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Study to Determine the Relative Bioavailability, Single and Repeat Dose Pharmacokinetics, Safety and Tolerability of BOS172767 Enantiomers in Healthy Subjects

17 listopada 2020 zaktualizowane przez: Boston Pharmaceuticals

A Phase 1 Study to Determine the Relative Bioavailability of BOS172767 Enantiomer E1 and E2 and the Single and Repeat Dose Pharmacokinetics, Safety and Tolerability of BOS172767 Selected Enantiomer in Healthy Subjects

Part 1 of the study evaluates the safety and tolerability as well as pharmacokinetic properties of a single oral dose of BOS172767 enantiomer E1 and BOS172767 enantiomer E2 following administration to healthy participants. Part 2 of the study was to be conducted to assess the safety and tolerability as well as pharmacokinetic properties of one selected enantiomer (BOS172767-Ex) following multiple ascending doses over 14 days of dosing in healthy participants.

Przegląd badań

Status

Zakończony

Szczegółowy opis

The study design of Part 1 was a double-blind, placebo-controlled, randomized, single-dose, two-way crossover, followed by two sequential ascending dose periods in 12 healthy participants.

Part 2 was designed to be a double-blind, placebo-controlled, randomized multiple ascending dose (MAD) study in 36 healthy participants (12 per study cohort).

Part 2 was to progress following completion of Part 1, but was not conducted.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

12

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat do 50 lat (Dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Healthy males or healthy females of non-childbearing potential
  • Age 18 to 50 years at the time of signing informed consent
  • Body mass index (BMI) of 18.0 to 32.0 kilograms per meters squared (kg/m^2) as measured at screening
  • Must have been willing and able to communicate and participate in the whole study
  • Must have provided written informed consent
  • Must have agreed to adhere to the contraception requirements for this study

Exclusion Criteria:

  • Participants who received any investigational medicinal product (IMP) in a clinical research study within the 90 days prior to Day 1
  • Participants who were study site employees, or immediate family members of a study site or sponsor employee
  • Participants who had previously been enrolled and dosed in this study. Participants who had taken part in Part 1 were not permitted to take part in Part 2. Participants who had taken part in study QCL118174/BOS172767-01 (NCT03464058) were allowed to participate in this study.
  • History of any drug or alcohol abuse in the past 2 years
  • Regular alcohol consumption in males >21 units per week and females >14 units per week (1 unit = 1/2 pint beer, or a 25 milliliter [mL] shot of 40% spirit, 1.5 to 2 Units = 125 mL glass of wine, depending on type)
  • A confirmed positive alcohol breath test at screening or admission
  • Current smokers and those who had smoked within the last 6 months. A confirmed breath carbon monoxide reading of greater than 20 parts per million (ppm) at screening or admission.
  • Current users of e-cigarettes and nicotine replacement products and those who had used these products within the last 6 months
  • Females of childbearing potential including those who were pregnant or lactating (all female participants must have had a negative serum pregnancy test at screening and had a negative urine pregnancy test at all other time points). A woman was considered of childbearing potential unless she was permanently sterile (hysterectomy, bilateral salpingectomy, and bilateral oophorectomy) or was postmenopausal (had no menses for 12 months without an alternative medical cause and a serum follicle-stimulating hormone [FSH] concentration ≥40 International Units per Liter [IU/L])
  • Participants who did not have suitable veins for multiple venepunctures/cannulation as assessed by the investigator or delegate at screening
  • Clinically significant abnormal clinical chemistry, haematology, or urinalysis as judged by the investigator. Participants with Gilbert's Syndrome were not allowed.
  • Participants with alanine aminotransferase (ALT) > 1.5 x upper limit of normal (ULN) at screening (Part 1 and Part 2) or Day -1 (Part 2 only)
  • Confirmed positive drugs of abuse test result
  • Positive hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab), or human immunodeficiency virus (HIV) results
  • Evidence of renal impairment at screening, as indicated by an estimated creatinine clearance (CLcr) of <70 milliliters per minute (mL/min) using the Cockcroft-Gault equation
  • History of clinically significant cardiovascular, renal, hepatic, chronic respiratory, or gastrointestinal disease (including gall stones and/or cholecystectomy), or neurological or psychiatric disorder, as judged by the investigator
  • Serious adverse reaction or serious hypersensitivity to any drug or the IMP excipients
  • Presence or history of clinically significant allergy requiring treatment, as judged by the investigator. Hay fever was allowed unless it was active.
  • Donation or loss of greater than 400 mL of blood within the previous 3 months
  • Participants who were taking, or had taken, any prescribed or over-the-counter drug (other than 4 grams of paracetamol per day and/or hormone replacement therapy [HRT]) or herbal remedies in the 14 days before IMP administration. Exceptions may have applied on a case by case basis, if considered not to have interfered with the objectives of the study, as determined by the principal investigator.
  • Participants who had any ongoing fungal infections (stable toe nail onchomycosis was allowed)
  • Failure to satisfy the investigator of fitness to participate for any other reason

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Podstawowa nauka
  • Przydział: Randomizowane
  • Model interwencyjny: Zadanie sekwencyjne
  • Maskowanie: Potroić

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Part 1: Regimens AB(CD)
Participants received 50 milligrams (mg) BOS172767 E1 tablets or matching placebo (Regimen A) in the fasted state in Period 1, followed by 50 mg BOS172767 E2 tablets or matching placebo (Regimen B) in the fasted state in Period 2. In Period 3 and 4, participants received BOS172767-Ex (selected enantiomer from Part 1 [E1 or E2]) tablets or matching placebo (Regimens C and D, respectively) from Regimen A or B in the fasted state. The Period 3 and 4 dose was selected after review of data from Periods 1 and 2. In each Period, dosing occurred on Day 1, and there was a washout period of at least 10 days or 5 half-lives of the parent (whichever is greater) between each dose of investigational medicinal product.
Tabletki doustne
Oral tablets
Eksperymentalny: Part 1: Regimens BA(CD)
Participants received 50 milligrams (mg) BOS172767 E2 tablets or matching placebo (Regimen B) in the fasted state in Period 1, followed by 50 mg BOS172767 E1 tablets or matching placebo (Regimen A) in the fasted state in Period 2. In Period 3 and 4, participants received BOS172767-Ex (selected enantiomer from Part 1 [E1 or E2]) tablets or matching placebo (Regimens C and D, respectively) from Regimen A or B in the fasted state. The Period 3 and 4 dose was selected after review of data from Periods 1 and 2. In each Period, dosing occurred on Day 1, and there was a washout period of at least 10 days or 5 half-lives of the parent (whichever is greater) between each dose of investigational medicinal product.
Tabletki doustne
Oral tablets

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Part 1: Relative bioavailability of E1 versus E2 (Frel; exposure) of a single oral dose of BOS172767 enantiomer 1 (E1) and enantiomer 2 (E2) following administration to healthy participants based on Cmax, AUC(0-last), and AUC (0-inf)
Ramy czasowe: 24 hours post-dose for each of the four 6-day Periods
Cmax is defined as the maximum observed concentration. AUC(0-last) is defined as the area under the curve from 0 time to the last measurable concentration. AUC (0-inf) is defined as the area under the curve from 0 time extrapolated to infinity.
24 hours post-dose for each of the four 6-day Periods
Part 1: Number of participants with any treatment-emergent adverse event
Ramy czasowe: up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
Part 1: Number of participants with abnormal, clinically significant physical examination findings
Ramy czasowe: up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
Part 1: Number of participants with abnormal, clinically significant safety laboratory test findings
Ramy czasowe: up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
Part 1: Number of participants with abnormal, clinically significant vital sign values
Ramy czasowe: up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
Part 1: Number of participants with abnormal, clinically significant electrocardiogram findings
Ramy czasowe: up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
up to Day 6 of each Period; up to a 10-day Follow-up Period after last dose (up to Study Day 59)
Part 1: Plasma concentration of BOS172767 enantiomers 1 and 2
Ramy czasowe: 24 hours post-dose for each of the four 6-day Periods
24 hours post-dose for each of the four 6-day Periods
Part 1: Slope estimates (β) from the power model analysis on Cmax, AUC(0-last), and AUC(0-inf), as a measure of dose proportionality
Ramy czasowe: 24 hours post-dose for each of the four 6-day Periods
24 hours post-dose for each of the four 6-day Periods
Part 2: Plasma concentration of BOS172767-Ex (enantiomer E1 or E2)
Ramy czasowe: 24 hours post-dose
24 hours post-dose
Part 2: Number of participants with any treatment-emergent adverse event
Ramy czasowe: up to Day 24 of Part 2 (up to approximately 18 study weeks)
up to Day 24 of Part 2 (up to approximately 18 study weeks)
Part 2: Number of participants with abnormal, clinically significant physical examination findings
Ramy czasowe: up to Day 24 of Part 2 (up to approximately 18 study weeks)
up to Day 24 of Part 2 (up to approximately 18 study weeks)
Part 2: Number of participants with abnormal, clinically significant safety laboratory test findings
Ramy czasowe: up to Day 24 of Part 2 (up to approximately 18 study weeks)
up to Day 24 of Part 2 (up to approximately 18 study weeks)
Part 2: Number of participants with abnormal, clinically significant vital sign values
Ramy czasowe: up to Day 24 of Part 2 (up to approximately 18 study weeks)
up to Day 24 of Part 2 (up to approximately 18 study weeks)
Part 2: Number of participants with abnormal, clinically significant electrocardiogram findings
Ramy czasowe: up to Day 24 of Part 2 (up to approximately 18 study weeks)
up to Day 24 of Part 2 (up to approximately 18 study weeks)
Part 2: Slope estimates (β) from the power model analysis on Cmax, AUC(0-last), and AUC(0-inf), as a measure of dose proportionality
Ramy czasowe: 24 hours post-dose
24 hours post-dose

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

12 września 2019

Zakończenie podstawowe (Rzeczywisty)

22 stycznia 2020

Ukończenie studiów (Rzeczywisty)

22 stycznia 2020

Daty rejestracji na studia

Pierwszy przesłany

12 sierpnia 2020

Pierwszy przesłany, który spełnia kryteria kontroli jakości

12 sierpnia 2020

Pierwszy wysłany (Rzeczywisty)

14 sierpnia 2020

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

18 listopada 2020

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

17 listopada 2020

Ostatnia weryfikacja

1 listopada 2020

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • BOS172767-02
  • 2019-002289-11 (Numer EudraCT)
  • QSC201870 (Inny identyfikator: Quotient Sciences)

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

produkt wyprodukowany i wyeksportowany z USA

Tak

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Placebo

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