Performance Evaluation of Mpox Molecular POC Diagnostics
Clinical Performance Evaluation of Novel Rapid Molecular Point-of-care (POC) Diagnostics for Mpox Virus
調査の概要
詳細な説明
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.
研究の種類
入学 (推定)
参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
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
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Point estimates of sensitivity, specificity, positive and negative predictive value (PPV and NPV respectively) with 95% confidence intervals.
時間枠:July-August 2026
|
Point estimates of sensitivity, specificity, positive and negative predictive value (PPV and NPV respectively) with 95% confidence intervals.
|
July-August 2026
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Point estimates of sensitivity/PPA stratified by Ct values of the reference PCR test.
時間枠: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.
時間枠:July-August 2026
|
Point estimates of sensitivity/PPA and specificity/NPA with 95% confidence intervals stratified by virus clade.
|
July-August 2026
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- PP016
医薬品およびデバイス情報、研究文書
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
サル痘の臨床試験
-
Children's Hospital of Fudan UniversityPeople's Hospital of Xinjiang Uygur Autonomous Region; Hainan women and children medical center と他の協力者完了さまざまな高度での健康な新生児の POX 範囲 | 新生児における主要なCHDをスクリーニングするためのPOX閾値中国
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