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AzTrials

Genetic DiseaseNCT07106853

Prenatal Cell-free DNA Screening in Pregnancies With Diverse Genetic Risk Profiles Utilizing Targeted and Whole-exome Sequencing

An observational study of Genetic Disease, run by Women's Hospital School Of Medicine Zhejiang University at 2 sites in 2 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This multicenter study aims to recruit a minimum of 1,600 pregnant women, encompassing individuals with varying levels of genetic risk. The study particularly focuses on cases with increased fetal nuchal translucency (NT ≥3.5 mm), additional ultrasound markers, and/or fetal structural anomalies. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Genetic Disease
How many people
1,600 participants
Where
2 sitesin 2 countries
Study dates
16 Sep 2025to 31 Dec 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Adult, Older adult

Study population: * Adult pregnant woman (≥18 years old) * Gestational age between 9+0 and 25+6 weeks * Singleton pregnancy * Pregnancy with indications for prenatal diagnosis due to: * Increased nuchal translucency (NT) ≥3.5 mm: capped at 25% of total subjects * Increased NT ≥3.5 mm AND presence of any other "soft marker" or structural anomaly: capped at 25% of total subjects * Presence of structural anomaly: at least 50% of total subjects * Agree to participate in the clinical study for being followed-up and accept at least one molecular diagnosis (diagnostic procedures performed on prenatal invasive specimens, product of conception, umbilical cord blood, or other specimens) and possible family member testing

Who may be able to join

  • Adult pregnant woman (≥18 years old)
  • Gestational age between 9+0 and 25+6 weeks
  • Singleton pregnancy
  • Pregnancy with indications for prenatal diagnosis due to:
  • Increased nuchal translucency (NT) ≥3.5 mm: capped at 25% of total subjects
  • Increased NT ≥3.5 mm AND presence of any other "soft marker" or structural anomaly: capped at 25% of total subjects
  • Presence of structural anomaly: at least 50% of total subjects
  • Agree to participate in the clinical study for being followed-up and accept at least one molecular diagnosis (diagnostic procedures performed on prenatal invasive specimens, product of conception, umbilical cord blood, or other specimens) and possible family member testing

Who cannot join

  • Age under 18 years
  • Gestational age is less than 9+0 weeks or greater than 25+6 weeks
  • One parent or other family member has a known pathogenic variant linked to the fetal ultrasound finding(s)
  • Conditions affecting the accuracy of cfDNA assay (e.g., maternal malignancy during pregnancy, maternal allogeneic blood transfusion, organ transplantation, or cell therapy within the past year)

Trial locations and contacts

2 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

Jinglan Zhang, PhD contact

86-18057173728

jinglanzhang@foxmail.com

2 sites in 2 countries

China1 site, 1 recruiting
  • Women's Hospital School Of Medicine Zhejiang University

    Hangzhou, Zhejiang, 310006

    Jinglan Zhang, PhD, +86 571 82295074, jinglanzhang@foxmail.com

    Recruiting

Other trials in China

Hong Kong1 site, 1 recruiting
  • The Chinese University of Hong Kong

    Hong Kong

    Kwong Wai Choy, PhD, (852) 3505 2807, richardchoy@cuhk.edu.hk

    Recruiting

Other trials in Hong Kong

About this study

This multicenter study aims to recruit a minimum of 1,600 pregnant women, encompassing individuals with varying levels of genetic risk. The study particularly focuses on cases with increased fetal nuchal translucency (NT ≥3.5 mm), additional ultrasound markers, and/or fetal structural anomalies. Peripheral blood samples of eligible participants will be collected for two state-of-the-art cfDNA tests based on coordinative allele-aware target enrichment sequencing (COATE-seq): (1) a targeted panel to screen for frequent chromosomal aneuploidies, microdeletions/duplications, and dominant single-gene conditions, and (2) comprehensive whole-exome cfDNA sequencing for aneuploidies, microdeletions/duplications, monogenic variants (both dominant and recessive variants), uniparental disomy, and hydatidiform moles. The results of both cfDNA tests will be compared with those from invasive or postnatal diagnostic testing. Pregnancy outcome will be followed up to six weeks postpartum. The primary goal is to determine the clinical validity of targeted and whole exome cfDNA analyses, assessed through sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) relative to diagnostic standards. Secondary goal is to assess efficacy across diverse genetic risk populations by analyzing detection rates of pathogenic variants associated with fetal indications. The clinical utility of cfDNA screening will also be evaluated by its impact on clinical management decisions, including follow-up diagnostic procedures or prenatal/perinatal interventions.

Read the detailed description

This is a prospective, multicenter clinical study evaluating the clinical validity and utility of a next-generation non-invasive prenatal screening platform, COATE-seq (Coordinative Allele-Aware Target Enrichment Sequencing). COATE-seq is a cfDNA-based approach that integrates hybrid capture panel sequencing with whole-exome sequencing (WES) from a single maternal plasma sample, enabling detection of a broad spectrum of fetal genetic conditions. These include common and rare aneuploidies, clinically significant microdeletions, monogenic pathogenic variants, uniparental disomy (UPD), and molar pregnancies.

The platform leverages coordinated allelic modeling and deep sequencing to enhance sensitivity for low-allelic-fraction variants, including those in autosomal recessive and dominant genes. The panel-based component targets 56 monogenic conditions selected using the SEPH framework (Severe, Early-onset, Prevalent, High detectability), while the WES component interrogates approximately 19,000 protein-coding genes to enable secondary and exploratory analyses of ultra-rare or novel variants. Variant interpretation adheres to ACMG/AMP guidelines, and only pathogenic or likely pathogenic variants associated with severe outcomes are reported.

The study is designed to benchmark the performance of this integrated assay against conventional diagnostic standards, including karyotyping, chromosomal microarray (CMA), targeted gene sequencing, whole-exome sequencing, and whole-genome sequencing. Reference testing is performed prenatally or postnatally, and in select cases, UPD is confirmed via methylation-specific PCR or short tandem repeat (STR) analysis.

Data collected across the study include:

Clinical history and prenatal imaging findings

cfDNA sequencing results from both targeted panels and exome-based assays

Confirmatory diagnostic results

Pregnancy outcomes and postnatal phenotypes, where available

Performance metrics including sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) will be calculated in subjects with complete cfDNA and diagnostic data. Additional analyses will assess detection rates stratified by clinical indication (such as abnormal ultrasound findings), quantify the incremental yield of WES compared to panel-only testing, and evaluate the downstream clinical impact on decision-making and pregnancy management.

COATE-seq incorporates a rigorously validated bioinformatics pipeline for fetal fraction estimation, detection of allelic imbalance, chromosomal dosage, copy number variation (CNV) analysis, and pathogenic variant annotation. Quality assurance procedures are applied throughout sample processing, sequencing, and data interpretation, including safeguards during plasma handling, DNA extraction, target capture, library construction, and analytical review.

The study complies with Good Clinical Practice (GCP) and relevant regulatory and ethical guidelines. Institutional Review Board (IRB) approval is obtained at all participating sites, and informed consent is secured prior to enrollment. The results of this study will inform best practices for expanded cfDNA screening in prenatal care and contribute to the evidence base supporting the clinical integration of comprehensive molecular testing for fetal genetic conditions. Scientific findings will be disseminated through peer-reviewed publications and conference presentations.

Conditions
Genetic Disease
Medical subject headings
Genetic Diseases, Inborn

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Determine the clinical validity of targeted and whole exome cfDNA analyses, assessed through sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) relative to diagnostic standards.

    Measured: 18 months

Secondary outcomes (1)
  1. Assess efficacy across diverse genetic risk populations by analyzing detection rates of pathogenic variants associated with fetal indications.

    Measured: 8 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Aug 2025
  2. Study start16 Sep 2025
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07106853
Sponsor's protocol ID
IRB-20250133-R
Status last verified
Sep 2026
First submitted
11 Jun 2025
Last updated
17 Sep 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: IPD will be part of the data published for the study results.

Questions about this trial

What is this clinical trial studying?

An observational study of Genetic Disease, run by Women's Hospital School Of Medicine Zhejiang University at 2 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 17 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in China, Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Jinglan Zhang, PhD (86-18057173728, jinglanzhang@foxmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Determine the clinical validity of targeted and whole exome cfDNA analyses, assessed through sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) relative to diagnostic standards. (time frame: 18 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Sep 2026.

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