TrialSignal
Clinical trial intelligence report
An Open-Label, Two-Arm, Non-Randomized Clinical Study On The Safety And Efficacy Of Instantaneous CRISPR/Cas9 Gene Editing Therapy For Treating Chinese Patients With HPV-16-Related High-Grade Squamous Intraepithelial Lesions (HSIL)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT07170254-Jul 28, 2026
NCT ID
NCT07170254
Status
RECRUITING
Phase
Not Applicable (NA)
Sponsor
Shanghai BDgene Co., Ltd.
Executive brief
Investment-Ready Snapshot
Shanghai BDgene Co., Ltd. is advancing a novel CRISPR/Cas9 gene editing therapy (BD114) for the treatment of HPV-16-related high-grade squamous intraepithelial lesions (HSIL). The study is currently recruiting participants in Shanghai, China, with an estimated completion date in December 2026. The market for cervical cancer prevention and treatment is significant, particularly in regions with high HPV prevalence. If successful, BD114 could position BDgene as a leader in gene therapy for HPV-related conditions, although it will face competition from existing treatments and emerging therapies. Diligence should focus on regulatory pathways, potential market entry barriers, and the evolving landscape of gene editing technologies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07170254
Indication
High-grade Squamous Intraepithelial Lesions (HSIL)
Modality
gene therapy
Target
CRISPR/Cas9 gene editing targeting HPV-16 E6/E7 genes.
Intervention
BD114VLP, or BD114, BD114VLP or BD114 plus Gel
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.