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Transmission-Blocking Vaccine Pvs230D1-EPA/Matrix-M in Healthy Malaria-Naive Adults Using a Plasmodium Vivax Controlled Human Malaria Infection and Transmission Model

Phase 1/2 Study of Transmission-Blocking Vaccine Pvs230D1-EPA/Matrix-M in Healthy Malaria-Naive Adults Using a Plasmodium Vivax Controlled Human Malaria Infection and Transmission Model

Background:

Malaria is a disease caused by parasites spread by mosquito bites. Researchers want to test a vaccine that could stop mosquitoes from picking up these parasites when they bite infected people. This could stop malaria from spreading.

Objective:

To test a study vaccine (Pvs230D1-EPA/MM) to stop malaria transmission in healthy adults.

Eligibility:

Healthy people aged 18 to 54 years. People who already received the vaccine during a different study are also needed.

Design:

Participants will be screened. They will have a physical exam. They will have blood tests and a test of their heart function (a simple electrocardiogram or EKG).

The vaccine is given as an injectionin the upper arm. Participants who have never gotten the study vaccine will get 3 vaccines; each injection will be about 1 month apart. Participants who were vaccinated before will receive only 1 vaccine for this study. All participants will have multiple phone and in-person follow-up visits after each vaccination.

Two to 12 weeks after their last vaccine, all participants will be injected with live malaria parasites. Then they will be seenin the clinic for about 3 days. They will be monitored daily until they develop symptoms of malaria, usually in about 10 days then will be admitted to the NIH hospital.

While in the NIH hospital, participants will have 3 mosquito feedings: Two cups containing mosquitoes will be placed on an arm or leg. The mosquitoes will feed for about 15 minutes. Participants will receive medicines to relieve discomfort from the bites.

Participants will then be treated for malaria. They will have follow-up visits and calls until they fully recover.

Panoramica dello studio

Descrizione dettagliata

Study Description:

This is a single-site, phase 1/2 study of Pvs230D1-EPA/MM and bloodstage controlled human malaria infection and transmission (CHMI-T) model in healthy malaria-naive adults at the NIH Clinical Center (NIHCC), to assess the safety, reactogenicity, and efficacy of Pvs230D1-EPA/Matrix- M (MM). Three doses of the primary vaccine series will be administered at 1-month intervals (study days 0, 28, and 56) to those who are vaccine naive. Concurrently, a fourth (booster) dose will be given to participants who previously received the primary vaccine series while enrolled in NIH protocol 001501, Phase 1 dose escalation study of the Plasmodium vivax transmission-blocking vaccine Pvs230D1-EPA/Matrix-M to assess safety, immunogenicity, and transmission-blocking activity in healthy malaria-naive adults. Two to twelve weeks after the final vaccination, challenge agent derived from a cell bank of cryopreserved blood-stage P. vivax (PvHMB-CCE001) will be administered intravenously (IV). Participants will be monitored and admitted to the NIHCC to undergo safety monitoring, transmission assays, and receive antimalarial treatment. Participants enrolled on NIH protocol 001970, Induced blood-stage malaria in healthy malaria-naive adults to assess the safety and infectivity of Plasmodium vivax challenge agent and evaluate transmission in mosquito feeding assays , will serve as open-label controls. This group includes 10 nonconcurrent controls and 10 controls who will undergo challenge concurrently to vaccinees.

Objectives:

Primary Objectives:

  • To assess the safety and reactogenicity of Pvs230D1-EPA/MM primary vaccine series in healthy malaria-naive adults.
  • To assess efficacy of Pvs230D1-EPA/MM vaccine using the CHMI-T model.

Secondary Objectives:

  • To assess the safety and reactogenicity of Pvs230D1-EPA/MM booster vaccine in healthy malaria-naive adults.
  • To determine the antibody response to Pvs230D1-EPA/MM primary vaccine series and booster dose.
  • To assess functional activity of Pvs230D1-EPA/MM primary vaccine series and booster vaccine using the CHMI-T model.
  • To assess the safety of CHMI-T.

Exploratory Objectives:

  • To assess host responses to P. vivax CHMI-T.
  • To assess blood- and sexual-stage parasite growth profiles during P. vivax CHMI-T.
  • To assess cellular and transcriptomic responses to Pvs230D1- EPA/MM.

Endpoints:

Primary Endpoints:

  • Incidence of immediate adverse events (AEs) within 30 minutes following each vaccine dose.
  • Incidence and severity of local and systemic AEs within 14 days following each vaccine dose.
  • Incidence of serious adverse events (SAEs) for the entire study duration.
  • Transmission of P. vivax to Anopheles spp. using direct skin feeding (DSF) assay as determined by the detection and quantification of oocysts following midgut dissection.

Secondary Endpoints:

  • Incidence of immediate AEs within 30 minutes following booster vaccine.
  • Incidence and severity of local and systemic AEs within 14 days following booster vaccine.
  • Incidence of SAEs following booster vaccine for the entire study duration.
  • Anti-Pvs230D1 antibody levels and durability of immune response, as measured by enzyme-linked immunosorbent assay (ELISA), at various timepoints.
  • Transmission of P. vivax to Anopheles spp. using membrane feeding assays as determined by the detection and quantification of oocysts following midgut dissection and/or other methods.
  • Incidence and severity of CHMI-T-related local and systemic AEs or SAEs from challenge administration and through mosquito procedures, until 34 days post-challenge agent inoculation.

Exploratory Endpoints:

  • Antibody levels elicited following CHMI-T (e.g., ELISA levels), to various stage-specific P. vivax antigens.
  • Asexual blood-stage and sexual stage parasite growth profiles by quantitative polymerase chain reaction (qPCR) and/or microscopy.
  • Collection of P. vivax containing blood, including gametocytes, for use in mosquito transmission assays and other studies, such as parasite biology studies.
  • Cellular immune responses to vaccination and infection.
  • Host response profiles (e.g. whole genome transcriptional profiling)
  • Isolation and characterization of antigen-reactive B cells, including B cell receptor (BCR) sequencing.

Tipo di studio

Interventistico

Iscrizione (Stimato)

220

Fase

  • Fase 2
  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Maryland
      • Bethesda, Maryland, Stati Uniti, 20892
        • National Institutes of Health Clinical Center
        • Contatto:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • Numero di telefono: TTY dial 711 (800) 411-1222
          • Email: ccopr@nih.gov
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 54 anni (Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

  • INCLUSION CRITERIA:

All Participants

In order to participate in this study, an individual must meet all of the following criteria:

  • Age >=18 and <=54 years at the time of enrollment in this protocol, or for booster participants, at the time of enrollment into NIH protocol 001501.
  • In good general health and without clinically significant medical history.
  • Able to provide informed consent.
  • Study comprehension exam passed (a score of >=80% or per investigator's discretion) prior to study activities.
  • Individuals of childbearing potential must agree to use an acceptable method of contraception from 1 month prior to day 0 to 1 month after completion of anti-malarial treatment. Participants who receive only the booster vaccination need only agree to use contraception from 1 month prior to day 0 to 1 month after the booster vaccination.

Acceptable methods of contraception include the following:

  • A barrier method (e.g., consistent condom use) combined with an oral contraceptive pill, hormonal patch, or ring.
  • Parenteral hormonal contraceptive implant or an intrauterine device.

Participants who otherwise are not at risk of becoming pregnant, at the judgement of the investigator will not be required to use contraception. Such participants may include those:

  • Having undergone hysterectomy, bilateral oophorectomy, or bilateral fallopian tube ligation.

  • Having reached menopause (age >=45 years plus no menses for 12 consecutive months without an alternative medical cause).

  • Having exclusive same-sex relations or committed longstanding abstinence due to a serious life choice.

  • Having an exclusive male partner who has undergone vasectomy at least 4 months prior.

    • Suitable accommodation and reliable access to the NIHCC for the duration of the study, in the opinion of the investigator.
    • Willing to allow long-term storage of study samples for future research.

Primary Vaccine Series with CHMI-T Participants

In order to participate in this study an individual must meet all of the following criteria:

  • RBCs positive for Duffy antigen/chemokine receptor.
  • Willing to refrain from donating blood throughout the study until 3 years after completion of anti-malarial treatment.

Booster Vaccine Participants

In order to participate in this study an individual must meet all of the following criteria:

  • Has received all 3 doses of the primary vaccine series as a part of NIH protocol 001501 with the 3rd dose occurring no less than 12 months prior to intended enrollment.
  • Willing to refrain from donating blood throughout the study until 6 months after the booster vaccination.

The following additional criteria must be met in order to for participants to undergo optional CHMI-T:

  • Willing to refrain from donating blood throughout the study until 3 years after completion of anti-malarial treatment.
  • RBCs positive for Duffy antigen/chemokine receptor.

EXCLUSION CRITERIA:

All Participants

An individual who meets any of the following criteria will be excluded from participation in this study:

  • Planned travel to a malaria-endemic area (see https://www.cdc.gov/malaria/travelers/country_table/a.html) until 6-months beyond the final vaccination.

    --Exceptions may be made, at the investigator s discretion, if the travel is limited to areas without appreciable levels of P. vivax transmission.

  • History of travel to or residence in a P. vivax malaria endemic region for more than 2 weeks during the past 2 years.

  • Any prior confirmed P. vivax malaria diagnosis or clinical history consistent with P. vivax malaria diagnosis within the previous 5 years, at the investigator s discretion.

  • For individuals of childbearing potential:

    • Currently breastfeeding.
    • Currently pregnant as determined by history or a positive human choriogonadotropin (beta-hCG) test, urine or serum.
    • Planning to become pregnant in the next 12 months.
  • History of anaphylaxis, severe allergy, or other concerning adverse reaction, in the opinion of the investigator, to a previous vaccine.

  • Any individual without good peripheral venous access, at the investigator s discretion.

  • Being a current or former study team member or clinical trial staff with direct involvement of the trial or being an employee supervised by a study team member.

  • Any of the following within the specified periods:

    • Chronic systemic immunosuppressive medications (>14 days) within 6 months of study day 0 (e.g., cytotoxic medications, adrenocorticotrophic hormone, or oral/parental corticosteroids equivalent to >0.5 mg/kg/day of prednisone).
    • Investigational or non-FDA approved/authorized product or vaccine within 28 days prior to study day 0, or
    • Prior receipt of packed red cells or other blood products or immunoglobulins within 6 months of study day 0, or
    • Receipt of any vaccination less than 28 days before day 0.
  • Clinically significant medical condition, physical examination findings, other clinically significant abnormal laboratory results, or past medical history including:

    • Screening blood test laboratory parameters outside of local lab normal range.

      • Individuals may be included at the investigator s discretion for not clinically significant values outside of normal range.
      • In the event of abnormal test results, confirmatory repeat tests will be requested, at the investigator s discretion.
    • HIV, hepatitis B, and/or hepatitis C as determined by HIV antigen/antibody, Hepatitis B surface antigen, and anti-Hepatitis C antibody laboratory tests, respectively.

    • Immunodeficiency including asplenia or functional asplenia or significant autoimmune disease.

  • Investigational P. vivax malaria vaccine within the last 2 years with the exception of Pvs230D1-EPA/MM as part of NIH protocol 001501.

  • Any other finding that, in the judgment of the investigator, would interfere with, or serve as a contraindication to, protocol adherence, assessment of safety or reactogenicity, or a participant s ability to give informed consent, or increase the risk of having an adverse outcome from participating in the study.

Primary Vaccine Series Participants

An individual who meets any of the following criteria will be excluded from participation in this study:

  • For individuals of childbearing potential:

    --Rh blood group negative.

  • History of a severe reaction to arthropod bites, or history of anaphylaxis or severe unexpected allergy to any substance.

  • Clinically significant medical condition, physical examination findings, other clinically significant abnormal laboratory results, or past medical history including:

    • Retinal disease, visual field changes, psoriasis, porphyria, or known allergy to chloroquine or artemether/lumefantrine.
    • Cardiac disease including >10% cardiovascular risk as determined by the nonlaboratory method described by Gaziano or an abnormal EKG demonstrating a corrected QT interval by Fridericia s (QTcF) formula of >450 msec or other concerning arrhythmia.
  • Current or planned use of medications known to significantly prolong the QT interval or otherwise interfere with study agents.

  • Smoking more than 5 cigarettes or equivalent per day and unable to stop smoking for the duration of admission. Participants may smoke up to 5 cigarettes or equivalent per day for the rest of the study (by attestation), at investigators discretion.

  • History of alcohol use disorder (exceptions may be made at the investigator s discretion if they have completed treatment or are otherwise currently abstinent) or refusal to agree to refrain from drinking from the day of the challenge agent inoculation until completion of their antimalarial course.

Booster Vaccine Participants

An individual who meets any of the following criteria will be excluded from participation in the optional CHMI-T component of the study:

  • For individuals of childbearing potential:

    --Rh blood group negative.

  • History of a severe reaction to arthropod bites, or history of anaphylaxis or severe unexpected allergy to any substance.

  • Clinically significant medical condition, physical examination findings, other clinically significant abnormal laboratory results, or past medical history including:

    • Retinal disease, visual field changes, psoriasis, porphyria, or known allergy to chloroquine or artemether/lumefantrine.
    • Cardiac disease including >10% cardiovascular risk as determined by the nonlaboratory method described by Gaziano or an abnormal EKG demonstrating a corrected QTcF of >450 msec or other concerning arrhythmia. For participants not undergoing CHMI-T after booster vaccine, no EKG will be required
  • Current or planned use of medications known to significantly prolong the QT interval or otherwise interfere with study agents.

  • Smoking more than 5 cigarettes or equivalent per day and unable to stop smoking for the duration of admission. Participants may smoke up to 5 cigarettes or equivalent per day for the rest of the study (by attestation).

  • History of alcohol use disorder (exceptions may be made at the investigator s discretion if they have completed treatment or are otherwise currently abstinent) or refusal to agree to refrain from drinking from the day of the challenge agent inoculation until completion of their antimalarial course.

Co-enrollment guidelines: Co-enrollment in other trials is restricted. Consideration for coenrollment, other than enrollment on trials evaluating the use of an investigational malaria vaccine as described above will require the approval of the principal investigator. Study staff should be notified of co-enrollment on any other protocol.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Booster Vaccine

A fourth (booster) dose of of Pvs230D1-EPA/MM will be given to participants who previously received the primary vaccine series while enrolled in NIH protocol 001501, at a dose identical to that which the participant received under NIH Protocol 1501 (i.e., 5microg Pvs230D1-EPA/50microg MM, 25microg Pvs230D1-EPA/50microg MM, or 50microg Pvs230D1-EPA/50microg MM).Optionally, two to twelve weeks after the final vaccination, challenge agent derived from a cell bank of cryopreserved blood-stage P. vivax (PvHMB-CCE001) will be administered intravenously (IV). Participants will be monitored and admitted to the NIHCC to undergo safety monitoring, transmission assays, and receive antimalarial treatment.

Challenge agent derived from cryopreserved cell bank PvHMB-CCE001 which contains the P. vivax isolate HMP013 in red blood cells derived from a healthy US adult donor.

A protein subunit conjugate vaccine Pvs230D1-EPA formulated with adjuvant Matrix-M

Comparatore attivo: Open-label control

Participants enrolled on NIH protocol 001970, Induced blood-stage malaria in healthy malaria-naive adults to assess the safety and infectivity of Plasmodium vivax challenge agent and evaluate transmission in mosquito feeding assays , will serve as open-label controls.

Challenge agent derived from cryopreserved cell bank PvHMB-CCE001 which contains the P. vivax isolate HMP013 in red blood cells derived from a healthy US adult donor.

Sperimentale: Primary Vaccine Series

Three doses of 5microg Pvs230D1-EPA/50microg MM will be administered at 1-month intervals, via intramuscular (IM) injection. Two to twelve weeks after the final vaccination, challenge agent derived from a cell bank of cryopreserved blood-stage P. vivax (PvHMB-CCE001) will be administered intravenously (IV). Participants will be monitored and admitted to the NIHCC to undergo safety monitoring, transmission assays, and receive antimalarial treatment.

Challenge agent derived from cryopreserved cell bank PvHMB-CCE001 which contains the P. vivax isolate HMP013 in red blood cells derived from a healthy US adult donor.

A protein subunit conjugate vaccine Pvs230D1-EPA formulated with adjuvant Matrix-M

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
To assess efficacy of Pvs230D1-EPA/MM vaccine using the CHMI-T model.
Lasso di tempo: Day 11 after the administration of the Pv challenge agent.

Transmission of P. vivax to Anopheles spp. using direct skin feeding (DSF) assay as determined by the detection and quantification of oocysts following midgut dissection.

Day 11 after the administration of the Pv challenge agent.
To assess the safety and reactogenicity of Pvs230D1-EPA/MM primary vaccine series in healthy malaria-naive adults.
Lasso di tempo: From inoculation (day 0) to end of study visit (day 224)

Incidence of immediate AEs within 30 minutes following each vaccine dose.Incidence and severity of local and systemic AEs within 14 days following each vaccine dose. Incidence of SAEs for the entire study duration.

From inoculation (day 0) to end of study visit (day 224)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
To determine the antibody response to Pvs230D1-EPA/MM primary series and booster vaccine.
Lasso di tempo: From inoculation (day 0) to end of study visit (day 224)

Anti-Pvs230D1 antibody levels and durability of immune response, as measured by enzyme-linked immunosorbent assay (ELISA), at various time points.

From inoculation (day 0) to end of study visit (day 224)
To assess functional activity of Pvs230D1-EPA/MM primary vaccine series and booster vaccine using the CHMI-T model.
Lasso di tempo: From inoculation (day 0) to end of study visit (day 224).

Transmission of P. vivax to Anopheles spp. using membrane feeding assays (MFA) as determined by the detection and quantification of oocysts following midgut dissection and/or other methods.

From inoculation (day 0) to end of study visit (day 224).
To assess the safety of CHMI-T.
Lasso di tempo: From day of Pv challenge agent administration (C0) until 34 days post inoculation.

Incidence and severity of CHMI-T-related local and systemic AEs or SAEs from challenge administration and through mosquito procedures, until 34 days post-challenge agent inoculation.

From day of Pv challenge agent administration (C0) until 34 days post inoculation.
To assess the safety and reactogenicity of Pvs230D1-EPA/MM booster vaccine in healthy malaria-naive adults.
Lasso di tempo: From inoculation (day 0) to end of study visit (day 224).

Incidence of immediate adverse events (AEs) within 30 minutes following booster vaccine. Incidence and severity of local and systemic AEs within 14 days following booster vaccine. Incidence of SAEs following booster vaccine for the entire study duration.

From inoculation (day 0) to end of study visit (day 224).

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Shanan R Immel, M.D., National Institute of Allergy and Infectious Diseases (NIAID)

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

17 novembre 2026

Completamento primario (Stimato)

1 novembre 2029

Completamento dello studio (Stimato)

1 novembre 2029

Date di iscrizione allo studio

Primo inviato

7 novembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

11 novembre 2026

Primo Inserito (Effettivo)

12 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

11 novembre 2026

Ultimo verificato

3 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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