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Maternal Immunization With Tetanus Toxoid, Reduced Diphtheria Toxoid, Reduced-dose (2 µg) Recombinant Pertussis Vaccine (TdaP2gen) and Its Effect on the Immune Response in Thai Infants up to 15-18 Months Old (M-PRIME)

2026年5月27日 更新者:Tavitiya Sudjaritruk、Chiang Mai University

Maternal Immunization With Tetanus Toxoid, Reduced Diphtheria Toxoid, Reduced-dose (2 µg) Recombinant Pertussis Vaccine (TdaP2gen) and Its Effect on the Immune Response to Tetanus, Diphtheria and Pertussis in Thai Infants up to 15-18 Months Old: An Open-label, Randomized Controlled Trial

Pertussis remains a major global public health problem. In Thailand, pertussis vaccination is recommended during pregnancy at 20-32 weeks' gestation, together with routine childhood diphtheria-tetanus-pertussis vaccination administered as a primary series at 2, 4, and 6 months and booster doses at 18 months and 4-6 years of age.

TdaP2gen, a newly developed combined tetanus, diphtheria, and recombinant genetically detoxified acellular pertussis vaccine containing 2 µg pertussis antigen, has shown favorable safety and non-inferior immunogenicity compared with existing pertussis vaccines. However, data on its use in pregnant women, transplacental antibody transfer, and potential immune interference in infants remain limited.

This study aims to evaluate the safety and immunogenicity of TdaP2gen in pregnant women, assess antibody transfer to newborns, and investigate immune responses to tetanus, diphtheria, and pertussis following primary and booster pertussis-containing vaccinations in infants and toddlers, including comparisons between whole-cell and acellular pertussis-containing vaccine schedules.

調査の概要

詳細な説明

Pertussis remains a major global public health problem. In Thailand, pertussis vaccination is recommended for all pregnant women at 20-32 weeks' gestation to protect newborns and young infants against pertussis during early life. In addition, combined diphtheria-tetanus-pertussis vaccination is routinely administered as a primary series at 2, 4, and 6 months of age, followed by booster doses at 18 months and 4-6 years of age.

TdaP2gen is a combined tetanus, diphtheria, and recombinant genetically detoxified acellular pertussis vaccine, containing 2 µg pertussis antigen, which has been recently developed. Previous clinical studies have demonstrated that TdaP2gen is safe and elicits non-inferior immune responses against pertussis compared with the 5 µg recombinant acellular pertussis vaccine (TdaP5gen) and the chemically inactivated Tdap vaccine. However, as TdaP2gen is a newly licensed vaccine in Thailand, data on its safety, immunogenicity in pregnant women, placental antibody transfer to infants, and potential immune interference with infant responses to routine pertussis-containing vaccines remain limited.

Therefore, this study aims to evaluate the safety and immunogenicity of TdaP2gen in pregnant women, assess transplacental antibody transfer to newborns, and investigate its impact on immune responses to diphtheria, tetanus, and pertussis following primary series and booster vaccination up to 15-18 months of age in infants and young children.

This study is divided into 3 phases as follows:

Phase 1 - Maternal and fetal phase: This phase will evaluate the immunogenicity and safety of TdaP2gen vaccination in pregnant women, including immune responses against tetanus, diphtheria, and pertussis, as well as the transplacental transfer of antibodies to newborns.

Phase 2 - Infant phase: This phase will assess immune responses to tetanus, diphtheria, and pertussis in infants following completion of the primary pertussis-containing vaccine series at 2, 4, and 6 months of age, comparing infants who receive whole-cell pertussis-containing vaccines (wP-containing vaccines) with those who receive acellular pertussis-containing vaccines (aP-containing vaccines).

Phase 3 - Toddler phase: This phase will evaluate immune responses to tetanus, diphtheria, and pertussis in toddlers after receiving a pertussis-containing booster vaccination at 15-18 months of age, comparing children who receive whole-cell pertussis-containing vaccines (wP-containing vaccines) with those who receive acellular pertussis-containing vaccines (aP-containing vaccines).

研究の種類

介入

入学 (推定)

320

段階

  • フェーズ 4

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Tavitiya Sudjaritruk, MD, PhD
  • 電話番号:+66-53-936471
  • メール:tavitiya.s@cmu.ac.th

研究場所

      • Chiang Mai、タイ、50200
        • Department of Pediatrics, Faculty of Medicine, Chiang Mai University
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人

健康ボランティアの受け入れ

はい

説明

Phase 1: Pregnant women

Inclusion Criteria:

  • Pregnant women aged 20 to 45 years
  • Healthy women in good general health
  • Gestational age between 20 and 32 weeks at enrollment
  • Singleton pregnancy
  • Low-risk, uncomplicated pregnancy as assessed by an obstetrician
  • No evidence of congenital anomalies identified on prenatal ultrasonographic screening
  • Willing to receive TdaP2gen vaccination and comply with collection of biological specimens as specified in the study protocol
  • Willing to allow their infant to receive either whole-cell pertussis-containing or acellular pertussis-containing combination vaccines according to the study randomization process, and to allow collection of biological specimens from the infant as specified in the study protocol
  • Able and willing to provide written informed consent prior to study participation

Exclusion Criteria:

  • Receipt of a tetanus-, diphtheria-, and chemical-detoxified pertussis-containing vaccine within 1 year prior to enrollment, or receipt of a tetanus-, diphtheria-, and genetic-detoxified pertussis-containing vaccine (TdaPgen) or genetic-detoxified acellular pertussis vaccine (aPgen) within 2 years prior to enrollment, including during the current pregnancy
  • History of laboratory-confirmed or clinically diagnosed pertussis infection within 1 year prior to enrollment
  • Presence of underlying medical conditions that may affect study outcomes, including but not limited to malignancy, autoimmune disease, immunodeficiency, epilepsy, hypertension, renal disease, or liver disease, as determined by the investigators
  • Pregnancy complications including hypertension (blood pressure >140/90 mmHg with proteinuria, or >150/100 mmHg regardless of proteinuria), current antihypertensive treatment, or preeclampsia
  • Endocrine disorders including hyperthyroidism, untreated hypothyroidism, or impaired glucose tolerance (e.g., type 1 or type 2 diabetes mellitus) diagnosed before or during pregnancy requiring treatment beyond dietary control
  • Severe or progressive neurological disorders, including epilepsy or a history of Guillain-Barré syndrome
  • Receipt of immunosuppressive agents, immunomodulatory agents, or high-dose systemic corticosteroids (>2 mg/kg/day, >20 mg/day, or equivalent) for more than 14 consecutive days within 6 months prior to enrollment
  • History of stillbirth, neonatal death, or recurrent spontaneous abortion (≥3 episodes).
  • Current medical or surgical treatment for prevention of preterm labor during the current pregnancy
  • Receipt of blood products, blood components, or immunoglobulins within 6 months prior to enrollment
  • Receipt of live attenuated vaccines within 3 months or any other vaccines within 28 days prior to enrollment
  • History of hypersensitivity or adverse reactions to study vaccines or vaccine components, or history of severe allergic reactions such as anaphylaxis to any vaccine
  • Behavioral, cognitive, or psychiatric conditions that, in the opinion of the investigator, may interfere with study participation or protocol compliance
  • History of smoking, alcohol abuse, or intravenous drug use that, in the opinion of the investigator, may interfere with study assessments or outcomes
  • Fever (body temperature ≥38.0°C or equivalent) within 72 hours prior to enrollment
  • Acute illness within 4 weeks prior to enrollment
  • Contraindications to intramuscular vaccination, including thrombocytopenia, coagulation disorders, hemophilia A or B, or use of anticoagulant therapy during pregnancy
  • Concurrent participation in another clinical study involving investigational vaccines or medications during participation in this study
  • Any medical or obstetric condition that, in the opinion of the study investigator, may interfere with study assessments or increase the risk to the mother or infant associated with study participation

Phase 2: Infants

Inclusion Criteria:

- All infants born to pregnant women enrolled in Phase 1 who received TdaP2gen vaccination during pregnancy will be eligible for enrollment to Phase 2 study

Exclusion Criteria:

  • Gestational age <32 weeks (very preterm birth)
  • Birth weight <1,500 grams (very low birth weight)
  • Presence of major congenital anomalies identified after birth, including congenital abnormalities associated with genetic disorders, congenital infections, or severe structural abnormalities involving major organ systems such as the central nervous system, cardiovascular system, respiratory system, hepatobiliary and gastrointestinal system, or genitourinary system
  • Presence of severe neonatal medical conditions that may affect immune responses to study vaccines, including but not limited to severe respiratory distress, severe bronchopulmonary dysplasia, hypoxic ischemic encephalopathy (HIE), severe intraventricular hemorrhage (IVH), severe sepsis, non-physiologic jaundice, neonatal autoimmune thrombocytopenia, neurological disorders such as neonatal convulsions, necrotizing enterocolitis, or intracranial hemorrhage
  • Presence of conditions associated with increased risk of serious adverse reactions to study vaccines
  • Any medical condition or circumstance that, in the opinion of the study investigator, may interfere with study assessments or increase the risk to the participant associated with study participation

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Phase 1: Maternal TdaP2gen Group
Maternal TdaP2gen Group
A combined tetanus toxoid, reduced diphtheria toxoid, reduced-dose (2 µg) genetically-detoxified recombinant acellular pertussis vaccine (TdaP2gen)
実験的:Phase 2: Infant Acellular Pertussis-containing Vaccine Group
Infant Acellular Pertussis-containing Vaccine Group
An infant acellular pertussis (aP)-containing vaccine
アクティブコンパレータ:Phase 2: Infant Whole-cell Pertussis-containing Vaccine Group
Infant Whole-cell Pertussis-containing Vaccine Group
An infant whole-cell pertussis (wP)-containing vaccine

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Phase 1: Maternal anti-pertussis toxin (PT), anti-filamentous hemagglutinin (FHA), anti-diphtheria toxoid, and anti-tetanus toxoid immunoglobulin G (IgG) geometric mean concentrations and seroresponse rates following TdaP2gen vaccination during pregnancy
時間枠:Pre-vaccination baseline, 4 weeks after vaccination (+/- 14 days), and at delivery
Assessment of maternal anti-PT, anti-FHA, anti-diphtheria toxoid, and anti-tetanus toxoid IgG geometric mean concentrations and seroresponse rates before TdaP2gen vaccination, after vaccination, and at delivery
Pre-vaccination baseline, 4 weeks after vaccination (+/- 14 days), and at delivery
Phase 1: Cord blood anti-PT, anti-FHA, anti-diphtheria toxoid, and anti-tetanus toxoid IgG geometric mean concentrations and seroresponse rates at birth
時間枠:At delivery
Assessment of anti-PT, anti-FHA, anti-diphtheria toxoid, and anti-tetanus toxoid IgG geometric mean concentrations and seroresponse rates in cord blood collected at delivery among infants born to TdaP2gen vaccinated mothers
At delivery
Phase 1: Incidence of solicited local and systemic adverse events, serious adverse events, and adverse pregnancy outcomes of TdaP2gen vaccination during pregnancy
時間枠:From vaccination until delivery, assessed up to approximately 22 weeks post-vaccination.
Assessment of solicited local and systemic adverse events as well as serious adverse events and adverse pregnancy outcomes among pregnant women receiving TdaP2gen vaccination during pregnancy.
From vaccination until delivery, assessed up to approximately 22 weeks post-vaccination.
Phase 2: Infant anti-PT, anti-FHA, anti-diphtheria toxoid, and anti-tetanus toxoid IgG geometric mean concentrations and seroresponse rates following primary diphtheria-tetanus-pertussis vaccination series
時間枠:Pre-primary series vaccination (within 2 months after birth) and post-primary series vaccination (at age 7 months +/- 14 days)
Assessment and comparison of anti-PT, anti-FHA, anti-diphtheria toxoid, and anti-tetanus toxoid IgG geometric mean concentrations and seroresponse rates between infants born to mothers receiving TdaP2gen vaccine during pregnancy who are randomized to receive either aP- or wP-containing vaccines as the primary vaccination series during infancy
Pre-primary series vaccination (within 2 months after birth) and post-primary series vaccination (at age 7 months +/- 14 days)
Phase 3: Infant anti-PT, anti-FHA, anti-diphtheria toxoid, and anti-tetanus toxoid IgG geometric mean concentrations and seroresponse rates following booster diphtheria-tetanus-pertussis vaccination
時間枠:At 12 months of age (+/- 14 days), pre-booster vaccination, and 1 month after booster vaccination (+/- 14 days)
Assessment and comparison of anti-PT, anti-FHA, anti-diphtheria toxoid, and anti-tetanus toxoid IgG geometric mean concentrations and seroresponse rates between infants born to mothers receiving TdaP2gen vaccine during pregnancy who previously received either aP or wP-containing vaccines during the primary vaccination series and subsequently receive booster vaccination at 15-18 months of age
At 12 months of age (+/- 14 days), pre-booster vaccination, and 1 month after booster vaccination (+/- 14 days)

二次結果の測定

結果測定
メジャーの説明
時間枠
Phase 1: Maternal pertussis-neutralizing antibody geometric mean titers following TdaP2gen vaccination during pregnancy
時間枠:Pre-vaccination baseline, 4 weeks after vaccination (+/- 14 days), and at delivery
Assessment of maternal pertussis-neutralizing antibody geometric mean titers in a subset of 40 pregnant women before TdaP2gen vaccination, after vaccination, and at delivery
Pre-vaccination baseline, 4 weeks after vaccination (+/- 14 days), and at delivery
Phase 1: Cord blood pertussis-neutralizing antibody geometric mean titers at birth
時間枠:At delivery
Assessment of pertussis-neutralizing antibody geometric mean titers in cord blood samples from newborns of a subset of 40 vaccinated pregnant women at delivery
At delivery
Phase 1: Knowledge and acceptability of pertussis and pertussis vaccine among pregnant women assessed using a structured questionnaire
時間枠:Pre-vaccination baseline
Assessment of knowledge and acceptability of pertussis and pertussis vaccine among pregnant women using a structured questionnaire
Pre-vaccination baseline
Phase 2: Infant pertussis-neutralizing antibody geometric mean titers following primary diphtheria-tetanus-pertussis vaccination series
時間枠:Pre-primary series vaccination (within 2 months after birth) and post-primary series vaccination (at age 7 months +/- 14 days)
Assessment and comparison of pertussis-neutralizing antibody geometric mean titers in a subset of 40 infants born to mothers receiving TdaP2gen vaccine during pregnancy who are randomized to receive either aP- or wP-containing vaccines as the primary vaccination series during infancy
Pre-primary series vaccination (within 2 months after birth) and post-primary series vaccination (at age 7 months +/- 14 days)
Phase 2: Incidence of solicited local and systemic adverse events, unsolicited adverse events, and serious adverse events following the primary diphtheria-tetanus-pertussis vaccination series in infants
時間枠:From the first dose of the primary diphtheria-tetanus-pertussis vaccination series until 1 month after completion of the primary vaccination series, assessed up to approximately 5 months
Assessment and comparison of the frequency and severity of solicited local and systemic adverse events, unsolicited adverse events, and serious adverse events following administration of aP- or wP-containing vaccines during the primary vaccination series in infants born to mothers receiving TdaP2gen vaccine during pregnancy
From the first dose of the primary diphtheria-tetanus-pertussis vaccination series until 1 month after completion of the primary vaccination series, assessed up to approximately 5 months
Phase 3: Infant pertussis-neutralizing antibody geometric mean titers following booster diphtheria-tetanus-pertussis vaccination
時間枠:At 12 months of age (+/- 14 days), pre-booster vaccination, and 1 month after booster vaccination (+/- 14 days)
Assessment and comparison of pertussis-neutralizing antibody geometric mean titers in a subset of 40 infants born to mothers receiving TdaP2gen vaccine during pregnancy who previously received either aP or wP-containing vaccines during the primary vaccination series and subsequently receive booster vaccination at 15-18 months of age
At 12 months of age (+/- 14 days), pre-booster vaccination, and 1 month after booster vaccination (+/- 14 days)
Phase 3: Incidence of solicited local and systemic adverse events, unsolicited adverse events, and serious adverse events following booster diphtheria-tetanus-pertussis vaccination in infants
時間枠:From booster vaccination through 28 days after vaccination
Assessment and comparison of the frequency and severity of solicited local and systemic adverse events, unsolicited adverse events, and serious adverse events following administration of aP or wP booster vaccination in infants born to mothers receiving TdaP2gen vaccine during pregnancy
From booster vaccination through 28 days after vaccination

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Tavitiya Sudjaritruk, MD, PhD、Department of Pediatrics, Faculty of Medicine, Chiang Mai University

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年5月26日

一次修了 (推定)

2029年12月31日

研究の完了 (推定)

2030年12月31日

試験登録日

最初に提出

2026年5月20日

QC基準を満たした最初の提出物

2026年5月27日

最初の投稿 (実際)

2026年6月2日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月2日

QC基準を満たした最後の更新が送信されました

2026年5月27日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

There is not a plan to make individual participant data (IPD) available for this study.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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