A Study to Investigate the Effect of Single and Repeated Oral Doses of ACT-539313 on What the Body Does to Flurbiprofen, Omeprazole, Midazolam in Healthy Subjects

NCT05254548 | Completed Phase 1

• 2 other identifiers: ID-082-1032021-006214-36
• Study Type: interventional
• Target: 22
• Locations: 1 country
• Sites: 1

Brief Summary

A study to investigate the effect of single and repeated oral doses of ACT-539313 on what the body does to flurbiprofen, omeprazole, midazolam in healthy participants.

Conditions

Healthy

Outcome Measures

Primary Outcomes (5)

• Maximum plasma concentration (Cmax) of each probe substrate: flurbiprofen, midazolam and omeprazole.

  In periods 1, 2 and 4 the plasma pharmacokinetic parameters of flurbiprofen, omeprazole, and midazolam will be derived by non-compartmental analysis of the plasma concentration-time profiles. Plasma pharmacokinetic samples will be collected at multiple predefined time points to analyze probe substrate: flurbiprofen, midazolam and omeprazole concentrations.

  Pre-dose through to 24 hours post-dose.

• Time to reach Cmax (tmax) of each probe substrate: flurbiprofen, midazolam and omeprazole.

  In periods 1, 2 and 4 the plasma pharmacokinetic parameters of flurbiprofen, omeprazole, and midazolam will be derived by non-compartmental analysis of the plasma concentration-time profiles. Plasma pharmacokinetic samples will be collected at multiple predefined time points to analyze probe substrate: flurbiprofen, midazolam and omeprazole concentrations.

  Pre-dose through to 24 hours post-dose.

• The area under the plasma concentration-time curve from zero to 24 hours (AUC0-24) of flurbiprofen, midazolam and omeprazole.

  In periods 1, 2 and 4 the plasma pharmacokinetic parameters of flurbiprofen, omeprazole, and midazolam will be derived by non-compartmental analysis of the plasma concentration-time profiles. Plasma pharmacokinetic samples will be collected at multiple predefined time points to analyze probe substrate: flurbiprofen, midazolam and omeprazole concentrations.

  Pre-dose through to 24 hours post-dose.

• The terminal elimination half-life (t½) of each probe substrate: flurbiprofen, midazolam and omeprazole.

  In periods 1, 2 and 4 the plasma pharmacokinetic parameters of flurbiprofen, omeprazole, and midazolam will be derived by non-compartmental analysis of the plasma concentration-time profiles. Plasma pharmacokinetic samples will be collected at multiple predefined time points to analyze probe substrate: flurbiprofen, midazolam and omeprazole concentrations.

  Pre-dose through to 24 hours post-dose.

• ACT-539313 trough plasma concentrations (Ctrough)

  In periods 2, 3 and 4 the plasma pharmacokinetic parameters of ACT-539313 will be measured prior to the next dose being administered in the morning.

  Pre-dose through to 10 days after first dose.

Other Outcomes (4)

• Treatment-emergent adverse events

  From study treatment administration on Day 1 up to last assessment at End of Study (Day 17).

• Maximum plasma concentration (Cmax) of ACT-539313

  Pre-dose through to 24 hours post-dose.

• Time to reach Cmax (tmax) of ACT-539313

  Pre-dose through to 24 hours after first dose.

Study Arms (1)

ACT-539313 with or without a standard combination (probe substrate)

EXPERIMENTAL

Treatment arm has 4 in-house treatment periods. In Treatment Period 1, participants will receive a single oral dose of the standardized combination (probe substrate: containing flurbiprofen \[50 mg\], midazolam \[2 mg\] and omeprazole 20 \[mg\]) on Day 1. Participants will be discharged from the study site on Day 2 and will be re-admitted on Day 7. In Treatment Period 2 (morning of Day 8) a first oral dose of 100 mg ACT-539313 will be administered. One hour later a single oral dose of the probe substrate will be administered. In the evening of Day 8, a second oral dose of 100 mg ACT-539313 will be administered. During Treatment Period 3 (morning of Day 9, ending on the evening of Day 14) oral doses of 100 mg ACT-539313 will be administered in the morning and evening. In Treatment Period 4 (Day 15), a single oral dose of 100 mg ACT-539313 together with the probe substrate will be administered. The participants will receive the last dose of ACT-539313 in the evening of Day 15.

Drug: ACT-539313; Drug: Flurbiprofen; Drug: Omeprazole; Drug: Midazolam

Interventions

ACT-539313 DRUG

100 mg ACT-539313 (hard capsules) will be administered twice per day in period 2 (morning and evening of Day 8), period 3 (morning and evening of Day 9 to 14) and period 4 (morning and evening of Day 15).

ACT-539313 with or without a standard combination (probe substrate)

Flurbiprofen DRUG

One daily dose of flurbiprofen 50 mg will be administered in period 1 (morning of Day 1), period 2 (morning of Day 8), and period 4 (morning of Day 15).

ACT-539313 with or without a standard combination (probe substrate)

Omeprazole DRUG

A single dose of omeprazole 20 mg will be administered in period 1 (morning of Day 1), period 2 (morning of Day 8), and period 4 (morning of Day 15).

ACT-539313 with or without a standard combination (probe substrate)

Midazolam DRUG

A single dose of midazolam 2 mg will be administered in period 1 (morning of Day 1), period 2 (morning of Day 8), and period 4 (morning of Day 15).

ACT-539313 with or without a standard combination (probe substrate)

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Signed informed consent in a language understandable to the participant prior to any study-mandated procedure.
• Healthy male or female subjects aged between 18 and 45 years (inclusive) at Screening.
• Body Mass Index of 18.5 to 28.0 kg/m2 (inclusive) at Screening.
• Women of childbearing potential must have a negative serum pregnancy test at Screening and a negative urine pregnancy test on Day -1. They must consistently and correctly use (from Screening, during the entire study, and for at least 30 days after study treatment intake) a highly effective method of contraception with a failure rate of \< 1% per year, be sexually inactive, or have a vasectomized partner. If a hormonal contraceptive is used, it must have been initiated at least 1 month before treatment administration.
• Women of non-childbearing potential, i.e., postmenopausal (defined as 12 consecutive months with no menses without an alternative medical cause, confirmed by a FSH test), with previous bilateral salpingectomy, bilateral salpingo-oophorectomy or hysterectomy, or with premature ovarian failure (confirmed by a specialist), XY genotype, Turner syndrome, uterine agenesis.
• lead ECG (including QT: \< 450 milliseconds \[for males\] and \< 470 milliseconds \[for females\] without clinically relevant abnormalities, measured after 5 min in the supine position at Screening and on Day -1.

You may not qualify if:

• Pregnant or lactating women.
• Any circumstances or conditions, which, in the opinion of the investigator, may affect full participation in the study or compliance with the protocol.
• Clinically relevant findings in clinical laboratory tests (hematology, clinical chemistry, and urinalysis, i.e. outside the reference ranges (\< 0.9 lower limit of normal and \> 1.1 upper limit of normal; except for relevant hepatic parameters \[Alanine Aminotransferase (ALT), Aspartate Aminotransferase Test (AST), bilirubin\] which must not exceed the upper limit of normal), at Screening and on Day -1.
• History of major medical or surgical disorders which, in the opinion of the investigator, are likely to interfere with the absorption, distribution, metabolism, or excretion of the study treatment(s) (appendectomy and herniotomy allowed, cholecystectomy not allowed).
• Acute, ongoing, recurrent, or chronic systemic disease with the ability to interfere with the evaluation of the study results.
• Prior history of severe respiratory failure, acute respiratory depression, or sleep apnea.
• Prior history of peptic ulcer disease and/or gastrointestinal bleeding.
• Prior history of asthma, urticaria, or other allergic type reactions after taking acetylsalicylic acid or other NSAIDs.
• History of cardiovascular thrombotic events (including myocardial infarction and stroke) and coronary artery bypass graft surgery.
• Participation in a clinical study involving study treatment administered within 3 months (or 5 t 1/2 of the study treatment administered \[whichever is longer\]) prior to screening or in more than 4 clinical studies within 1 year prior to Screening.
• Previous treatment with any prescribed medications (including vaccines) or over-the-counter (OTC) medications (including herbal medicines such as St. John's Wort, homeopathic preparations, vitamins, and minerals; with the exception of ibuprofen \[1200 mg/day\] or paracetamol \[up to 1500 mg/day\] up until Day -1) within 3 weeks (or 5 t1/2 \[whichever is longer\]) prior to first study treatment administration.

Sponsors & Collaborators

• Idorsia Pharmaceuticals Ltd.: lead

Study Sites (1)

CRS Clinical Research Services Berlin GmbH

Berlin, 13353, Germany

Location

Related Publications (1)

• Berger B, Kaufmann P, Berse M, Treiber A, Grignaschi N, Dingemanse J. Effect of nivasorexant (ACT-539313), a selective orexin-1-receptor antagonist, on multiple cytochrome P450 probe substrates in vitro and in vivo using a cocktail approach in healthy subjects. Pharmacol Res Perspect. 2023 Oct;11(5):e01143. doi: 10.1002/prp2.1143.

  PMID: 37800597 DERIVED

MeSH Terms

Interventions

ACT-539313; Flurbiprofen; Omeprazole; Midazolam

Intervention Hierarchy (Ancestors)

Propionates; Acids, Acyclic; Carboxylic Acids; Organic Chemicals; Biphenyl Compounds; Benzene Derivatives; Hydrocarbons, Aromatic; Hydrocarbons, Cyclic; Hydrocarbons; 2-Pyridinylmethylsulfinylbenzimidazoles; Sulfoxides; Sulfur Compounds; Pyridines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Benzimidazoles; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Benzodiazepines; Benzazepines

Study Officials

• Clinical Trials

  Idorsia Pharmaceuticals Ltd.

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: OTHER
• Intervention Model: SEQUENTIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Four-period, fixed-sequence drug-drug interaction study.

Study Record Dates

• First Submitted: February 15, 2022
• First Posted: February 24, 2022
• Study Start: February 18, 2022
• Primary Completion: April 13, 2022
• Study Completion: April 13, 2022
• Last Updated: May 4, 2022

Record last verified: 2022-05

Data Sharing

• IPD Sharing: Will not share

Locations

DE (1)