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Recombinant Human Alkaline Phosphatase in Healthy Japanese Subjects

11 mars 2022 uppdaterad av: 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.

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Faktisk)

34

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Tokyo, Japan, 192-0071
        • P-One Clinic, Keikokai Medical Corporation

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

20 år till 55 år (Vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Manlig

Beskrivning

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.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Sekventiell tilldelning
  • Maskning: Fyrdubbla

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: 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
Aktiv komparator: 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
Aktiv komparator: 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
Aktiv komparator: 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

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Maximum observed recAP plasma concentration (Cmax) after single dose
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Adverse events (AEs) after single dose
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Utredare

  • Studierektor: Annelies Legters, AM-Pharma

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

7 maj 2021

Primärt slutförande (Faktisk)

8 juli 2021

Avslutad studie (Faktisk)

31 december 2021

Studieregistreringsdatum

Först inskickad

25 maj 2021

Först inskickad som uppfyllde QC-kriterierna

9 juni 2021

Första postat (Faktisk)

11 juni 2021

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

14 mars 2022

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

11 mars 2022

Senast verifierad

1 mars 2022

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • AP-recAP-AKI-01-02

Plan för individuella deltagardata (IPD)

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Nej

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