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Safety and Pharmacokinetics of AT1001 (Migalastat HCl) in Healthy Subjects and Subjects With Impaired Renal Function

2 agosto 2017 aggiornato da: Amicus Therapeutics

An Open-Label Study to Determine the Safety and Pharmacokinetics of AT1001 in Subjects With Impaired Renal Function and Healthy Subjects With Normal Renal Function (AT1001-015)

This study will assess the safety, tolerability, and pharmacokinetics (PK) study of a single dose of 150 mg AT1001 (migalastat HCl, GR181413A) administered orally to healthy subjects with normal renal function and to subjects with mild, moderate, and severe renal impairment.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

This will be an open-label, non-randomized, multiple-center, sequential group, safety, tolerability, and PK study of a single dose of AT1001 (migalastat HCl, GR181413A) administered orally as a 150 mg dose in fasted healthy control male and female subjects with normal renal function compared to mild, moderate, and severe renally-impaired subjects (classified by level of creatinine clearance [CLcr] as determined by the Cockcroft-Gault formula).

Screening will occur from Day -28 to Day -2. Subjects will check-in to the clinic on Day -1 and receive a single oral dose of 150 mg AT1001 on Day 1. Subjects will be discharged from the clinic on Day 2 (if stable as determined by the Investigator) and return for daily visits on Day 3 through Day 6 for a safety assessment and PK sampling. Subjects will undergo a follow-up visit on Day 7 (+1) and an end of study visit on Day 10 (+1).

Tipo di studio

Interventistico

Iscrizione (Effettivo)

32

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • California
      • Costa Mesa, California, Stati Uniti, 92626
        • GSK Investigational Site
    • Florida
      • Miami, Florida, Stati Uniti, 33169
        • GSK Investigational Site
      • Miami, Florida, Stati Uniti, 33014
        • GSK Investigational Site
      • Orlando, Florida, Stati Uniti, 32809
        • GSK Investigational Site

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 75 anni (Adulto, Adulto più anziano)

Accetta volontari sani

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria All subjects

  • males or females aged 18 to 70 years inclusive (subjects with normal renal function, mild or moderate renal impairment), and 18 to 75 years inclusive (subjects with severe renal impairment)
  • body mass index 18.0 to 40.0 kilogram (kg)/square meter (m^2) inclusive
  • females who are non-pregnant, non-lactating, or postmenopausal for >=1 year, surgically sterile for >= 90 days, or agree to use approved methods of contraception
  • males will be sterile or use approved methods of contraception
  • understands and signs informed consent form Healthy subjects with normal renal function
  • negative test for selected drugs of abuse (excludes alcohol) at Screening and Check-in
  • good health with no clinically significant medical history, physical examination, vital signs, or 12-lead ECG
  • clinical laboratory tests within the reference range or not clinically significant
  • normal renal function (estimated CLcr >90 mL/min) at Screening Subjects with mild, moderate or severe renal impairment
  • negative test for selected drugs of abuse (excludes alcohol) at Screening and Check-in or verification of a prescription for a positive test
  • renal impairment (estimated CLcr <90 mL/min)
  • evidence of stable renal impairment defined as two separate estimated CLcr values within 25%
  • clinical laboratory results consistent with their renal condition or of no clinical significance for the study
  • abnormal laboratory values must not be clinically significant. Anemia secondary to renal disease is acceptable if hemoglobin is ≥9 g/dL and no clinically significant symptoms. Liver enzymes and bilirubin must be below twice the upper normal level
  • subjects with renal impairment must have stable underlying medical conditions < 90 days before study start
  • stable medication regimen(s) (no new drug(s) or changed dosage(s) <30 days before study drug)
  • in good general health, allowing for concurrent illnesses associated with chronic kidney disease

Exclusion Criteria:

All subjects:

  • history of hypersensitivity or allergies to any drug, unless approved by the Investigator and reviewed by Sponsor/Medical Monitor
  • participation in a study with receipt of an investigational drug < 5 half-lives or 30 days (whichever is longer) before Check-in
  • use of alcohol, grapefruit, or caffeine-containing foods or beverages < 72 hours before Check-in, unless approved by the Investigator and reviewed by the Sponsor/Medical Monitor
  • poor peripheral venous access
  • whole blood donation < 56 days before dosing or plasma donation < 14 days before dosing
  • receipt of blood products < 2 months before Check-in
  • history or presence of any clinically significant abnormal ECG
  • history of alcoholism or drug addiction < 1 year before Check-in
  • positive test for HIV antibody, HBsAg or anti-HCV
  • pregnant or breastfeeding

Healthy subjects with normal renal function:

  • use of any tobacco- or nicotine-containing products < 6 months before Check-in
  • clinically significant (history of or active) cardiac, hepatic, pulmonary, endocrine, neurological, infectious, gastrointestinal, hematologic, oncologic, or psychiatric disease putting the subject at increased risk or could interfere with study objectives
  • screening laboratory values outside normal range and deemed clinically significant by the Investigator
  • use of a prescription drug < 14 days of dosing or a non-prescription drug < 7 days before dosing or need of concomitant medication during the study

Subjects with mild, moderate, or severe renal impairment:

  • unstable disease (concurrent medical conditions that have changed significantly < 90 days)
  • changes in concomitant prescription medications < 30 days before dosing or expected changes during study
  • use of new non-prescription medication < 30 days before dosing
  • renal transplant
  • acute or chronic non-renal condition limiting the subject's ability to complete and/or participate in the study

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: AT1001 150 mg
Each subject will receive a single oral dose of AT1001 150 mg administered orally with 240 mL room temperature water after at least a 4-hour fast
AT1001 150mg is available as a capsule
Altri nomi:
  • migalastat HCl
  • GR181413A

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of subjects with adverse events to assess safety and tolerability
Lasso di tempo: Day 1 to Day 10 (+1)
Adverse events will be evaluated from Day 1 to the end of study (Day 10 +1).
Day 1 to Day 10 (+1)
Clinical laboratory test values to assess safety and tolerability
Lasso di tempo: Day -28 to Day 10 (+1)
Clinical laboratory evaluations (hematology, clinical chemistry, urinalysis, Hepatitis A and HIV screen) will be evaluated from screening to the end of the study.
Day -28 to Day 10 (+1)
Vital signs to assess safety and tolerability
Lasso di tempo: Day -28 to Day 10 (+1)
Vital signs (oral temperature, respiratory rate, and seated blood pressure) will be performed from screening to the end of the study.
Day -28 to Day 10 (+1)
Physician examination to assess safety and tolerability
Lasso di tempo: Day -28 to Day 10 (+1)
Physical examination (general appearance, skin, thorax/lungs, cardiovascular and abdomen) will be performed from screening to the end of the study.
Day -28 to Day 10 (+1)
Measure of ECG to assess safety and tolerability
Lasso di tempo: Day -28 to Day 10 (+1)
Electrocardiogram (ECG) measures the electrical activity of the heart and the hearts' rhythm. All subjects will undergo ECG testing.
Day -28 to Day 10 (+1)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Maximum observed concentration (Cmax) of AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and the resultant maximum plasma concentration (Cmax) will be measured in subjects with impaired renal function and normal renal function.
Day 1 to Day 6
Time to achieve maximum concentration (Tmax) of AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and time to maximum concentration (tmax) will be measured in subjects with impaired renal function and normal renal function.
Day 1 to Day 6
Apparent terminal elimination half life (t1/2 ) of AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and and apparent terminal elimination half-life (t1/2) will be measured in subjects with impaired renal function and normal renal function.
Day 1 to Day 6
Area under the concentration-time curve from time zero to the last measurable concentration (AUC 0-t ) of AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and AUC 0-t will be measured in subjects with impaired renal function and normal renal function
Day 1 to Day 6
Area under the concentration-time curve extrapolated to infinity (AUC 0-inf) of AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and AUC 0-inf will be measured in subjects with impaired renal function and normal renal function
Day 1 to Day 6
Apparent terminal elimination rate constant for AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and the apparent terminal elimination rate constant will be measured in subjects with impaired renal function and normal renal function
Day 1 to Day 6
Oral clearance of AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and the oral clearance will be measured in subjects with impaired renal function and normal renal function
Day 1 to Day 6
Oral volume of distribution of AT1001
Lasso di tempo: Day 1 to Day 6
Blood samples will be collected at predose, and 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 24, 48, 72, 96, and 120 hours post-dose and the oral volume of distribution will be measured in subjects with impaired renal function and normal renal function
Day 1 to Day 6

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 agosto 2011

Completamento primario (Effettivo)

1 aprile 2012

Completamento dello studio (Effettivo)

1 aprile 2012

Date di iscrizione allo studio

Primo inviato

8 novembre 2012

Primo inviato che soddisfa i criteri di controllo qualità

15 novembre 2012

Primo Inserito (Stima)

21 novembre 2012

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

3 agosto 2017

Ultimo aggiornamento inviato che soddisfa i criteri QC

2 agosto 2017

Ultimo verificato

1 agosto 2017

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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Prove cliniche su AT1001 150 mg

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