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Clinical trial intelligence report
Establishment a Nucleic Acid Rapid Detection Technology Platform for Detecting Pathogenic Bordetella and Its Drug Resistance Genes
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 13, 2026
NCT ID
NCT04535505
Status
WITHDRAWN
Phase
Withdrawn
Sponsor
Children's Hospital of Fudan University
Executive brief
Investment-Ready Snapshot
The proposed CPA platform utilizing CRISPR technology aims to provide a rapid and accurate diagnostic tool for detecting Bordetella species and their associated drug resistance genes. Given the ongoing global concerns regarding pertussis outbreaks, this technology could address a significant unmet need in infectious disease diagnostics. However, the trial has been withdrawn, indicating potential challenges in development or execution. The competitive landscape includes existing diagnostic methods such as culture and PCR, which may limit market entry unless the new platform demonstrates superior accuracy and speed. Diligence is required to assess the reasons for withdrawal and any implications for future development or partnerships.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04535505
Indication
Pertussis
Modality
small molecule
Target
Pathogenic Bordetella species and their drug resistance genes, specifically targeting Bordetella pertussis and its erythromycin resistance mechanisms.
Intervention
Detection pathogenic pertussis by cross primer constant temperature amplification (CPA) and drug resistant genes of erythromycin by CRISPR technology
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.