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Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetics (PKs) of ZYDPLA1 Following Oral Administration in Healthy Volunteers

2015년 12월 1일 업데이트: Zydus Lifesciences Limited

A Randomized, Double-blind, Placebo-controlled Phase I Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ZYDPLA1, a Novel DPP- IV Inhibitor, Following Oral Administration in Healthy Volunteers

This First in Human (FIH) Phase I study intends to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of ZYDPLA1 in normal healthy adult volunteers.

연구 개요

상세 설명

Glucose-dependent insulinotropic polypeptide (GIP) and Glucagon-like peptide (GLP-1) are incretin hormones, which stimulate glucose dependent insulin secretion, inhibit glucagon secretion, delay gastric emptying, suppress appetite and improve peripheral glucose uptake and disposal. Dipeptidyl peptidase-IV (DPP-IV) is a serine protease, which selectively cleaves the first two amino acids of GIP and GLP-1 thereby making it inactive. Inhibition of DPP-IV activity elevates endogenous GIP, GLP-1 and insulin levels thereby improving glucose excursion and exhibits antidiabetic activity. Since no orally active GLP-1 agonists are available, clinically orally bioavailable DPP-IV inhibitors hold great potential for the treatment of type 2 diabetes mellitus.

Cadila Healthcare Ltd. developed a novel and orally bioavailable DPP-IV inhibitor (ZYDPLA1). In-vitro studies confirm selective DPPIV inhibitory activity of the ZYDPLA1. Pre-clinical in vivo pharmacodynamic, absorption, distribution, metabolism and excretion (ADME) & toxicological studies showed the promising antidiabetic activity, good exposure and safety profile of ZYDPLA1(in various animal models).

Hence a randomized, double-blind, placebo-controlled first in man trial proposed to evaluate the safety and tolerability of ZYDPLA1 in healthy volunteers.

This study included 4 plans:

i) single dose escalation study ii) multiple dose escalation study, iii) gender effect study and iv) food effect study.

연구 유형

중재적

등록 (실제)

84

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • California
      • Chula Vista, California, 미국, 91911
        • Profil Institute for Clinical Research

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, 고령자)

건강한 자원 봉사자를 받아들입니다

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Healthy male or female between 18 and 65 years of age.
  2. Male subjects must agree to use one of the contraception methods during the study. Male contraceptive options include: Vasectomy, Abstinence requiring the use of contraceptives if becoming sexually active, or double barrier method (condom with spermicide, diaphragm or cervical cap). No Sperm donation for at least up to 90 days after last investigational product.
  3. BMI within the range 18.0 - 30.0 kg/m2 BMI value should be rounded off to one significant digit after decimal point. BMI values should be rounded to the nearest integer (ex. 30.4 rounds down to 30, while 17.5 rounds up to 18).
  4. Capable of giving written informed consent, which includes compliance with protocol.
  5. Corrected QT interval (QTc) interval < 450msec (as measured by QTcF)
  6. For gender effect study, only females with history of sterility or at least 1 year menopause or use of long acting non hormonal contraceptive measures (e.g., intrauterine device) will be recruited. Surgical sterility is defined as either bilateral tubal ligation/occlusion, bilateral oophorectomy or hysterectomy.
  7. Negative Urine drug screen including amphetamine, barbiturates, benzodiazepines, cannabinoid, cocaine, opiates, methadone and phencyclidine within 28 days prior to initiation of the study and prior to check-in.

Exclusion Criteria:

  1. Presence or history of pancreatitis at any time {Serum Amylase/Serum Lipase more than significant upper normal limit (≥1.5 times UNL)}
  2. Presence or history of severe gastrointestinal disease in the last 6 months
  3. Presence or history of renal insufficiency at any time {Serum creatinine more than upper normal limit (UNL)}
  4. Active liver disease and/or liver transaminases greater than 1.5 times UNL
  5. History or presence of other systemic disorders or diseases (e.g., respiratory, gastrointestinal, endocrine, immunological, dermatological, neurological, psychiatric disease or any other body system involvement)
  6. History or presence of any medication in the last 14 days
  7. History or presence of significant alcoholism or drug abuse within the past 1 year
  8. History or presence of significant smoking (more than 10 cigarettes per day) or consumption of tobacco products (more than 10 times per day)
  9. Difficulty with donating blood or difficulty in accessibility of veins.
  10. Intolerance to venipuncture.
  11. Systolic blood pressure more than 150 mmHg and less than 100 mmHg and diastolic blood pressure more than 90 mmHg
  12. Pulse rate less than 50/minute and more than 100/minute
  13. Any clinically significant laboratory findings during screening
  14. History or presence of any clinically significant electrocardiogram (ECG) abnormalities during screening as determined by the Principal Investigator.
  15. Major illness and/or major surgery in last 3 months
  16. Volunteers who have participated in any drug research study other than the present trial within the past 30 days (Subjected to Insurance that subject has not participated in long acting drug including new biological entities/new chemical entities/biosimilar products).
  17. Volunteers who have donated one unit (450 mL) of blood in the past 3 months
  18. Positive Alcohol breath analyzer at the time of Screening and Check-in
  19. A positive hepatitis screen (includes subtype B and C) and/or a positive test result for HIV antibody.
  20. Any food allergy, intolerance, restriction or special diet that, in the opinion of the Principal investigator or Sub-investigator, could contraindicate the study participant's participation in this study.
  21. For gender effect study, female volunteers with following criteria will not be recruited:

    • History of pregnancy or lactation in the past 3 months
    • Fertile female volunteers not protected against pregnancy by adequate long-term anti-fertility measures
    • History of less than 1 year of menopause and not using adequate long-term antifertility measures
    • Using hormonal contraceptives
    • Using hormone replacement therapy
    • Unable to give assurance for protection against pregnancy for 3 months after the participation in this trial
    • Positive urine pregnancy test on the day of check-in (women of child bearing potential)
    • Positive serum β-human chorionic gonadotropin (hCG) level at the screening visit (women of child bearing potential)

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
활성 비교기: ZYDPLA1 tablet
ZYDPLA1 tablets: Route of administration: Oral Dosage (Single Ascending Study): 1 mg, 5mg, 20mg, 50mg, 100mg, 200mg Multiple Ascending Study: 100mg, 200mg Food effect and Gender effect study: 200mg
The oral dose of ZYDPLA1 tablet administered with 240 ± 10 mL of water at ambient temperature.
위약 비교기: Placebo
Placebo tablets: Route of administration: Oral Dosage (Single Ascending Study): 1 mg, 5mg, 20mg, 50mg, 100mg, 200mg Multiple Ascending Study: 100mg, 200mg Food effect and Gender effect study: 200mg
The oral dose of placebo tablet administered with 240 ± 10 mL of water at ambient temperature.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Safety and tolerability assessed by monitoring adverse events, clinical, laboratory, electrocardiogram, and vital signs examinations.
기간: 14 Days (Plan 1, III, and IV);
14 Days (Plan 1, III, and IV);
Safety and tolerability assessed by monitoring adverse events, clinical, laboratory, electrocardiogram, and vital signs examinations.
기간: 28 Days (Plan II)
28 Days (Plan II)

2차 결과 측정

결과 측정
기간
Pharmacokinetic assessment: Maximum plasma concentration (Cmax)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Maximum plasma concentration (Cmax)
기간: 28 Days (Plan II)
28 Days (Plan II)
Time to reach maximum plasma concentration (Tmax)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Time to reach maximum plasma concentration (Tmax)
기간: 28 Days (Plan II)
28 Days (Plan II)
Area under the curve from the time of dosing to the last measurable concentration (AUC0-t)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Area under the curve from the time of dosing to the last measurable concentration (AUC0-t)
기간: 28 Days (Plan II)
28 Days (Plan II)
Area under the curve from the time of dosing to the infinity (AUC 0-inf)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Area under the curve from the time of dosing to the infinity (AUC 0-inf)
기간: 28 Days (Plan II)
28 Days (Plan II)
Terminal half life (t1/2)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Terminal half life (t1/2)
기간: 28 Days (Plan II)
28 Days (Plan II)
Elimination rate constant (λz)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Elimination rate constant (λz)
기간: 28 Days (Plan II)
28 Days (Plan II)
Clearance (CL)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Clearance (CL)
기간: 28 Days (Plan II)
28 Days (Plan II)
Volume of distribution (Vd)
기간: 14 Days (Plan I, III, and IV)
14 Days (Plan I, III, and IV)
Volume of distribution (Vd)
기간: 28 Days (Plan II)
28 Days (Plan II)
Accumulation index
기간: 28 Days (Plan II)
28 Days (Plan II)
Pharmacodynamic effect (Plan I, III, and IV) assessment by monitoring primary parameters: Plasma DPPIV
기간: 14 Days
14 Days
Pharmacodynamic effect (Plan II) assessment by monitoring primary parameters: Plasma DPPIV
기간: 28 Days
28 Days
Glucagon-like peptide-1 (active and total)
기간: 14 Days
14 Days
Glucagon-like peptide-1 (active and total)
기간: 28 Days
28 Days
Secondary parameters: Plasma glucose
기간: 14 Days
14 Days
Plasma glucose
기간: 28 Days
28 Days
Serum insulin
기간: 14 Days
14 Days
Serum insulin
기간: 28 Days
28 Days
C-peptide
기간: 14 Days
14 Days
C-peptide
기간: 28 Days
28 Days
Glucagon
기간: 14 Days
14 Days
Glucagon
기간: 28 Days
28 Days

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 책임자: Rajendrakumar H Jani, Ph.D.,, Zydus Lifesciences Limited

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

2014년 10월 1일

기본 완료 (실제)

2015년 10월 1일

연구 완료 (실제)

2015년 10월 1일

연구 등록 날짜

최초 제출

2015년 11월 24일

QC 기준을 충족하는 최초 제출

2015년 12월 1일

처음 게시됨 (추정)

2015년 12월 3일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2015년 12월 3일

QC 기준을 충족하는 마지막 업데이트 제출

2015년 12월 1일

마지막으로 확인됨

2015년 11월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • ZYDPLA1 1001

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진성 당뇨병에 대한 임상 시험

ZYDPLA1 tablet에 대한 임상 시험

구독하다