- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07558122
Malaria CVD 36000; Gates INV090205
Phase I, Double-blind, Randomized Study of Physiological Parameters Biosensor Detection Device(s) Diagnosis of P. Falciparum NF54 Strain Malaria Following Controlled Human Malaria Infection and Post-hoc Analysis of Wearable Biosensor Device Detection
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Kirsten Lyke, MD
- Numéro de téléphone: 410-706-6156
- E-mail: klyke@som.umaryland.edu
Lieux d'étude
-
-
Maryland
-
Baltimore, Maryland, États-Unis, 21201
- University of Maryland, Baltimore, Center for Vaccine Development and Global Health
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
La description
Inclusion Criteria:
- Male or non-pregnant, non-breastfeeding female between 18 and 50 years of age (inclusive) at the time of consent.
- Participants must be able to provide written informed consent.
- Participants must be healthy as established by medical history and clinical examination at study entry.
- Participants must pass a comprehension (defined as 80%) test and be able to comply with all study requirements.
- Both males and females are eligible to participate as per the following:
Participants physically capable of pregnancy must agree to use effective contraception to avoid pregnancy from 28 days before enrollment through 10 months after last administration of investigational product are eligible to participate. An effective contraceptive method is defined as one that results in a failure rate of less than 1% per year when it is used consistently and correctly. Adequate contraceptive precautions include intrauterine contraceptive device, oral contraceptives, diaphragm, or condom in combination with contraceptive jelly, cream, or foam; Norplant® or Depo-Provera®, through the completion of study visits to minimize any potential risk.
i. Effective contraception does not apply to participants of child-bearing potential with same sex partners, when this is their preferred and usual lifestyle.
ii. Adequate contraception does not apply to women with documented surgical sterility (tubal ligation, bilateral oophorectomy, salpingectomy, or hysterectomy), congenital sterility, who have a diagnosis of infertility and are not undergoing treatment, or women who have not had a menstrual period in at least 1 year
Exclusion Criteria:
- Women who are pregnant or breastfeeding
- Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination (no laboratory testing required)
- History of malaria infection, or history > 6 months spent in a malaria endemic region within 5 years prior to enrollment.
Participant seropositive for hepatitis B surface antigen (HBsAg), hepatitis C virus antibodies (anti-HCV), or human immunodeficiency virus antibodies (anti-HIV).
Note: Prior participants of HIV vaccine studies may result in a false positive HIV antibody test, as such, in this scenario, participant will be eligible if they have a negative HIV RNA PCR at screening.
Safety laboratory test results within range at screening (as per FDA Toxicity Grading Scale, see Appendix A):
- White Blood Cell (WBC) 3,500-12,000/mm3
- WBC differential either within institutional normal range or accompanied by the PI or designee approval
- Platelets = 125,000 - 500,000/mm3
- Hemoglobin within institutional normal range or accompanied by the PI or designee approval
- Creatinine ≤ 1.1 x upper limit of normal (ULN)
- ALT ≤1.25 x ULN
- Grade 1 subclinical abnormalities in other chemistries will not lead to exclusion if the investigator considers them not clinically significant
- A 5-year cardiovascular risk of >10% using the Gaziano nomogram (Appendix B)
- Significant screening physical examination abnormalities at the discretion of the investigator, including a BMI > 35 kg/m2
- Electrocardiogram (ECG) with clinically significant abnormalities (examples may include: pathologic Q waves, significant ST-T wave changes, left ventricular hypertrophy, any non-sinus rhythm excluding isolated premature atrial contractions, right or left bundle branch block, advanced A-V heart block). ECG abnormalities determined by an investigator to be clinically insignificant as related to trial participation do not preclude trial enrollment. Consultation may be sought by a cardiologist at investigator discretion.
- Known intolerance to atovaquone or proguanil, and either artemether/lumefantrine or chloroquine phosphate
- Routine use of antibiotics, or use of antibiotics with known antimalarial effect (azithromycin, trimethoprim/sulfamethoxazole or tetracyclines) within 4 weeks prior to CHMI.
- Anticipated use of medications known to cause drug reactions with chloroquine or atovaquone-proguanil (Malarone®) such as cimetidine, metoclopramide, antacids, and kaolin.
- Administration of immunoglobulins and/or any blood products during the period starting 90 days preceding the CHMI or planned administration during the study period
- Planned administration or administration of a live vaccine/product not planned in the study protocol during the period starting 30 days prior to the CHMI until the study completion (routine vaccinations will be allowed if it is not administered within 14 days preceding or 21 days following CHMI)
- Use of any investigational or non-registered product (drug or vaccine during the period starting 30 days preceding the CHMI and/or planned use during the study period
- Chronic administration (defined as more than 14 days in total) of immunosuppressants or other immune-modifying drugs during the period starting 90days prior to the CHMI (for corticosteroids, this will mean prednisone >5mg/day or equivalent; inhaled, intranasal and topical steroids are allowed)
- 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 product (pharmaceutical product or device)
- Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions) or significant bruising or blood draws
- History of a splenectomy, sickle cell disease or sickle cell trait
- History of skeeter syndrome or anaphylactic response to mosquito-bites
- Autoimmune disease or history of autoimmune disease
- History of any reaction or hypersensitivity likely to be exacerbated by any component of the study product or related to a study procedure
- Major congenital defects or serious chronic illness
- Presence of any implanted device which could bias biosensor data (e.g., pacemaker, etc.)
- Acute disease and/or fever (≥37.5°C/99.5°F oral body temperature) at the time of enrollment: note that a participant with a minor illness such as mild diarrhea, mild upper respiratory infection, etc., without fever, may be enrolled at the discretion of the investigator
- Acute or chronic, clinically significant pulmonary, cardiovascular, hepatic, neurological disorders, seizures or renal functional abnormality, as determined by history, physical examination or laboratory screening tests
- History of bipolar disorder, schizophrenia, hospitalization in the past year for a mental health disorder, or any other psychiatric condition, which in the opinion of the investigator prevents the participant from participating in the study
- Any current medical, psychiatric, occupational, or substance abuse problems that, in the opinion of the Investigator, will make it unlikely that the participant will comply with the protocol.
- Any other condition which, in the opinion of the investigator, prevents the participant from participating in the study
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Diagnostique
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: PfSPZ Challenge
0.5 mL single-dose of PfSPZ Challenge (strain NF54)
|
PfSPZ Challenge (NF54) administered as a single dose by direct venous inoculation (DVI)
Investigational, wearable biosensing devices.
The objective would be to collect biosensor data for correlation to known malaria infection by reference diagnostic testing and with physiological (clinical) data.
|
|
Comparateur placebo: Placebo
Normale saline placebo
|
Placebo salin normal
Investigational, wearable biosensing devices.
The objective would be to collect biosensor data for correlation to known malaria infection by reference diagnostic testing and with physiological (clinical) data.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Presence of detectable malaria parasitemia following controlled human malaria infection exposure by the Direct Venous Inoculation (DVI) of cryopreserved P. falciparum NF54-strain sporozoites
Délai: From challenge to the end of participation at day 56
|
Presence or absence of RT-qPCR through Day 28 (unit - Ct value)
|
From challenge to the end of participation at day 56
|
|
Presence of detectable malaria parasitemia following controlled human malaria infection exposure by the Direct Venous Inoculation (DVI) of cryopreserved P. falciparum NF54-strain sporozoites
Délai: From challenge to the end of participation at day 56
|
Presence of absence of Thick Blood Smear - unit - parasite/mm3 or mL
|
From challenge to the end of participation at day 56
|
|
Time of detectable malaria parasitemia following controlled human malaria infection exposure by the Direct Venous Inoculation (DVI) of cryopreserved P. falciparum NF54-strain sporozoites
Délai: From challenge to the end of participation at day 56
|
Time to Pf infection (unit - days)
|
From challenge to the end of participation at day 56
|
|
Presence or absence of temperature associated with pre-infection, asymptomatic parasitemia and symptomatic parasitemia
Délai: From challenge to the end of participation at day 56
|
From challenge to the end of participation at day 56
|
|
|
Presence or absence of heart Rate changes associated with pre-infection, asymptomatic parasitemia and symptomatic parasitemia
Délai: From challenge to the end of participation at day 56
|
From challenge to the end of participation at day 56
|
|
|
Presence or absence of Respiratory Rate associated with pre-infection, asymptomatic parasitemia and symptomatic parasitemia
Délai: From challenge to the end of participation at day 56
|
From challenge to the end of participation at day 56
|
|
|
Presence or absence of Solicited Systemic Symptoms associated with pre-infection, asymptomatic parasitemia and symptomatic parasitemia
Délai: From challenge to the end of participation at day 56
|
(yes/no to headache, fatigue/malaise, myalgia, arthralgia, nausea, abdominal pain, vomiting)
|
From challenge to the end of participation at day 56
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- HP-00118316
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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 .