Bioequivalence Study of Different Aprocitentan Tablet Formulations

NCT05196399 | Completed Phase 1

• 2 other identifiers: ID-080-1102021-005090-11
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

Brief Summary

The main purpose is to study the pharmacokinetics of aprocitentan (ACT-132577) using 2 different tablet formulations. The clinical pharmacology data will be used to determine bioequivalence of 2 different tablet formulations.

Conditions

Healthy Subjects

Outcome Measures

Primary Outcomes (3)

• Maximum plasma concentration (Cmax) of aprocitentan

  Multiple pharmacokinetic sampling at predefined times on Day 1 (pre-dose) up to Day 10.

• The area under the plasma concentration-time curve from zero to time t of the last measured concentration above the limit of quantification (AUC0-t) of aprocitentan

  Multiple pharmacokinetic sampling at predefined times on Day 1 (pre-dose) up to Day 10.

• Area under the plasma concentration-time curve from zero to infinity (AUC0-inf) of aprocitentan

  Multiple pharmacokinetic sampling at predefined times on Day 1 (pre-dose) up to Day 10.

Secondary Outcomes (1)

• Treatment-emergent adverse events

  From study treatment administration on Day 1 up to last assessment at End of Period (Day 10).

Study Arms (2)

Aprocitentan (reference product)

EXPERIMENTAL

25 mg film-coated tablet

Drug: Aprocitentan (Formulation A)

Aprocitentan (test product)

EXPERIMENTAL

25 mg film-coated tablet

Drug: Aprocitentan (Formulation B)

Interventions

Aprocitentan (Formulation A) DRUG

A single oral dose of 25 mg.

Also known as: ACT-132577

Aprocitentan (reference product)

Aprocitentan (Formulation B) DRUG

A single oral dose of 25 mg.

Also known as: ACT-132577

Aprocitentan (test product)

Eligibility Criteria

• Age: 18 Years - 55 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 participant aged between 18 and 55 years (inclusive) at Screening.
• Body Mass Index of 18.0 to 30.0 kg/m2 (inclusive) at Screening.
• Systolic blood pressure (SBP) 100-140 mmHg, Diastolic blood pressure (DBP) 60-90 mmHg, and pulse rate 60-100 bpm (inclusive), measured on the dominant arm, after 5 min in the supine position at Screening and on Day 1 pre-dose of the first period.
• Woman of Childbearing Potential who has a negative serum pregnancy test at Screening and a negative urine pregnancy test on Day -1 of the first period. She must agree to consistently and correctly use (from Screening, during the entire study, and for at least 30 days after the last study treatment administration) a highly effective method of contraception with a failure rate of less than 1% per year.
• Woman of non-childbearing potential, i.e., postmenopausal (defined as 12 consecutive months with no menses without an alternative medical cause; in addition, an FSH test must be performed at Screening to further support postmenopausal status), with previous bilateral salpingectomy, bilateral salpingo oophorectomy or hysterectomy, or with premature ovarian failure (confirmed by a specialist), XY genotype, uterine agenesis.

You may not qualify if:

• Pregnant or lactating woman.
• Previous administration of aprocitentan.
• Known hypersensitivity to endothelin receptor antagonists or to excipients used in any of the formulations.
• 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 treatments (appendectomy and herniotomy allowed, cholecystectomy not allowed).
• Acute, ongoing, recurrent, or chronic systemic disease able to interfere with the evaluation of the study results.
• Clinically relevant findings on the physical examination at Screening and on Day -1 of the first period.
• Clinically relevant findings in clinical laboratory tests (hematology and clinical chemistry) at Screening and on Day -1 of the first period.
• Previous treatment with any prescribed medications (including vaccines) or over-the-counter medications (including herbal medicines such as St John's Wort, homeopathic preparations, vitamins, and minerals) within 3 weeks or 5 terminal elimination half-lives (t½; whichever is longer) prior to first study treatment administration.
• Legal incapacity or limited legal capacity at Screening.
• Positive COVID-19 test, if performed (subject to current epidemiological regulations in the Czech Republic) during the screening period.

Sponsors & Collaborators

• Idorsia Pharmaceuticals Ltd.: lead

Study Sites (1)

CEPHA s.r.o.

Pilsen, 323 00, Czechia

Location

MeSH Terms

Interventions

aprocitentan

Study Officials

• Clinical Trials

  Idorsia Pharmaceuticals Ltd.

  STUDY DIRECTOR

Study Design

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

Study Record Dates

• First Submitted: January 5, 2022
• First Posted: January 19, 2022
• Study Start: February 2, 2022
• Primary Completion: March 27, 2022
• Study Completion: April 7, 2022
• Last Updated: November 23, 2022

Record last verified: 2022-11

Data Sharing

• IPD Sharing: Will not share

Locations

CZ (1)