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Safety and Immunogenicity of a Combined Diphtheria, Tetanus, Whole Cell Pertussis, Hepatitis B, Recombinant Poliomyelitis and Haemophilus Influenzae Type b (Hib) Vaccine (SIIPL DTwP-HepB-rPV-Hib)

2026년 10월 5일 업데이트: Serum Institute of India Pvt. Ltd.

A Phase I/II, Double-Blind, Randomized, Active Controlled, Multi-centric Clinical Trial to Assess the Reactogenicity, Safety and Immunogenicity of a Combined Diphtheria, Tetanus, Whole Cell Pertussis, Hepatitis B, Recombinant Poliomyelitis and Haemophilus Influenzae Type b (Hib) Vaccine (SIIPL DTwP-HepB-rPV-Hib) in Comparison With HEXASIIL® (DTwP-HepB-IPV-Hib) Vaccine in Healthy Toddlers and Infants.

This is a Phase I/II, double-blind, randomized, active controlled, multi-centric clinical trial to assess the reactogenicity, safety and immunogenicity of a SIIPL DTwP-HepB-rPV-Hib vaccine in comparison with HEXASIIL® in healthy toddlers and infants. This trial is planned as a Phase I/II trial with two age cohorts to be enrolled sequentially, starting with healthy toddlers and subsequently extending to healthy infants.

In Phase I of the trial, after at least one parent signs the informed consent and the participant's eligibility is confirmed, healthy toddlers aged 12-24 months will be randomized in a 2:1 ratio, to receive 0.5 mL of either of the vaccines intramuscularly in the upper anterolateral aspect of the thigh. Following vaccination, all toddlers will be observed at the site for minimum 30 (+15) minutes for any Iimmediate Adverse Event (IAE). Solicited Adverse Events (AEs) will be actively collected for 7 days post vaccination. Unsolicited AEs and Serious AEs will be collected throughout the trial from the time of signing informed consent till 28 days post vaccination. Blood samples for immunogenicity assessment will be obtained from all participating toddlers at Visit 1 (Prior to vaccination) and at Visit 4.

A Data Safety Monitoring Board (DSMB) meeting will be convened for the evaluation of 7-day safety data in all participants. The DSMB shall review the safety data and provide recommendations to initiate Phase II of the trial. Additionally, Safety Review Comitte (SRC) will review the 24-hour safety data from the initial sentinel group (three participants) and give advice on progression to the subsequent enrolment in Phase I.

After at least one parent signs the informed consent and the participant's eligibility is confirmed, all infants will be randomized in 2:1 ratio to receive a 3-dose primary vaccination series at 6, 10 and 14 weeks of age. Each participant will receive 0.5 mL of either vaccine intramuscularly in the upper anterolateral aspect of the thigh. Following each vaccination, all infants will be observed at the site for minimum 30 (+15) minutes for any IAEs. Active follow up for solicited AEs will be conducted over the 7-day period after each vaccination. Unsolicited AE/SAEs will be collected from signing of informed consent till Visit 10. Blood samples for immunogenicity assessment will be obtained from all participating infants at Visit 1 (Prior to vaccination) and at Visit 10.

연구 개요

연구 유형

중재적

등록 (추정된)

186

단계

  • 2 단계
  • 1단계

연락처 및 위치

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

연구 연락처

연구 연락처 백업

연구 장소

      • Dhaka, 방글라데시, 1212
        • International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)
        • 연락하다:
        • 수석 연구원:
          • K. Zaman, MD

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

1개월 (어린이)

건강한 자원 봉사자를 받아들입니다

예

연구 대상 성별

모두

설명

Inclusion Criteria:

Phase 1

  1. Male or female toddlers aged between 12-24 (both inclusive) months on the day of vaccination, who have completed primary immunization series against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis (Oral Polio Vaccine [OPV] and/or Inactivated Polio Vaccine [IPV]) and Haemophilus influenzae type b at least 6 months prior to enrolment and have not received the booster dose for the above-mentioned vaccines.
  2. Toddlers in good health, as determined by their medical history, physical examination and the clinical judgment of the Investigator.
  3. Toddlers with weight-for-length z-score is ≥ -2 Standard Deviation (SD) at the time of enrolment.
  4. Toddler's parent(s) willingness and ability to comply with the requirements of the protocol.
  5. Informed consent signed by at least one parent.

Phase 2

  1. Male or female infants aged 6-8 weeks at the time of first vaccination.
  2. Infants with good health, as determined by the medical history, physical examination and clinical judgment of the Investigator.
  3. Infants who are OPV naive.
  4. Informed consent form signed by at least one parent.
  5. Infants born at full term pregnancy (≥ 37 weeks).
  6. Infants with weight-for-length z-score ≥ -2 SD at the time of enrolment.
  7. Willingness of participant's parent(s) to comply with the requirements of the protocol.

Exclusion Criteria:

Phase 1

  1. History of diphtheria/tetanus/pertussis/hepatitis B/Haemophilus influenzae type b/poliomyelitis infection(s).

  2. Presence of fever ≥ 38°C/100.4°F within 48 hours.

  3. Acute illness of moderate to severe intensity according to the clinical judgment of the investigator.

  4. History of administration of any investigational or non-registered product (drug or vaccine) within 4 weeks prior to administration of IMPs or planned during the course of trial participation.

  5. Administration of any vaccine (except OPV during government immunization campaign) in the 4 weeks preceding the IMP administration or planned receipt of any vaccine during the trial participation period.

  6. History of anaphylaxis, or any serious vaccine reaction, or hypersensitivity/allergy to any vaccine or components of IMPs.

  7. History of following events that are known to have occurred in temporal relation to receipt of pertussis-containing vaccine:

    • temperature ≥40°C within 48 hours of vaccination, not due to another identifiable cause.
    • collapse or shock-like state (hypotonic-hyporesponsiveness episode) within 48 hours of vaccination.
    • persistent, inconsolable crying lasting ≥ 3 hours, occurring within 48 hours of vaccination.
  8. History of major congenital defects or developmental disorders or genetic diseases as determined by medical history or clinical assessment.

  9. History of thrombocytopenia or a bleeding disorder following IM administration.

  10. History or current evidence of any clinically significant chronic disease that in the opinion of the Investigator might interfere with the evaluation of trial objectives.

  11. Receipt of a blood transfusion, other blood products, or immunoglobulins in 3 months prior to IMP administration, or planned administration during the active trial period.

  12. Receipt of antibiotics in the past 3 days.

  13. Family history of any medical conditions, that in the investigator's opinion, could affect the trial outcomes.

  14. Presence of evolving or changing neurological disorder or toddler with a history of seizures and/or encephalopathy.

  15. Known personal or maternal history of Human Immunodeficiency Virus (HIV), Hepatitis B or Hepatitis C seropositivity.

  16. Planned surgery during the trial.

  17. Toddlers with a known or suspected impairment of the immune function, or those receiving immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy or received immunosuppressive therapy within 3 months prior to entry in the trial.

  18. Participation in another clinical trial 4 weeks preceding the trial enrolment or planned participation during the present trial period in another clinical trial.

  19. Toddlers whose families are planning to leave the area of the trial site before the end of the trial period.

Phase 2

  1. History of diphtheria/tetanus/pertussis/hepatitis B/Haemophilus influenzae type b/poliomyelitis infection(s).
  2. Presence of fever ≥ 38°C/100.4°F within 48 hours.
  3. Previous vaccination or planned receipt of any vaccine against diphtheria, tetanus, pertussis, hepatitis B (except birth dose), poliomyelitis or Haemophilus influenzae type b infection apart from IMPs during the trial period.
  4. Acute illness of moderate to severe intensity according to the clinical judgment of the investigator.
  5. Administration of any vaccine in the 4 weeks (except BCG) preceding the first dose of IMP administration.
  6. Receipt of antibiotics in the past 3 days.
  7. History of major congenital defects or illness that require medical therapy, as determined by medical history or clinical assessment.
  8. History of any clinically significant chronic disease that in the opinion of the Investigator, might interfere with the evaluation of the trial objectives.
  9. History of anaphylaxis, or any serious vaccine reaction, or hypersensitivity/allergy to any vaccine or components of IMP.
  10. Infants with a known or suspected impairment of the immune function, or those receiving immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy or received immunosuppressive therapy prior to trial entry.
  11. Presence of evolving or changing neurological disorder or infant with a history of seizures and/or encephalopathy.
  12. Known thrombocytopenia or a bleeding disorder.
  13. Planned surgery during the trial.
  14. Known personal or maternal history of HIV, Hepatitis B or Hepatitis C seropositivity.
  15. Receipt of blood or blood-derived products or immunoglobulins or planned administration during the trial which might interfere with the assessment of the immune response.
  16. Participation in another clinical trial 4 weeks preceding the trial enrolment or planned participation during the present trial period in another clinical trial.
  17. Infants whose families are planning to leave the area of the trial site before the end of the trial period.

공부 계획

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

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 방지
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Hexavalent (DTwP-HepB-rPV-Hib) Vaccine

Hexavalent (DTwP-HepB-rPV-Hib) Vaccine for active immunization of infants and toddlers

Hexavalent (DTwP-HepB-rPV-Hib) Vaccine

활성 비교기: HEXASIIL

Hexavalent (DTwP-HepB-IPV-Hib) Vaccine for active immunization of infants and toddlers

Hexavalent (DTwP-HepB-IPV-Hib) Vaccine

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
The incidence, severity and relationship of solicited AEs occurring up to 7 days following vaccination, unsolicited AEs and Serious Adverse Events till 28 days following vaccination in toddlers
기간: 28 days
28 days
The incidence, severity and relationship of solicited AEs occurring up to 7 days following each vaccination, unsolicited AEs and SAEs till 28 days post completion of a 3-dose primary vaccination series in infants
기간: 28 days post last dose
28 days post last dose

2차 결과 측정

결과 측정
기간
Percentage of toddlers achieving seroprotection for diphtheria, tetanus, hepatitis B, Haemophilus influenzae type b, poliovirus types 1, 2 & 3 and seroconversion/seropositivity for pertussis and, 28 days following vaccination
기간: 28 days
28 days
Percentage of infants achieving seroprotection for diphtheria, tetanus, hepatitis B, Hib, seroprotection and seroconversion for poliovirus types 1, 2 & 3 and seroconversion/seropositivity for pertussis and, 28 days post completion of 3 doses.
기간: 28 days after last dose
28 days after last dose
Geometric mean concentrations/titres (GMCs/GMTs) of anti-diphtheria, anti-tetanus, anti-pertussis, anti-HBsAg, anti-PRP (polyribosyl ribitol phosphate) and anti-polio types 1, 2 & 3 antibodies, 28 days following vaccination in toddlers
기간: 28 days
28 days
Geometric mean concentrations/titres (GMCs/GMTs) of anti-diphtheria, anti-tetanus, anti-pertussis, anti-HBsAg, anti-PRP and anti-polio types 1, 2 & 3 antibodies, 28 days post completion of a 3-dose primary vaccination series in infants.
기간: 28 days after last dose
28 days after last dose

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 책임자: Hitt Sharma, Serum Institute of India Pvt. Ltd.

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 (추정된)

2026년 10월 1일

기본 완료 (추정된)

2027년 10월 1일

연구 완료 (추정된)

2027년 10월 1일

연구 등록 날짜

최초 제출

2026년 9월 21일

QC 기준을 충족하는 최초 제출

2026년 9월 29일

처음 게시됨 (실제)

2026년 10월 2일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 6일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 5일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

키워드

추가 관련 MeSH 약관

기타 연구 ID 번호

  • SII-rPV-wHEXA-02

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

Summary results

IPD 공유 액세스 기준

Researchers who provide a methodologically sound proposal may be provided the access after Sponsor permission and if signed data-access agreements are in place.

IPD 공유 지원 정보 유형

  • 연구_프로토콜

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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. .

구독하다