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Performance Evaluation of Mpox Molecular POC Diagnostics

Clinical Performance Evaluation of Novel Rapid Molecular Point-of-care (POC) Diagnostics for Mpox Virus

PP016 is a FIND-sponsored retrospective clinical performance study evaluating rapid molecular point-of-care (mPOC) tests for the detection of Mpox virus (MPXV) using archived lesion swab specimens collected in Uganda. Conducted at the Central Public Health Laboratory (CPHL) in Kampala, the study compares up to three investigational assays-Genes2Me VZV-Q, KH Medical RADI-ONE Mpox, and SD Biosensor STANDARD M10 MPX/OPX-against the BioPerfectus laboratory PCR reference test. The primary objective is to determine the sensitivity and specificity of each assay for detecting MPXV in archived positive and negative samples, while secondary analyses assess performance by Ct value and viral clade. The study uses a blinded, non-interventional case-control design with de-identified specimens collected since 2020. Approximately 80 samples per device evaluation are included. PP016 was initiated in response to ongoing mpox outbreaks and the need for accurate decentralized diagnostics in low-resource settings. The study complies with ISO 20916, ICH-GCP principles where applicable, and Ugandan ethical and regulatory requirements, with findings expected to support future regulatory approvals and implementation of rapid mpox diagnostics in low- and middle-income countries

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Szczegółowy opis

PP016 is a FIND-sponsored retrospective, non-interventional clinical performance evaluation study designed to assess the diagnostic accuracy and operational suitability of up to three rapid molecular point-of-care (mPOC) tests for the detection of Mpox virus (MPXV) using archived lesion swab specimens collected in Uganda. The study, titled "Clinical Performance Evaluation of Novel Rapid Molecular Point-of-Care Diagnostics for Mpox Virus," is being conducted at the Central Public Health Laboratory (CPHL) in Kampala, Uganda. The study was developed in response to the growing public health importance of mpox, particularly following the 2022 and 2024 WHO Public Health Emergencies of International Concern (PHEICs), and the ongoing outbreaks affecting several African countries including Uganda, where thousands of confirmed cases have been reported. Because conventional laboratory PCR testing remains centralized and difficult to access in many low-resource or decentralized settings, the study aims to determine whether rapid molecular POC assays can provide accurate and scalable diagnostic alternatives to improve outbreak response, surveillance, patient management, and contact tracing. The study evaluates three investigational molecular diagnostic platforms: the VZV-Q Real-Time PCR Kit for OnePCR (Genes2Me, India), the RADI-ONE Mpox Detection Kit (KH Medical, South Korea), and the STANDARD M10 MPX/OPX assay (SD Biosensor, South Korea). Their performance is compared against the laboratory-based BioPerfectus Monkeypox Virus Real Time PCR Kit, which serves as the reference standard and is currently listed under the African Medicines Regulatory Harmonisation Emergency Use Listing for mpox diagnosis. The study uses archived lesion swab samples stored in viral or universal transport medium from suspected mpox cases collected since 2020 under routine surveillance or prior research activities. Eligible samples must have known PCR status, adequate volume for both reference and index testing, and acceptable storage conditions.

The primary objective is to determine the clinical sensitivity/positive percent agreement (PPA) and specificity/negative percent agreement (NPA) of each investigational assay relative to the reference PCR, while secondary objectives include assessing performance according to PCR cycle threshold (Ct) values as a proxy for viral load and evaluating potential differences in performance by circulating mpox virus clades if such information is available. Statistical analyses will use Wilson score confidence intervals, with subgroup analyses by age, sex, Ct value, and viral clade. The study follows a blinded case-control design in which specimens are de-identified, shuffled, relabeled with unique FIND study identifiers, and tested independently to minimize bias. Reference PCR testing is performed first to confirm specimen quality and classification before testing on the investigational devices. Invalid or inconclusive results are repeated once and documented according to predefined procedures. No patient recruitment or intervention occurs, and test results are not used for clinical management, making the study low risk from an ethical and safety perspective.

Data are collected using OpenClinica Enterprise Edition, a validated electronic data capture system with audit trails and secure cloud hosting. FIND oversees monitoring, quality assurance, operator training, and regulatory compliance throughout the study.

The study is funded by FIND with support from the Government of the Netherlands and is expected to generate independent evidence to support regulatory submissions, procurement decisions, WHO evaluation processes, and future implementation of rapid mpox diagnostics in low- and middle-income countries.

Typ studiów

Obserwacyjny

Zapisy (Szacowany)

80

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko
  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie dotyczy

Metoda próbkowania

Próbka prawdopodobieństwa

Badana populacja

The study population consists of archived skin lesion swabs specimens. These were previously collected from individuals suspected of mpox infection - confirmed by PCR as MPXV positive or negative - under research studies and/or public health surveillance protocols during past and ongoing mpox outbreaks and available in the selected clinical sites.

Opis

Inclusion Criteria:

  • Lesion swabs stored in VTM/UTM (non-inactivating)
  • Aliquot with sufficient volume to run the reference PCR and at least one index test (≥2600 μL per pair reference-index tests: ideally at least 1400 μL for 3 index tests and 1200 μL for reference PCR, including 1 possible repeat per test)
  • Available PCR result for specimen selection (i.e. confirmed MPXV positive or negative)
  • Samples collected from 2020 onwards.

Exclusion Criteria:

  • Unknown date of collection
  • >3 freeze-thaw cycles of sample.
  • Samples collected with expired swab collection devices or UTM/VTM

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
Interwencja / Leczenie
Positive samples
50 confirmed MPXV-positive samples
Each (negative and positive) sample will be tested on the standard of reference and the investigational IVD
Negative samples
30 confirmed MPXV-negative samples
Each (negative and positive) sample will be tested on the standard of reference and the investigational IVD

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Point estimates of sensitivity, specificity, positive and negative predictive value (PPV and NPV respectively) with 95% confidence intervals.
Ramy czasowe: July-August 2026
Point estimates of sensitivity, specificity, positive and negative predictive value (PPV and NPV respectively) with 95% confidence intervals.
July-August 2026

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Point estimates of sensitivity/PPA stratified by Ct values of the reference PCR test.
Ramy czasowe: July-August 2026
Point estimates of sensitivity/PPA stratified by Ct values of the reference PCR test.
July-August 2026
Point estimates of sensitivity/PPA and specificity/NPA with 95% confidence intervals stratified by virus clade.
Ramy czasowe: July-August 2026
Point estimates of sensitivity/PPA and specificity/NPA with 95% confidence intervals stratified by virus clade.
July-August 2026

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

15 czerwca 2026

Zakończenie podstawowe (Szacowany)

15 sierpnia 2026

Ukończenie studiów (Szacowany)

15 września 2026

Daty rejestracji na studia

Pierwszy przesłany

27 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

27 maja 2026

Pierwszy wysłany (Rzeczywisty)

2 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

2 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

27 maja 2026

Ostatnia weryfikacja

1 maja 2026

Więcej informacji

Terminy związane z tym badaniem

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Małpa ospa

Badania kliniczne na MPOX IVD test

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