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A Single and Multiple Doses Safety, Tolerability, Pharmacokinetics and Food Effect Study of KVD824 in Healthy Volunteers

2 février 2022 mis à jour par: KalVista Pharmaceuticals, Ltd.

A Randomized, Double-blind, Placebo-controlled, Single and Multiple Ascending Doses Study of the Safety, Tolerability, and Pharmacokinetics of KVD824 Followed by Crossover Food Effect Sub-study in Healthy Volunteers

This is a 3 part phase 1, randomized, double-blind, placebo-controlled, study of the safety, tolerability, and pharmacokinetics of KVD824 following administration of single and multiple ascending oral doses; followed by a crossover food effect sub-study in healthy male volunteers.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

Part A was a single-centre randomized, double blinded, placebo control to investigate the safety and tolerability of single ascending doses of KVD824 administered to healthy male volunteers.

Part B was a single centre, randomized, double blinded, placebo control to investigate the safety and tolerability of multiple ascending doses of KVD824 administered to healthy male volunteers.

Part C was a single-centre, open labelled to investigate the food effect.

Type d'étude

Interventionnel

Inscription (Réel)

108

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Merthyr Tydfil, Royaume-Uni
        • KalVista Investigative Site

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 55 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Homme

La description

Inclusion Criteria:

  • Healthy male subjects between 18 and 55 years of age.
  • Healthy subjects as determined by past medical history and as judged by the Chief Investigator / deputy.
  • Male subject willing to wear a condom and whose partner of child bearing potential uses a highly effective method of contraception (e.g. partner use of intrauterine device (IUD)) or an effective method of contraception, i.e., established method of contraception + condom, if applicable (unless anatomically sterile or where abstaining from sexual intercourse is in line with the preferred and usual lifestyle of the subject) from first dose until 3 months after last dose of IMP. Men whose partners are already pregnant must continue to use a condom during the trial and for three months thereafter.
  • Subject with a body mass index (BMI) of 18-32 kg/m2.
  • Subject with no clinically significant history of previous allergy / sensitivity to KVD824 or any of the excipients contained within the Investigational Medicinal Product.
  • Subject with no clinically significant abnormal serum biochemistry, haematology, clotting profiles, and urine examination values within 28 days before the first dose of Investigational Medicinal Product.
  • Subject with a negative urinary drugs of abuse screen, determined within 28 days before the first dose of Investigational Medicinal Product (N.B. a positive result may be repeated at the Chief Investigator's discretion).
  • Subject with negative human immunodeficiency virus (HIV) and hepatitis B surface antigen (Hep B) and hepatitis C virus antibody (Hep C) results.
  • Subject with no clinically significant abnormalities in 12-lead electrocardiogram (QTcF ≤ 430 ms and PR interval 120-220 ms) determined within 28 days before first dose of Investigational Medicinal Product.
  • Subject with no clinically significant abnormalities in vital signs (supine systolic (≤140 mmHg) and diastolic blood pressure (≤ 90 mmHg), pulse (≤ 100 bpm), oral temperature (≤ 37.5°C)) determined within 28 days before first dose of Investigational Medicinal Product.
  • Subjects must not donate sperm from first dose until at least 3 months after last dose of Investigational Medicinal Product.
  • Subjects without any special food restrictions that would hinder ability to consume gelatin (Part A and Part B placebo), or the high fat breakfast provided during study Part C; such as vegetarian, lactose intolerance, vegan, low-fat, low sodium, etc.
  • Subjects with no known allergy or sensitivity to lactose and/or any additional excipients contained in Investigational Medicinal Product.
  • Subject must be available to complete the study (including all follow up visits).
  • Subject must satisfy the Chief Investigator / deputy about their fitness to participate in the study.
  • Subject must provide written informed consent to participate in the study.

Exclusion Criteria:

  • A clinically significant history of gastrointestinal disorder likely to influence Investigational Medicinal Product absorption.
  • Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements within 28 days or 5 half-lives (which ever is longer) prior to the first dose of Investigational Medicinal Product, unless in the opinion of the Chief Investigator the medication will not interfere with the study procedures or compromise subject safety.
  • Evidence of renal, hepatic, central nervous system, respiratory, cardiovascular or metabolic dysfunction.
  • Subjects with a history of clotting abnormalities.
  • A clinically significant history of drug or alcohol abuse in the last 5 years.
  • Users of nicotine products i.e., current smokers or ex-smokers who have smoked within the 6 months prior to dosing with the study medication or users of cigarette replacements (e.g., e-cigarettes, nicotine patches or gums).
  • Inability to communicate well with Investigators (i.e., language problem, poor mental development or impaired cerebral function).
  • Participation in a New Chemical Entity clinical study within the previous 3 months or a marketed drug clinical study within the 30 days before the first dose of Investigational Medicinal Product. (Washout period between studies is defined as the period of time elapsed between the last dose of the previous study and the first dose of the next study).
  • Donation of 450 mL or more blood within the 3 months before the first dose of Investigational Medicinal Product.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation croisée
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Part A - KVD824 - 10 mg
6 participants were administered10 mg of KVD824 in capsule form (1 x 10 mg capsule) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part A - KVD824 - 20 mg
6 participants were administered 20mg of KVD824 in capsule form ( 2 x 10 mg capsules) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part A - KVD824 - 40 mg
6 participants were administered 40mg of KVD824 in capsule form (1 x 40 mg capsule) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part A - KVD824 - 80 mg
6 participants were administered 80mg of KVD824 in capsule form (2 x 40 mg capsules) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part A - KVD824 - 160mg
6 participants were administered 160mg of KVD824 in capsule form (1 x 160 mg capsule) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part A - KVD824 - 320 mg
6 participants were administered 320mg of KVD824 in capsule form (1 x 320 mg capsule) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part A - KVD824 - 640 mg
6 participants were administered 640 mg of KVD824 in capsule form (2 x 320 mg capsule) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part A - KVD824 - 1280 mg
6 participants were administered 1280 mg of KVD824 in capsule form (4 x 320 mg capsule) on one occasion on Day 1. 2 participants received matching placebo.
Active
Placebo
Expérimental: Part B - KVD824 - 80 mg Multi-Dose
6 participants were administered 80 mg of KVD824 in capsule form (2 x 40 mg capsules) in multiple doses over a period of 5 days (twice a day on Days 1-4 and once in morning of Day 5; the first dose on each day was administered fasted). 2 participants received matching placebo.
Active
Placebo
Expérimental: Part B - KVD824 - 160 mg Multi-Dose
6 participants were administered 160mg of KVD824 in capsule form (1 x 160 mg capsule) in multiple doses over a period of 5 days (twice a day on Days 1-4 and once in morning of Day 5; the first dose on each day was administered fasted). 2 participants received matching placebo.
Active
Placebo
Expérimental: Part B - KVD824 - 320 mg Multi-Dose
6 participants were administered 320mg of KVD824 in capsule form (1 x 320 mg capsule) in multiple doses over a period of 5 days (twice a day on Days 1-4 and once in morning of Day 5; the first dose on each day was administered fasted). 2 participants received matching placebo.
Active
Placebo
Expérimental: Part B - KVD824 - 640 mg Multi-Dose
6 participants were administered 640mg of KVD824 in capsule form (2 x 320 mg capsules) in multiple doses over a period of 5 days (twice a day on Days 1-4 and once in morning of Day 5; the first dose on each day was administered fasted). 2 participants received matching placebo.
Active
Placebo
Expérimental: Part C - KVD824 - 320 mg Fasted
12 participants were administered 320 mg of KVD824 in capsule form (1 x 320 mg capsule) on one occasion on Day 1 in a fasted state.
Active
Expérimental: Part C - KVD824 - 320 mg High fat breakfast
12 participants were administered 320 mg of KVD824 in capsule form (1 x 320 mg capsule) on one occasion on Day 1 following consumption of a high fat breakfast.
Active

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Safety - Treatment Emergent Adverse Events
Délai: Part A Days 0-10; Part B Days 0-12
Number of Subjects with Treatment Emergent Adverse Events
Part A Days 0-10; Part B Days 0-12
Safety - Vital signs
Délai: Part A: Days (-1)-10;Part B: Days (-1)-12
Number of participants with clinically significant changes in vital signs
Part A: Days (-1)-10;Part B: Days (-1)-12
Safety - Laboratory Parameters
Délai: Part A: Days (-1)-10;Part B: Days (-1)-12
Number of participants with clinically significant changes in laboratory assessments
Part A: Days (-1)-10;Part B: Days (-1)-12
Safety - ECG change in QTcF
Délai: Part A: Days (-1)-10; Part B: Days (-1)-12
Number of subjects who had any increase in QTcF parameters.
Part A: Days (-1)-10; Part B: Days (-1)-12

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Pharmacokinetic - Maximum Concentration (Cmax)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of Cmax in all cohorts of Part A, B and C.
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Time to maximum concentration (Tmax)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of Tmax for Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Terminal Elimination Rate Constant (Kel)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of Kel in Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Terminal elimination half-life (t1/2)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of t1/2 in Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Area under the concentration-time curve from time 0 to 24 hour post dose (AUC0-24)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of AUC (0-24) in Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Area under the concentration-time curve from time 0 to last measurable time-point (AUC0-t)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of AUC (0-t) in Part A and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Area under the concentration-time curve from time 0 to infinity (AUC0-inf)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of AUC (0-inf) in Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Residual Area under the curve (AUC%extrap)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of AUC%extrap in Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Apparent total body clearance (CL/F)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of CL/F in Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Apparent Volume of Distribution (Vz/F)
Délai: Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of Vz/F in Part A, Part B and Part C
Part A: Predose and up to 18 samples over a 48 hour period post dose; Part B: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5; Part C: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Area under the curve from time of first dose to 12 h post-dose (AUC0-12)
Délai: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
Evaluation of AUC0-12 in Part B
Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
Pharmacokinetic - Area under the curve from time of second dose to 12 h post-dose (AUC12-24)
Délai: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
Evaluation of AUC12-24 in Part B
Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
Pharmacokinetic - Apparent total body clearance at steady state (CLss/F)
Délai: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
Evaluation of Clss/F in Part B
Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
Pharmacokinetic - Maximum Concentration (Cmax) - Bioavailability Ratio Fed/Fasted
Délai: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of Cmax Bioavailability Ratio Fed/Fasted in Part C
Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Area under the curve from the time of dosing to the time of the last measurable concentration (AUC 0-t) - Bioavailability Fed/Fasted Ratio
Délai: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of AUC0-t Bioavailability Ratio Fed/Fasted in Part C
Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Pharmacokinetic - Area under the concentration-time curve from time 0 to infinity(AUC0-inf) - Bioavailability Fed/Fasted Ratio
Délai: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
Evaluation of AUC0-inf Bioavailability Ratio Fed/Fasted in Part C
Predose and up to 16 samples over a 24 hour period post dose per treatment period.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Directeur d'études: Study Director, KalVista Pharmaceuticals

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

12 février 2019

Achèvement primaire (Réel)

21 juin 2019

Achèvement de l'étude (Réel)

21 juin 2019

Dates d'inscription aux études

Première soumission

16 décembre 2021

Première soumission répondant aux critères de contrôle qualité

16 décembre 2021

Première publication (Réel)

5 janvier 2022

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

17 février 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

2 février 2022

Dernière vérification

1 février 2022

Plus d'information

Termes liés à cette étude

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

Essais cliniques sur KVD824

3
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