Diphtheria-Tetanus-acellular Pertussis VaccinesPhase 3NCT07596199
A Study on the Immune Response and Safety of a Combined Vaccine Against Diphtheria, Tetanus and Acellular Pertussis (dTpa) in Japanese Healthy Pregnant Women
A Phase 3 study testing dTpa in people with Diphtheria-Tetanus-acellular Pertussis Vaccines, run by GlaxoSmithKline at 21 sites in Japan.
Trial summary
The purpose of this Phase 3, non-randomized, single-arm, open-label study is to evaluate the immune response, reactogenicity and safety of GSKs dTpa vaccine in Japanese pregnant women between 27 weeks and less than 37 weeks of pregnancy. Read more about this study
- Who is it for?
- Ages 18 to 45 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Diphtheria-Tetanus-acellular Pertussis Vaccines
- What is being tested?
- dTpa
- Type of treatment
- Vaccines, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 102 participants
- Where
- 21 sitesJapan
- Study dates
- 29 Jun 2026to 31 Dec 2026
- Phase
- Phase 3
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 45 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Participants, who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
- Participants and Legally acceptable representative(s) [LAR(s)] who give physical or digital informed consent after the study has been explained according to local regulatory requirements, and before any study-specific procedures are performed. The informed consent given at screening should include consent for both the maternal participant's participation and participation of the infant after the infant's birth.
- Healthy participants as established by medical history and clinical examination at screening.
- Participants between and including 18 and 45 years of age at the time of the study intervention administration (Visit 1/Day 1).
- Pre-pregnancy body mass index (BMI) (based on participant's report) between 17.0 and 39.9 kg/m^2, inclusive.
- Pregnant female at 27,0/7 to 36,6/7 weeks of gestation (completed week 27 but not week 37) at the time of vaccination (Visit 1/Day 1), as established or confirmed by ultrasound examination.
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- No significant fetal abnormalities, as observed by the fetal morphological abnormality screening test conducted after 18 weeks of gestation and the most recent ultrasound testing (no more than 6 weeks before enrollment).
- Nuchal translucency scan, serum testing and any other prenatal tests, if conducted, should suggest normal pregnancy.
- Participants who are willing to provide cord blood and/or infant blood.
- Participants who are willing to have them and their newborns followed-up until 1 month post-delivery.
- Participants who do not plan to give their child for adoption.
- Japanese ethnic origin.
Who cannot join
- Medical conditions:
- Participants diagnosed with multiple pregnancies.
- Women with co-morbid medical or obstetric conditions that in the opinion of the investigator have the potential to complicate the pregnancy course and outcomes such as;
- Gestational hypertension (defined as systolic blood pressure >=140 mmHg and/or diastolic blood pressure >=90 mmHg) at >=20 weeks of gestation in a woman with a previously normal blood pressure. Women with gestational hypertension who maintain blood pressure in the normal range (<140 mmHg and <90 mmHg) through diet and/or on antihypertensive medications would be eligible except for eclampsia/pre-eclampsia.
- Hemodynamically significant cardiac disorders (previously corrected patent ductus arteriosis is allowed).
- Gestational diabetes which is not controlled by medication, diet and/or exercise as determined by glucose challenge/tolerance test conducted after 20 weeks of gestation or as per local recommendations of the country (Gestational diabetes is defined as absence of pre-gestational diabetes and hyperglycemia during pregnancy, which is not due to other known causes).
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- Any other conditions that in the opinion of the investigator have the potential to complicate the pregnancy course and outcomes
- Acute or unstable chronic conditions, chronic clinically significant abnormality, poorly controlled pre-existent co-morbidities or any other clinical conditions, as determined by physical examination and/or laboratory tests.
- Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination.
- Recurrent history or uncontrolled neurological disorders or any neuroinflammatory, congenital neurological conditions, encephalopathies, or seizures.
- Condition that in the judgment of the investigator would make intramuscular injection unsafe.
- Any other clinical condition that, in the opinion of the investigator, might pose additional risk to the participant and/or to the unborn infant due to participation in the clinical study.
- Prior major congenital anomalies or early onset (<34 weeks of gestation) of eclampsia/pre-eclampsia in previous pregnancy, or stillbirth or neonatal death, or multiple (>=2) spontaneous abortions, or pre-term delivery (<=34 weeks gestation) or having ongoing intervention (medical/surgical) in current pregnancy to prevent pre-term delivery.
- Family history (first degree relatives only) of congenital anomalies, recurrent pregnancy losses (two or more consecutive losses) and unexplained neonatal death(s) in the participant.
- History of an encephalopathy of unknown etiology, occurring within 7 days following previous vaccination with pertussis-containing vaccine.
- History of transient thrombocytopenia or neurological complications (for convulsions or hypotonic-hyporesponsive episodes) following an earlier immunisation against diphtheria and/or tetanus.
- History of any reaction or hypersensitivity likely to be exacerbated by any component of the study intervention or having shown signs of hypersensitivity after previous administration of diphtheria, tetanus or pertussis vaccines.
- History of physician-diagnosed or laboratory-confirmed pertussis within the past 5 years.
- Lymphoproliferative disorder or malignancy within 5 years before the study dose administration (excluding effectively treated non melanoma skin cancer).
- Prior/Concomitant therapy:
- Previous vaccination containing diphtheria, tetanus or pertussis antigens, or diphtheria and tetanus toxoids at any time during the current pregnancy and within 5 years from study participation.
- Use of any investigational or non-registered product other than the study intervention(s) during the current pregnancy or their planned use during the study period.
- Chronic administration of immune-modifying drugs (defined as more than 14 consecutive days in total) and/or planned use of long-acting immune-modifying treatments or planned administration through delivery.
- Up to 6 months prior to the study intervention administration:
- For corticosteroids, this will mean prednisone equivalent >=20 mg/day for adult participants. Inhaled, intra-articular/intra-bursal and topical steroids are allowed.
- Up to 6 months prior to the study intervention administration:
- long-acting immune-modifying drugs including among others immunotherapy monoclonal antibodies, antitumoral medication.
- Planned administration/administration of a vaccine not foreseen by the study protocol in the period starting 30 days before the dose and planned administration through delivery (Visit 3/Day of delivery), except:
- Seasonal influenza vaccines, RSV vaccines, Hepatitis B vaccines, and SARS-CoV-2, all of which may be administered according to standard of care >=14 days before or after study vaccination.
- Administration of immunoglobulins or other blood products or plasma derivatives during the period starting 3 months before the study intervention or planned administration through delivery with the exception of anti-D (Rh)-immunoglobulin.
- Planned administration of any prophylactic medication (e.g., analgesics, antipyretics) in the absence of any symptom and in anticipation of a reaction to the study intervention administration.
- Prior/Concurrent clinical study participation:
- Concurrently participating in another clinical study, at any time during the study period, in which the participant has been or will be exposed to an investigational or a non-investigational intervention drug/vaccine/invasive medical device.
- Other exclusion criteria:
- History of chronic alcohol consumption and/or drug abuse, based on investigator's judgment.
- Any study personnel or their immediate dependents, family, or household members.
Trial locations and contacts
21 sites in 1 country.
21 sites in 1 country
Japan21 sites
GSK Investigational Site
Aichi, 464-0026
GSK Investigational Site
Chiba, 279-0001
GSK Investigational Site
Chiba, 286-8520
GSK Investigational Site
Fukui, 910-0833
GSK Investigational Site
Fukuoka, 820-8505
GSK Investigational Site
Fukushima, 965-8585
GSK Investigational Site
Hokkaido, 085-8512
GSK Investigational Site
Kanagawa, 236-0004
GSK Investigational Site
Kanagawa, 251-8550
GSK Investigational Site
Kyoto, 604-8845
GSK Investigational Site
Nagano, 390-8601
GSK Investigational Site
Nara, 630-8581
GSK Investigational Site
Osaka, 556-0005
GSK Investigational Site
Osaka, 583-8588
GSK Investigational Site
Saitama, 330-0855
GSK Investigational Site
Saitama, 336-8522
GSK Investigational Site
Shizuoka, 420-8527
GSK Investigational Site
Shizuoka, 424-8636
GSK Investigational Site
Tokyo, 113-8519
GSK Investigational Site
Tokyo, 152-8902
GSK Investigational Site
Tokyo, 162-8655
About this study
Official title: A Phase 3, Non-Randomized, Single-Arm, Open-Label Study to Assess the Immunogenicity, Safety and Reactogenicity of a Single Dose of Combined Reduced-Antigen-Content Diphtheria, Tetanus and Acellular Pertussis (dTpa) Vaccine in Japanese Healthy Pregnant Women
The purpose of this Phase 3, non-randomized, single-arm, open-label study is to evaluate the immune response, reactogenicity and safety of GSKs dTpa vaccine in Japanese pregnant women between 27 weeks and less than 37 weeks of pregnancy. Both the pregnant women and their neonates born during the study will be evaluated for specific analyses.
- Being tested
- dTpa
- Keywords
- Diphtheria, tetanus and acellular pertussis (dTpa) vaccine, Pregnant women, Neonates, Immune response, Reactogenicity, Safety
- Medical subject headings
- Diphtheria, Tetanus
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
dTpaBiological
Also called Boostrix
1 dose of dTpa vaccine is administered intramuscularly.
| Study group | Role | What they receive |
|---|---|---|
| dTpa Group | Experimental | Healthy pregnant women at 27 to 36 weeks of gestation receive one dose of the investigational dTpa vaccine at Day 1 (representing the day of vaccination). Receives: Biological: dTpa |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of seropositive healthy pregnant women for anti-pertussis toxin (PT), anti-filamentous hemagglutinin (FHA) and anti-pertactin (PRN) antibodies
Seropositivity is defined as antibody concentrations (anti-PT, anti-FHA and anti-PRN) are greater than or equal to the assessed assay cut-offs. The considered cut-off values are: anti-PT: 2.693 International Units per milliliter (IU/mL), anti-FHA: 2.046 IU/mL, anti-PRN: 2.187 IU/mL, as measured by Enzyme-Linked Immunosorbent assay (ELISA).
Measured: At Month 1 post-vaccination
Number of seropositive participants for anti-PT, anti-FHA and anti-PRN antibodies from samples in cord blood sample at birth
Measured: On the Day of birth
Secondary outcomes (17)
Booster response to pertussis (PT, FHA and PRN) antigens in healthy pregnant women
Booster response to PT, FHA and PRN antigens is defined as: for participants with pre-vaccination antibody concentration below the assay cut-off, post-vaccination antibody concentration >=4 times the assay cut-off; for participants with pre-vaccination antibody concentration between the assay cut-off and below 4 times the assay cut-off, post-vaccination antibody concentration >= 4 times the pre-vaccination antibody concentration; for participants with pre-vaccination antibody concentration >=4 times the assay cut-off, post-vaccination antibody concentration >=2 times the pre-vaccination antibody concentration.
Measured: At Month 1
Antibody concentration for antibodies against pertussis (PT, FHA, PRN) in healthy pregnant women
Measured: On Day 1 (day of vaccination) and at Month 1 post-vaccination
Antibody concentration for anti-diphtheria and anti-tetanus antibodies in healthy pregnant women
Measured: On Day 1 (day of vaccination) and at Month 1 post-vaccination
Number of seroprotected healthy pregnant women for anti-diphtheria and anti-tetanus antibodies
Seroprotection is defined as antibody concentrations (anti-diphtheria and anti-tetanus) are greater than or equal to 0.1 IU/mL by ELISA test.
Measured: On Day 1 (day of vaccination) and at Month 1 post-vaccination
Antibody concentration for antibodies against pertussis (PT, FHA, PRN) in the cord blood of the neonates born to mothers that received dTpa vaccine during pregnancy
Measured: On the Day of birth
Antibody concentration for anti-diphtheria and anti-tetanus antibodies in cord blood of the neonates born to mothers that received dTpa vaccine during pregnancy
Measured: On the Day of birth
Number of seroprotected neonates for anti-diphtheria and anti-tetanus antibodies, from samples in cord blood
Measured: On the Day of birth
Number of healthy pregnant women with solicited administration site adverse events
The assessed events are pain, redness and swelling.
Measured: From Day 1 (day of vaccination) to Day 7 post-vaccination
Number of healthy pregnant women with solicited systemic adverse events (AEs)
The assessed events are arthralgia, gastrointestinal symptoms, fatigue, fever, headache and myalgia. Fever is defined as temperature >=37.5 degrees Celsius.
Measured: From Day 1 (day of vaccination) to Day 7 post-vaccination
Number of healthy pregnant women with unsolicited adverse events
An unsolicited AE is an AE that was either not included in the list of solicited AEs or could be included in the list of solicited AEs but with an onset outside the specified period of follow-up for solicited AEs. Unsolicited AEs include both serious and non-serious AEs.
Measured: From Day 1 (day of vaccination) to Day 30 post-vaccination
Number of healthy pregnant women with serious adverse events (SAEs)
An SAE is defined as any untoward medical occurrence that, at any dose, results in death, is life threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect in the offspring of a study participant, abnormal pregnancy outcomes, is a suspected transmission of any infectious agent via an authorized medicinal product, or other situations as per investigator's judgment.
Measured: From Day 1 (day of vaccination) and up to 1-month post-delivery (study end)
Number of healthy pregnant women with AEs and SAEs leading to study withdrawal
Measured: From the Day 1 (day of vaccination) and up to 1-month post-delivery (study end)
Number of healthy pregnant women with pregnancy outcomes at delivery
The assessed pregnancy outcomes are: live birth with congenital anomalies, still birth with no congenital anomalies, still birth with congenital anomalies, elective termination with no congenital anomalies, elective termination with congenital anomalies.
Measured: On the Day of delivery
Number of healthy pregnant women with pregnancy-related AEs
The assessed pregnancy-related AEs are (but not limited to): gestational diabetes, pregnancy-related hypertension, pre-eclampsia, eclampsia, premature rupture of membranes, preterm premature rupture of membranes, premature labor, threatened premature labor, fetal growth restriction, obstetrical hemorrhage, maternal death.
Measured: From Day 1 (day of vaccination) and up to 1-month post-delivery
Number of neonates, born to mothers that received dTpa vaccine during pregnancy, with neonatal AEs
The assessed neonatal AEs are (but not limited to): preterm birth, neonatal death, small for gestational age, neonatal hypoxic ischemic encephalopathy, failure to thrive/growth deficiency.
Measured: From the Day of birth and up to 1-month post-birth
Number of neonates, born to mothers that received dTpa vaccine during pregnancy, participants with SAEs
Measured: From the Day of birth and up to 1-month post-birth
Number of neonates, born to mothers that received dTpa vaccine during pregnancy, with AEs and SAEs leading to study withdrawal
Measured: From the Day of birth and up to 1-month post-birth
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 May 2026
- Study start29 Jun 2026
- Primary completion23 Nov 2026 (estimated)
- Study completion31 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Diphtheria-Tetanus-acellular Pertussis VaccinesStudies of the same condition, open and under way.
- More trials run by GlaxoSmithKlineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Prevention
- Allocation
- Non-randomised
- Intervention model
- Single group
- Model description
- Non-randomized, single-arm, open-label
- Masking
- None (open label)
- Enrolment
- 102 participants (actual)
Sponsor and investigators
- Lead sponsor
- GlaxoSmithKline
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07596199
- Sponsor's protocol ID
- 308736
- Status last verified
- Sep 2026
- First submitted
- 13 May 2026
- Last updated
- 8 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Study Sponsor will assess requests from qualified researchers for anonymized individual patient-level data and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.gsk-studyregister.com/gsk-patient-level-data-sharing-july2025.pdf