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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.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Geschätzt)

220

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Maryland
      • Bethesda, Maryland, Vereinigte Staaten, 20892
        • National Institutes of Health Clinical Center
        • Kontakt:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • Telefonnummer: TTY dial 711 (800) 411-1222
          • E-Mail: ccopr@nih.gov
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 54 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

  • 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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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

Aktiver Komparator: 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.

Experimental: 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

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
To assess efficacy of Pvs230D1-EPA/MM vaccine using the CHMI-T model.
Zeitfenster: 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.
Zeitfenster: 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)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
To determine the antibody response to Pvs230D1-EPA/MM primary series and booster vaccine.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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).

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Ermittler

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

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

18. November 2026

Primärer Abschluss (Geschätzt)

1. November 2029

Studienabschluss (Geschätzt)

1. November 2029

Studienanmeldedaten

Zuerst eingereicht

7. November 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. November 2026

Zuerst gepostet (Tatsächlich)

12. November 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

13. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

12. November 2026

Zuletzt verifiziert

3. November 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • 10002627
  • 002627-I

Plan für individuelle Teilnehmerdaten (IPD)

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UNENTSCHIEDEN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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