type: EXPERIMENTAL

AG881 Formulation 1

Intervention Type: DRUG

AG881 uncoated tablets

AG881 Formulation 2

Intervention Type: DRUG

AG881 film-coated tablets

Omeprazole

Intervention Type: DRUG

Omeprazole capsules

Treatment Sequence CABD

Participants will receive Treatment C in Period 1 followed by Treatment A in Period 2 then Treatment B in Period 3 followed by Treatment D in Period 4. Each period will be separated by a Washout Period of 21 days.

Group Type: EXPERIMENTAL

AG881 Formulation 1

Intervention Type: DRUG

AG881 uncoated tablets

AG881 Formulation 2

Intervention Type: DRUG

AG881 film-coated tablets

Omeprazole

Intervention Type: DRUG

Omeprazole capsules

Interventions

AG881 Formulation 1

AG881 uncoated tablets

Intervention Type: DRUG

AG881 Formulation 2

AG881 film-coated tablets

Intervention Type: DRUG

Omeprazole

Omeprazole capsules

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy, adult, male or female (WONCBP) participants, 18-55 years of age, inclusive, at Screening.

2. Continuous non-smoker who has not used nicotine-containing products for at least 3 months prior to the first dosing and throughout the study.

3. Body mass index (BMI) ≥ 18.0 and ≤ 32.0 kg/m2 at Screening.

4. Medically healthy with no clinically significant medical history, physical examination, laboratory profiles, vital signs, or ECG, as deemed by the Investigator or designee. Liver function tests (serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and bilirubin [total and direct]) must be ≤ the upper limit of normal (ULN).

5. Female participants must be of non-childbearing potential defined as a female who has undergone one of the following sterilization procedures at least 6 months prior to the first dosing: hysteroscopic sterilization; bilateral tubal ligation or bilateral salpingectomy; hysterectomy; bilateral oophorectomy or is postmenopausal with amenorrhea for at least 1 year prior to the first dosing and follicle-stimulating hormone (FSH) serum levels consistent with postmenopausal status.

6. A non-vasectomized, male participants must agree to use a condom with spermicide or abstain from sexual intercourse during the study until 90 days after the last dosing. (No restrictions are required for a vasectomized male provided his vasectomy has been performed 4 months or more prior to the first dosing of study drug. A male who has been vasectomized less than 4 months prior to study first dosing must follow the same restrictions as a non-vasectomized male).

7. If a male participants, must agree not to donate sperm from the first dosing until 90 days after the last dosing.

8. Understands the study procedures in the informed consent form (ICF), and be willing and able to comply with the protocol.

Exclusion Criteria

1. Participant is mentally or legally incapacitated or has significant emotional problems at the time of the Screening visit or expected during the conduct of the study.

2. History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the Investigator or designee.

3. History of any illness that, in the opinion of the Investigator or designee, might confound the results of the study or pose an additional risk to the participant (e.g., history or presence of rashes) by their participation in the study.

4. History of stomach or intestinal surgery that would potentially alter absorption/secretion; or any major surgical procedure within the previous 3 months prior to Screening.

5. History of severe and/or uncontrolled ventricular arrhythmias, or other factors that increase the risk of QT prolongation or arrhythmic events (e.g., heart failure, hypokalemia, family history of long QT interval syndrome).

6. History or presence of alcoholism or drug abuse within the past 2 years prior to the first dosing.

7. History or presence of hypersensitivity or idiosyncratic reaction to the study drugs or related compounds.

8. Any positive responses on the C-SSRS.

9. Female participants of childbearing potential.

10. Female participants with a positive pregnancy test or who are lactating.

11. Positive urine drug or alcohol results at Screening or first check-in.

12. Positive results at Screening for human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV) antibodies.

13. QT interval Fridericia's formula (QTcF) interval is >450 msec, or QRS interval >110 msec, or PR interval >220 msec, or participants who have ECG findings deemed abnormal with clinical significance by the Investigator or designee at Screening.

14. Seated blood pressure is less than 90/40 mmHg or greater than 140/90 mmHg at Screening.

15. Seated heart rate is lower than 40 beats per minute (bpm) or higher than 99 bpm at Screening.

16. Estimated creatinine clearance <90 mL/min at Screening.

17. Unable to refrain from or anticipates the use of: Any drug, including prescription and non-prescription medications, herbal remedies, and vitamin supplements, beginning 14 days prior to the first dosing and throughout the study. After first dosing, ibuprofen (1.2 g per 24 hour) may be administered at the discretion of Investigator or designee. Hormone replacement therapy will not be allowed; any drugs known to be strong inducers of CYP3A, CYP2C9, or CYP2C19 enzymes including St. John's Wort and/or, gastric acid reducing agents (e.g., proton-pump inhibitors [with the exception of omeprazole administered as part of the study schedule], H2-receptor antagonists, antacids) for 28 days, or drugs that can prolong the QT interval for 21 days, prior to the first dosing and throughout the study. Appropriate sources (e.g., Flockhart TableTM) will be consulted to confirm lack of PK/Pharmacodynamic (PD) interaction with study drug.

18. Refuses to abstain from alcohol from 48 hours prior to the first dosing and throughout the study.

19. Refuses to abstain from grapefruit-containing foods or beverages or Seville orange containing foods or beverages from 14 days prior to the first dosing and throughout the study.

20. Has been on a diet incompatible with the on-study diet, in the opinion of the Investigator or designee, within the 30 days prior to the first dosing and throughout the study.

21. Any allergy or intolerance to food substances which will be provided on the study.

22. Is lactose intolerant.

23. Donation of blood or significant blood loss within 56 days prior to the first dose.

24. Plasma donation within 7 days prior to the first dose.

25. Receipt of blood or blood products within 2 months prior to the first dose.

26. Participation in another clinical study within 30 days prior to the first dose. The 30-day window will be derived from the date of the last blood collection or dosing, whichever is later, in the previous study to Day 1 of Period 1 of the current study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Agios Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Affairs

Role: STUDY_CHAIR

Agios Pharmaceuticals, Inc.

Locations

Celerion

Tempe, Arizona, United States

Countries

United States

Other Identifiers

AG881-C-007

Identifier Type: -

Identifier Source: org_study_id