- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT05178355
A Single and Multiple Doses Safety, Tolerability, Pharmacokinetics and Food Effect Study of KVD824 in Healthy Volunteers
2022년 2월 2일 업데이트: 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.
연구 개요
상세 설명
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.
연구 유형
중재적
등록 (실제)
108
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Merthyr Tydfil, 영국
- KalVista Investigative Site
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
18년 (성인)
건강한 자원 봉사자를 받아들입니다
예
연구 대상 성별
남성
설명
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.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 크로스오버 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
Placebo
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실험적: 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.
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Active
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실험적: 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.
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Active
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Safety - Treatment Emergent Adverse Events
기간: Part A Days 0-10; Part B Days 0-12
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Number of Subjects with Treatment Emergent Adverse Events
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Part A Days 0-10; Part B Days 0-12
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Safety - Vital signs
기간: Part A: Days (-1)-10;Part B: Days (-1)-12
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Number of participants with clinically significant changes in vital signs
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Part A: Days (-1)-10;Part B: Days (-1)-12
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Safety - Laboratory Parameters
기간: Part A: Days (-1)-10;Part B: Days (-1)-12
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Number of participants with clinically significant changes in laboratory assessments
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Part A: Days (-1)-10;Part B: Days (-1)-12
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Safety - ECG change in QTcF
기간: Part A: Days (-1)-10; Part B: Days (-1)-12
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Number of subjects who had any increase in QTcF parameters.
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Part A: Days (-1)-10; Part B: Days (-1)-12
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Pharmacokinetic - Maximum Concentration (Cmax)
기간: 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.
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Evaluation of Cmax in all cohorts of Part A, B and C.
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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.
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Pharmacokinetic - Time to maximum concentration (Tmax)
기간: 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.
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Evaluation of Tmax for Part A, Part B and Part C
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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.
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Pharmacokinetic - Terminal Elimination Rate Constant (Kel)
기간: 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.
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Evaluation of Kel in Part A, Part B and Part C
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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.
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Pharmacokinetic - Terminal elimination half-life (t1/2)
기간: 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.
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Evaluation of t1/2 in Part A, Part B and Part C
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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.
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Pharmacokinetic - Area under the concentration-time curve from time 0 to 24 hour post dose (AUC0-24)
기간: 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.
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Evaluation of AUC (0-24) in Part A, Part B and Part C
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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.
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Pharmacokinetic - Area under the concentration-time curve from time 0 to last measurable time-point (AUC0-t)
기간: 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.
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Evaluation of AUC (0-t) in Part A and Part C
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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.
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Pharmacokinetic - Area under the concentration-time curve from time 0 to infinity (AUC0-inf)
기간: 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.
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Evaluation of AUC (0-inf) in Part A, Part B and Part C
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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.
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Pharmacokinetic - Residual Area under the curve (AUC%extrap)
기간: 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.
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Evaluation of AUC%extrap in Part A, Part B and Part C
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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.
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Pharmacokinetic - Apparent total body clearance (CL/F)
기간: 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.
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Evaluation of CL/F in Part A, Part B and Part C
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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.
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Pharmacokinetic - Apparent Volume of Distribution (Vz/F)
기간: 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.
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Evaluation of Vz/F in Part A, Part B and Part C
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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.
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Pharmacokinetic - Area under the curve from time of first dose to 12 h post-dose (AUC0-12)
기간: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
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Evaluation of AUC0-12 in Part B
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Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
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Pharmacokinetic - Area under the curve from time of second dose to 12 h post-dose (AUC12-24)
기간: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
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Evaluation of AUC12-24 in Part B
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Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
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Pharmacokinetic - Apparent total body clearance at steady state (CLss/F)
기간: Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
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Evaluation of Clss/F in Part B
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Pre-dose and up to 11 samples over a 24 hour period post morning dose, day 1 and 5
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Pharmacokinetic - Maximum Concentration (Cmax) - Bioavailability Ratio Fed/Fasted
기간: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
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Evaluation of Cmax Bioavailability Ratio Fed/Fasted in Part C
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Predose and up to 16 samples over a 24 hour period post dose per treatment period.
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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
기간: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
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Evaluation of AUC0-t Bioavailability Ratio Fed/Fasted in Part C
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Predose and up to 16 samples over a 24 hour period post dose per treatment period.
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Pharmacokinetic - Area under the concentration-time curve from time 0 to infinity(AUC0-inf) - Bioavailability Fed/Fasted Ratio
기간: Predose and up to 16 samples over a 24 hour period post dose per treatment period.
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Evaluation of AUC0-inf Bioavailability Ratio Fed/Fasted in Part C
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Predose and up to 16 samples over a 24 hour period post dose per treatment period.
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
수사관
- 연구 책임자: Study Director, KalVista Pharmaceuticals
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
2019년 2월 12일
기본 완료 (실제)
2019년 6월 21일
연구 완료 (실제)
2019년 6월 21일
연구 등록 날짜
최초 제출
2021년 12월 16일
QC 기준을 충족하는 최초 제출
2021년 12월 16일
처음 게시됨 (실제)
2022년 1월 5일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2022년 2월 17일
QC 기준을 충족하는 마지막 업데이트 제출
2022년 2월 2일
마지막으로 확인됨
2022년 2월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
KVD824에 대한 임상 시험
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KalVista Pharmaceuticals, Ltd.완전한
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KalVista Pharmaceuticals, Ltd.종료됨혈관부종, 유전성, 유형 I 및 II미국, 체코, 독일, 헝가리, 이탈리아, 북 마케도니아, 영국, 호주, 불가리아, 캐나다, 프랑스, 뉴질랜드, 푸에르토 리코