Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

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)

27 mai 2026 mis à jour par: 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.

Aperçu de l'étude

Description détaillée

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).

Type d'étude

Interventionnel

Inscription (Estimé)

320

Phase

  • Phase 4

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.

Coordonnées de l'étude

  • Nom: Tavitiya Sudjaritruk, MD, PhD
  • Numéro de téléphone: +66-53-936471
  • E-mail: tavitiya.s@cmu.ac.th

Lieux d'étude

      • Chiang Mai, Thaïlande, 50200
        • Department of Pediatrics, Faculty of Medicine, Chiang Mai University
        • Contact:

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

  • Enfant
  • Adulte

Accepte les volontaires sains

Oui

La description

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

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: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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)
Expérimental: Phase 2: Infant Acellular Pertussis-containing Vaccine Group
Infant Acellular Pertussis-containing Vaccine Group
An infant acellular pertussis (aP)-containing vaccine
Comparateur actif: Phase 2: Infant Whole-cell Pertussis-containing Vaccine Group
Infant Whole-cell Pertussis-containing Vaccine Group
An infant whole-cell pertussis (wP)-containing vaccine

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Phase 1: Maternal pertussis-neutralizing antibody geometric mean titers following TdaP2gen vaccination during pregnancy
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Chercheur principal: Tavitiya Sudjaritruk, MD, PhD, Department of Pediatrics, Faculty of Medicine, Chiang Mai University

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

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 (Estimé)

26 mai 2026

Achèvement primaire (Estimé)

31 décembre 2029

Achèvement de l'étude (Estimé)

31 décembre 2030

Dates d'inscription aux études

Première soumission

20 mai 2026

Première soumission répondant aux critères de contrôle qualité

27 mai 2026

Première publication (Réel)

2 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

2 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

27 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

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

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 .

S'abonner