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Recombinant Human Alkaline Phosphatase in Healthy Japanese Subjects

11 marzo 2022 aggiornato da: AM-Pharma

A Double Blind, Randomized, Single Center, Single and Multiple Dose, Pharmacokinetic, Safety and Tolerability Study of Recombinant Human Alkaline Phosphatase (recAP) Administered Intravenously in Healthy Japanese Subjects

Clinical Phase 1 study to investigate the pharmacokinetics and to assess the safety and tolerability of recAP after single and multiple intravenous doses in healthy Japanese subjects.

Panoramica dello studio

Descrizione dettagliata

This study is a randomized, double blind, parallel group, single-center trial, consisting of a single dose part and a multiple dose part in 32 healthy Japanese subjects. Since all these doses have been studied before and safety extensively evaluated in non-Japanese subjects and no ethnic sensitivity is expected, the groups can be dosed in parallel.

Part A will have 3 parallel groups of 8 male subjects with N=6 on active and N=2 on placebo per group. Following baseline assessments, a single dose of recAP will be administered by a one-hour infusion followed by samplings for pharmacokinetic evaluation and routine safety assessments.

Part B will have a single group of 8 male subjects with N=6 on active and N=2 on placebo. Following baseline assessments, recAP will be dosed on Days 1, 2 and 3 by one-hour infusions followed by samplings for pharmacokinetic evaluation and routine safety assessments.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

34

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

      • Tokyo, Giappone, 192-0071
        • P-one clinic, Keikokai medical corporation

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 20 anni a 55 anni (Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Maschio

Descrizione

Inclusion Criteria:

  1. Gender : male
  2. Age : 20-55 years, inclusive
  3. Body mass index (BMI) : 18.0-30.0 kg/m2, inclusive
  4. Subjects must be Japanese by birth, have resided outside Japan <10 years, have parents and maternal and paternal grandparents who are Japanese, and primarily consume a Japanese diet.
  5. Resting supine blood pressure at screening showing no clinically relevant deviations from normal as judged by the Principal Investigator.
  6. Computerized (12-lead) ECG recording without signs of clinically relevant pathology or showing no clinically relevant deviations.
  7. All values for hematology and for clinical chemistry tests of blood and urine within the normal range or showing no clinically relevant deviations as judged by the Investigator.
  8. Ability and willingness to abstain from alcohol and tobacco products from 48 h prior to entry in the clinical research center until discharge.
  9. Easily accessible veins for venipuncture and catheter placing.
  10. Willingness to sign the written informed consent form (ICF).
  11. Subjects must agree to use adequate contraception when sexually active. This applies for the time period between end of first administration and 14 days after the last administration of study drug.

Exclusion Criteria:

  1. Evidence of clinically relevant pathology.
  2. History of relevant drug and/or food allergies.
  3. Subject has a history of clinically significant abnormalities or of any illness that, in the opinion of the study investigator, might confound the results of the study or poses an additional risk to the subject by their participation in the study.
  4. Use of medication, except for acetaminophen (paracetamol), which is allowed up to 3 days before entry into the clinical research center (after that time the use of a limited amount of acetaminophen is permitted after consultation with the Principal Investigator).
  5. Subject is mentally or legally incapacitated, has significant emotional problems at the time of screening visit or expected during the conduct of the study or has a history of a clinically significant psychiatric disorder over the last year.
  6. Participation in a drug study within 60 days prior to drug administration.
  7. Donation of more than 500 mL of blood within 60 days prior to drug administration. Donation of more than 1.5 liters of blood (for men) in the 10 months preceding the start of this study
  8. Smoking more than 5 cigarettes, 1 cigar or 1 pipe daily.
  9. History of alcohol abuse or drug addiction (including soft drugs like cannabis products).
  10. Positive drug screen (opiates, methadone, cocaine, amphetamines, cannabinoids, barbiturates, benzodiazepines, tricyclic antidepressants) and/or alcohol breath test at Screening and/or Pre-Dose.
  11. Intake of more than 14 units of alcohol per week (one unit of alcohol equals approximately 250 mL of beer, 100 mL of wine/Japanese Sake or 35 mL of spirits).
  12. Positive screen on hepatitis B surface antigen (HBsAg), anti-hepatitis C virus (anti-HCV) or anti-human immunodeficiency virus (anti-HIV)-1 or anti-HIV-2 or HIV-1/2 antigen.
  13. Illness within 5 days prior to (the first) drug administration.

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: Randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Group 1: single 1-hour IV infusion of 0.8 mg/kg recAP or placebo
single 1-hour IV infusion of 0.8 mg/kg recAP or placebo
Intravenous infusion
Intravenous infusion
Comparatore attivo: Group 2: single 1-hour IV infusion of 1.6 mg/kg recAP or placebo
single 1-hour IV infusion of 1.6 mg/kg recAP or placebo
Intravenous infusion
Intravenous infusion
Comparatore attivo: Group 3: single 1-hour IV infusion of 3.2 mg/kg recAP or placebo
single 1-hour IV infusion of 3.2 mg/kg recAP or placebo
Intravenous infusion
Intravenous infusion
Comparatore attivo: Group 4: 1-hour infusions of 1.6 mg/kg recAP or placebo on Days 1, 2 and 3
1-hour infusions of 1.6 mg/kg recAP or placebo on Days 1, 2 and 3
Intravenous infusion
Intravenous infusion

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Maximum observed recAP plasma concentration (Cmax) after single dose
Lasso di tempo: Single dose 9 days treatment phase
Blood collection for cmax evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
Time to attain maximum recAP serum concentration (Tmax) after single dose
Lasso di tempo: Single dose 9 days treatment phase
Blood collection for Tmax evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
Area under the plasma concentration versus time curve (AUC) after single dose
Lasso di tempo: Single dose 9 days treatment phase
Blood collection for AUC evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
recAP elimination half-life ( t1/2) after single dose
Lasso di tempo: Single dose 9 days treatment phase
Blood collection for t1/2 evaluation daily from Day 1 to Day 9
Single dose 9 days treatment phase
Maximum observed recAP plasma concentration (Cmax) after multiple doses
Lasso di tempo: Multiple doses 13 days treatment phase
Blood collection for cmax evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase
Time to attain maximum recAP serum concentration (Tmax) after multiple doses
Lasso di tempo: Multiple doses 13 days treatment phase
Blood collection for Tmax evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase
Area under the plasma concentration versus time curve (AUC) after multiple doses
Lasso di tempo: Multiple doses 13 days treatment phase
Blood collection for AUC evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase
recAP elimination half-life ( t1/2) after multiple doses
Lasso di tempo: Multiple doses 13 days treatment phase
Blood collection for t1/2 evaluation daily from Day 1 to Day 13
Multiple doses 13 days treatment phase

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Adverse events (AEs) after single dose
Lasso di tempo: Single dose 9 days treatment phase
Any untoward medical occurrence in a subject enrolled into a clinical study regardless of its causal relationship to study drug.
Single dose 9 days treatment phase
Adverse events (AEs) after multiple doses
Lasso di tempo: Multiple doses 13 days treatment phase
Any untoward medical occurrence in a subject enrolled into a clinical study regardless of its causal relationship to study drug.
Multiple doses 13 days treatment phase

Collaboratori e investigatori

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

Sponsor

Investigatori

  • Direttore dello studio: Annelies Legters, AM-Pharma

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 (Effettivo)

7 maggio 2021

Completamento primario (Effettivo)

8 luglio 2021

Completamento dello studio (Effettivo)

31 dicembre 2021

Date di iscrizione allo studio

Primo inviato

25 maggio 2021

Primo inviato che soddisfa i criteri di controllo qualità

9 giugno 2021

Primo Inserito (Effettivo)

11 giugno 2021

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

14 marzo 2022

Ultimo aggiornamento inviato che soddisfa i criteri QC

11 marzo 2022

Ultimo verificato

1 marzo 2022

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • AP-recAP-AKI-01-02

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

No

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

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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