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.
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.
2 sites in 2 countries
China1 site, 1 recruiting
- Recruiting
Women's Hospital School Of Medicine Zhejiang University
Hangzhou, Zhejiang, 310006
Jinglan Zhang, PhD, +86 571 82295074, jinglanzhang@foxmail.com
Hong Kong1 site, 1 recruiting
- Recruiting
The Chinese University of Hong Kong
Hong Kong
Kwong Wai Choy, PhD, (852) 3505 2807, richardchoy@cuhk.edu.hk
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.
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)
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.
- First posted6 Aug 2025
- Study start16 Sep 2025
- Primary completion31 Dec 2027 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Genetic DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Women's Hospital School Of Medicine Zhejiang University
- Sponsor type
- University, hospital or other
- Collaborators
- University of Pennsylvania, Chinese University of Hong Kong
- Responsible party
- Sponsor
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.
Study at a glance
From the registry record, last updated by the sponsor on 17 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prenatal Cell-free DNA Screening in Pregnancies With Diverse Genetic Risk Profiles Utilizing Targeted and Whole-exome Sequencing
- ClinicalTrials.gov ID
- NCT07106853
- Acronym / sponsor ID
- IRB-20250133-R
- Conditions
- Genetic Disease
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 1,600 participants (estimated)
- Lead sponsor
- Women's Hospital School Of Medicine Zhejiang UniversityUniversity, hospital or other
- Collaborators
- University of Pennsylvania, Chinese University of Hong Kong
- Study start
- 16 Sep 2025 (actual)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 31 Dec 2027 (estimated)
- First posted
- 6 Aug 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Age groups
- 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
Key inclusion criteria (8 listed)
- 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:
- 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
Key exclusion criteria (4 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
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
1 secondary outcome
Assess efficacy across diverse genetic risk populations by analyzing detection rates of pathogenic variants associated with fetal indications.
Time frame: 8 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Sep 2026.
- Individual participant dataSharing planned: Yes. IPD will be part of the data published for the study results.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 2 countries: see every site and its status.
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.