Newborn Screening Programmes for Rare DiseasesPGC1NCT06875089
A Pilot Study to Assess the Feasibility and Acceptability of Newborn Screening Using in Silico Panel-based Solo Genome Sequencing in France
An observational study of Newborn Screening Programmes for Rare Diseases, run by Centre Hospitalier Universitaire Dijon at 5 sites in France.
Trial summary
Newborn Screening (NBS) based on genome sequencing (GS) is currently the subject of particular attention at both European and international levels. Over the past three years, several publications have discussed the opportunities and challenges of using GS for NBS. Read more about this study
- Who is it for?
- Ages 0 to 28 days
- Conditions the study is for
- Newborn Screening Programmes for Rare Diseases
- What is being tested?
- pGS-NBS, Satisfaction questionnaire and interview with HSS researcher
- How many people
- 5,000 participants
- Where
- 5 sitesFrance
- Study dates
- 5 May 2025to Jul 2032
- 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 0 to 28 days
- All sexes
- Child
Study population: all the parents of live newborns in each participating maternity unit
Who may be able to join
- For satisfaction study about the information \& identification of determinants of acceptability :
- All future parents approached for whom the unborn child will be cared for in the participating maternity unit
- At least one parent/legal guardian who received information about the study
- Future parents/legal guardian who do not object to the use of their data
- Parent(s) or legal guardian(s) affiliated to a social security system or beneficiaries of such a system
- For pGS-NBS :
Show all 14Show fewer
- All babies born in one of the participating centers or born by chance outside the maternity but whom care will be carried out in the participating center
- Newborn who are less than 28 days at the date of the collection of PGC1 blotting paper
- At least one biological parent who received information about the study
- Parent(s) or legal guardian(s) who do not object to "conventional" NBS
- At least one parent/legal guardian able to provide consent for testing the infant
- Informed consent signed by at least one parent/legal guardian
- Agreement of the second parent/legal guardian for testing the infant (unless he is unknown or loss of contact) obtained from the first parent/legal guardian if his written informed consent has not been obtained
- Parent(s) or legal guardian(s) affiliated to a social security system or beneficiaries of such a system
Who cannot join
- Non inclusion criteria for satisfaction studies and pGS-NBS :
- Non-inclusion criteria for parents/legal guardians :
- Parent(s) or legal guardian(s) under legal protection (guardianship, tutorship) or to a court order Non-inclusion criteria for newborn
- Babies born under anonymous birth according to the French law, known as "nés sous X"
Trial locations and contacts
5 sites in 1 country. Contact the study team or a site near you to ask about taking part.
5 sites in 1 country
France5 sites, 5 recruiting
- Not yet recruiting
CHU d'Angers
Angers, 49933
Estelle COLIN, 0241353470 ext. +33, escolin@chu-angers.fr
- Not yet recruiting
CHU Besançon
Besançon, 25000
Nicolas MOTTET, 0381218505 ext. +33, N1mottet@chubesancon.fr
- Recruiting
CHU Dijon Bourgogne
Dijon, 21000
Laurence OLIVIER-FAIVRE, 0380295313 ext. +33, laurence.faivre@chu-dijon.fr
- Not yet recruiting
CHU Hôtel Dieu
Nantes, 44093
Sandra MERCIER, 0240083245 ext. +33, sandra.mercier@chu-nantes.fr
- Not yet recruiting
CHU Rennes - Hôpital Sud
Rennes, 35203
Laurent PASQUIER, 0299266744 ext. +33, laurent.pasquier@chu-rennes.fr
About this study
Official title: A Pilot Study to Assess the Feasibility and Acceptability of Newborn Screening Using in Silico Panel-based Solo Genome Sequencing in France PERIGENOMED-CLINICS 1 (PGC1 Study)
Newborn Screening (NBS) based on genome sequencing (GS) is currently the subject of particular attention at both European and international levels. Over the past three years, several publications have discussed the opportunities and challenges of using GS for NBS. To date, only two Chinese programs have published their results, the first on a series of 29,601 healthy newborns and the second on a series of 10,334 healthy newborns and 668 high-risk infants. Globally, more than twenty pilot projects are underway, although none has been initiated within the French context thus far. Across the different pilot projects, various study designs are used. Most have opted for a targeted GS-based analysis to screen for pediatric-onset diseases. Some projects focus solely on diseases for which effective drugs or interventions exist to prevent or reduce symptoms. In contrast, others offer parents the option to screen their newborns for diseases without current treatment options, but for which a treatment is underdevelopment, or with interest in early management, a choice exercised by most parents. Indeed, early diagnosis of these diseases can help to introduce treatments or interventions when they become available, to participate in research trials on new treatments and to receive early management and genetic counseling.
In France, the national NBS program has long been recognized worldwide for its organizational quality and comprehensiveness, although, until recently, it has one of the lowest numbers of diseases screened in Europe. As of mid-2024, the French NBS only includes 14 serious diseases. Recently, the French bioethics law has evolved to allow the use of genetic testing as a first-line procedure for NBS. At the same time, the development and efficiency of genomic techniques and the rapid increase in the number of treatable rare diseases (RDs) raise questions about the acceptability and relevance of these genomic methods for NBS and its possible extension. The extension of NBS to many RDs of early onset represents a real public health challenge as RDs, 80% of which are of genetic origin, account for 10% of deaths before the age of 5.
Read more
The FHU TRANSLAD has elaborated the PERIGENOMED Project, a large-scale project which aims to assess the relevance of pGS-NBS in France (analytical and clinical validity, clinical utility and psychosocial, ethical and organizational issues).
The pGS-NBS (also known as in silico panel-based GS, i.e. an analysis carried out entirely using informatic tools) consists of bioinformatics filtering steps that return only selected variants and/or rare variants from targeted genes issued from GS. So, even if the source data comes from the GS, it is possible to configure the pipeline to return only those variations known to be responsible for specific RDs.
the PERIGENOMED Project will be led in two steps. The first pilot step (PERIGENOMED-CLINICS 1 - PGC1 Study), presented in this protocol, aims to evaluate the feasibility and acceptability of pGS-NBS France. This pilot study plans to screen 2,500 newborns using pGS-NBS targeting two lists of genes (1 corresponding to genes variables responsible of treatable rare diseases, 2 including genes variation leading to actionable rare diseases). In both lists only RDs of early onset are considered. PGC1 study will be carried in 5 healthcare centers in France, with results expected to be returned to clinicians within less than 4 weeks. It will also provide an understanding of the optimal information and analytical pathways, and the possible organizational repercussions of pGS-NBS as well as a first insight about the validity of the pGS-NBS and about the clinical course of newborns screened positive and with a confirmed RD Two studies in humanities and social sciences (HSS) will also be linked to PGC1 Study. The first will focus on the reasons given by decliners and on the medical and socio-economic characteristics (at the individual and contextual level) of decliners versus participants. The second will assess the psychosocial impact of result disclosure on families of positive newborns, comparatively of negative ones.
These initial results will provide the first outcomes before the launch of a second larger phase PERIGENOMED-CLINICS 2 (PGC2 Study - 22,000 newborns), designed for studying the implementation of such pGS-NBS in routine on a regional level.
- Being tested
- pGS-NBS, Satisfaction questionnaire, interview with HSS researcher, Qualitative and quantitative longitudinal exploration, Medical follow up
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
pGS-NBSGenetic
Collection of a second DBS card if the parents accept the pGS-NBS for their newborn
Satisfaction questionnaireOther
questionnaire on information process of parents informed about pGS-NBS
interview with HSS researcherOther
interview with a member of the HSS team on reasons for declining /accepting pGS-NBS
satisfaction questionnaireOther
questionnaire on results delivery in parents having accepted the pGS-NBS
Qualitative and quantitative longitudinal explorationOther
validated anxiety and depression scales to assess the psychosocial impact and perceived utility for families whose child screened negative among which 30 families will be interviewed. Interviews and validated anxiety and depression scales will be suggested to all families receiving positive screening results
Medical follow upOther
follow-up of true positives and false negatives based on medical records (vital status, care pathways) until 5 years after results delivery
| Study group | Role | What they receive |
|---|---|---|
| No participants | future families not taking part in the pGS- NBS study Receives: Other: Satisfaction questionnaire; Other: interview with HSS researcher | |
| Participants | future families who take part the pGS-NBS Receives: Genetic: pGS-NBS; Other: Satisfaction questionnaire; Other: interview with HSS researcher; Other: Qualitative and quantitative longitudinal exploration; Other: Medical follow up |
What is being measured
The primary outcome is the main question the study is designed to answer.
parents who have accepted the pGS-NBS for their children for Treatable list
number of families taking part the pGS-NBS (Treatable list) among the families who were offered the pGS-NBS in the centers over the inclusion period. If this number is at least of 603/1251, we will be able to reject that the percentage of acceptance is below 45% versus the alternative that it is greater Conversely, if the number is equal or below 602/1251, we will reject the hypothesis that the acceptability is at least 50%.
Measured: until 2 days after birth with extension up to 28 days in case of hospitalization in intensive care
results concerning the Treatable list returned to clinicians within 4 weeks following the sample
number of families for which the pGS-NBS results concerning the Treatable list are delivered to clinicians in less than 4 weeks among those who consent to the pGS-NBS. If this number is at least 219/220, we will reject our null hypothesis (i.e. that the feasibility rate is less than or equal to 95% versus the alternative hypothesis that it is greater).
Measured: 4 weeks following the sample
Secondary outcomes (10)
parents who have accepted the pGS-NBS for their children for Actionable list
percentage of families taking part to the pGS-NBS based on the complementary list of genes (Actionable list) among the families who were offered the GS NBS in the centers over the inclusion period
Measured: until 2 days after birth
results concerning the Actionable list returned to clinicians within 4 weeks following the sample,
Results concerning the Actionable list returned to clinicians, 4 weeks following the sample organizational indicators constributing to the feasibility assessment of the pGS-NBS : duration of analytical processes, human resources, technical difficulties, screenings requiring a 2nd sample,
Measured: 4 weeks following the sample
Questionnaire for parents' satisfaction with the screening and reporting processes
(flash questionnaire for all parents and complementary questionnaire for parents who accept it)
Measured: up to 4 weeks
profiles of parents who take part or not to pGS-NBS
Interviews
Measured: at the baseline
quantitative exploration
anxiety and depression scales
Measured: At : 1,6,12,24,36,48 and 60 months after positive results delivery At : 1 and 12 months after negative results delivery
pGS-NBS performance
Children with negative results identified as false negative by reference centers and/or NDBRD (National Data Bank for Rare Diseases) before age 5
Measured: 5 years;
Clinical evoluation of newborns with true positive results until 5 years
medical observations up to age 5 (collection of follow-up as part of standard care) of newborns with positive results
Measured: 5 years
pGS-NBS performance
Children with positive results with pGS-NBS not confirmed by the diagnostic assessment
Measured: 3 months post pGS-NBS results delivery
pGS-NBS performance
Identification of one of the 14 diseases in the conventional NBS
Measured: frame 1 month after the birth
qualitative exploration
interviews
Measured: At : 1,6,12,24,36,48 and 60 months after positive results delivery At : 1 and 12 months after negative results delivery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Mar 2025
- Study start5 May 2025
- Primary completionMay 2027 (estimated)
- Study completionJul 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Newborn Screening Programmes for Rare DiseasesStudies of the same condition, open and under way.
- More trials run by Centre Hospitalier Universitaire DijonThe sponsor's other registered studies.
- 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
- 5,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Universitaire Dijon
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06875089
- Sponsor's protocol ID
- OLIVIER FAIVRE AFM 2023
- Acronym
- PGC1
- Status last verified
- Jun 2026
- First submitted
- 26 Feb 2025
- Last updated
- 17 Jun 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Level C, Thauvin-Robinet C, Binquet C, Duffourd Y, Davoine E, Chevarin M, Tran-Mau-Them F, Lemaitre M, Bruel AL, Safraou H, Salvi D, Tisserant E, Lecommandeur E, Charreton A, Hassine A, de Tayrac M, Redon R, Barc J, Schmitt S, Piard J, Kuentz P, Cormier C, Malbos M, Racine C, Chabrol B, Cheillan D, Tardy V, Colin E, Bris C, Mercier S, Nizon M, Gaudillat L, Loizeau V, Lenelle C, Mottet N, Simon E, Arnoux JB, Carpentier M, Renaud C, Ziegler A, Lejeune C, Jannot AS, Asensio ML, Rollier P, Odent S, Bezieau S, Pasquier L, Huet F, Faivre L. PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France. BMJ Open. 2025 Oct 23;15(10):e105752. doi: 10.1136/bmjopen-2025-105752.
PubMed 41130699
Study at a glance
From the registry record, last updated by the sponsor on 17 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Pilot Study to Assess the Feasibility and Acceptability of Newborn Screening Using in Silico Panel-based Solo Genome Sequencing in France PERIGENOMED-CLINICS 1 (PGC1 Study)
- ClinicalTrials.gov ID
- NCT06875089
- Acronym / sponsor ID
- PGC1 / OLIVIER FAIVRE AFM 2023
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 5,000 participants (estimated)
- Lead sponsor
- Centre Hospitalier Universitaire DijonUniversity, hospital or other
- Study start
- 5 May 2025 (actual)
- Primary completion
- May 2027 (estimated)
- Study completion
- Jul 2032 (estimated)
- First posted
- 13 Mar 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.
Newborn Screening (NBS) based on genome sequencing (GS) is currently the subject of particular attention at both European and international levels. Over the past three years, several publications have discussed the opportunities and challenges of using GS for NBS. To date, only two Chinese programs have published their results, the first on a series of 29,601 healthy newborns and the second on a series of 10,334 healthy newborns and 668 high-risk infants. Globally, more than twenty pilot projects are underway, although none has been initiated within the French context thus far. Across the different pilot projects, various study designs are used. Most have opted for a targeted GS-based analysis to screen for pediatric-onset diseases. Some projects focus solely on diseases for which effective drugs or interventions exist to prevent or reduce symptoms. In contrast, others offer parents the option to screen their newborns for diseases without current treatment options, but for which a treatment is underdevelopment, or with interest in early management, a choice exercised by most parents. Indeed, early diagnosis of these diseases can help to introduce treatments or interventions when they become available, to participate in research trials on new treatments and to receive early management and genetic counseling.
In France, the national NBS program has long been recognized worldwide for its organizational quality and comprehensiveness, although, until recently, it has one of the lowest numbers of diseases screened in Europe. As of mid-2024, the French NBS only includes 14 serious diseases. Recently, the French bioethics law has evolved to allow the use of genetic testing as a first-line procedure for NBS. At the same time, the development and efficiency of genomic techniques and the rapid increase in the number of treatable rare diseases (RDs) raise questions about the acceptability and relevance of these genomic methods for NBS and its possible extension. The extension of NBS to many RDs of early onset represents a real public health challenge as RDs, 80% of which are of genetic origin, account for 10% of deaths before the age of 5.
The FHU TRANSLAD has elaborated the PERIGENOMED Project, a large-scale project which aims to assess the relevance of pGS-NBS in France (analytical and clinical validity, clinical utility and psychosocial, ethical and organizational issues).
The pGS-NBS (also known as in silico panel-based GS, i.e. an analysis carried out entirely using informatic tools) consists of bioinformatics filtering steps that return only selected variants and/or rare variants from targeted genes issued from GS. So, even if the source data comes from the GS, it is possible to configure the pipeline to return only those variations known to be responsible for specific RDs.
the PERIGENOMED Project will be led in two steps. The first pilot step (PERIGENOMED-CLINICS 1 - PGC1 Study), presented in this protocol, aims to evaluate the feasibility and acceptability of pGS-NBS France. This pilot study plans to screen 2,500 newborns using pGS-NBS targeting two lists of genes (1 corresponding to genes variables responsible of treatable rare diseases, 2 including genes variation leading to actionable rare diseases). In both lists only RDs of early onset are considered. PGC1 study will be carried in 5 healthcare centers in France, with results expected to be returned to clinicians within less than 4 weeks. It will also provide an understanding of the optimal information and analytical pathways, and the possible organizational repercussions of pGS-NBS as well as a first insight about the validity of the pGS-NBS and about the clinical course of newborns screened positive and with a confirmed RD Two studies in humanities and social sciences (HSS) will also be linked to PGC1 Study. The first will focus on the reasons given by decliners and on the medical and socio-economic characteristics (at the individual and contextual level) of decliners versus participants. The second will assess the psychosocial impact of result disclosure on families of positive newborns, comparatively of negative ones.
These initial results will provide the first outcomes before the launch of a second larger phase PERIGENOMED-CLINICS 2 (PGC2 Study - 22,000 newborns), designed for studying the implementation of such pGS-NBS in routine on a regional level.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| No participants | – | Other: Satisfaction questionnaire, Other: interview with HSS researcherfuture families not taking part in the pGS- NBS study |
| Participants | – | Genetic: pGS-NBS, Other: Satisfaction questionnaire, Other: interview with HSS researcher, Other: Qualitative and quantitative longitudinal exploration, Other: Medical follow upfuture families who take part the pGS-NBS |
Who may qualify
- Ages
- 0 to 28 days
- Sex
- All
- Age groups
- Child
- Study population
- all the parents of live newborns in each participating maternity unit
Key inclusion criteria (14 listed)
- For satisfaction study about the information \& identification of determinants of acceptability :
- All future parents approached for whom the unborn child will be cared for in the participating maternity unit
- At least one parent/legal guardian who received information about the study
- Future parents/legal guardian who do not object to the use of their data
- Parent(s) or legal guardian(s) affiliated to a social security system or beneficiaries of such a system
Key exclusion criteria (4 listed)
- Parent(s) or legal guardian(s) under legal protection (guardianship, tutorship) or to a court order Non-inclusion criteria for newborn
- Babies born under anonymous birth according to the French law, known as "nés sous X"
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| pGS-NBSCollection of a second DBS card if the parents accept the pGS-NBS for their newborn | Genetic | Participants |
| Satisfaction questionnairequestionnaire on information process of parents informed about pGS-NBS | Other | No participants, Participants |
| interview with HSS researcherinterview with a member of the HSS team on reasons for declining /accepting pGS-NBS | Other | No participants, Participants |
| satisfaction questionnairequestionnaire on results delivery in parents having accepted the pGS-NBS | Other | Participants |
| Qualitative and quantitative longitudinal explorationvalidated anxiety and depression scales to assess the psychosocial impact and perceived utility for families whose child screened negative among which 30 families will be interviewed. Interviews and validated anxiety and depression scales will be suggested to all families receiving positive screening results | Other | Participants |
| Medical follow upfollow-up of true positives and false negatives based on medical records (vital status, care pathways) until 5 years after results delivery | Other | Participants |
Primary outcome
parents who have accepted the pGS-NBS for their children for Treatable list
Time frame: until 2 days after birth with extension up to 28 days in case of hospitalization in intensive care
number of families taking part the pGS-NBS (Treatable list) among the families who were offered the pGS-NBS in the centers over the inclusion period. If this number is at least of 603/1251, we will be able to reject that the percentage of acceptance is below 45% versus the alternative that it is greater Conversely, if the number is equal or below 602/1251, we will reject the hypothesis that the acceptability is at least 50%.
results concerning the Treatable list returned to clinicians within 4 weeks following the sample
Time frame: 4 weeks following the sample
number of families for which the pGS-NBS results concerning the Treatable list are delivered to clinicians in less than 4 weeks among those who consent to the pGS-NBS. If this number is at least 219/220, we will reject our null hypothesis (i.e. that the feasibility rate is less than or equal to 95% versus the alternative hypothesis that it is greater).
10 secondary outcomes
parents who have accepted the pGS-NBS for their children for Actionable list
Time frame: until 2 days after birth
results concerning the Actionable list returned to clinicians within 4 weeks following the sample,
Time frame: 4 weeks following the sample
Questionnaire for parents' satisfaction with the screening and reporting processes
Time frame: up to 4 weeks
profiles of parents who take part or not to pGS-NBS
Time frame: at the baseline
quantitative exploration
Time frame: At : 1,6,12,24,36,48 and 60 months after positive results delivery At : 1 and 12 months after negative results delivery
pGS-NBS performance
Time frame: 5 years;
Clinical evoluation of newborns with true positive results until 5 years
Time frame: 5 years
pGS-NBS performance
Time frame: 3 months post pGS-NBS results delivery
pGS-NBS performance
Time frame: frame 1 month after the birth
qualitative exploration
Time frame: At : 1,6,12,24,36,48 and 60 months after positive results delivery At : 1 and 12 months after negative results delivery
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 Jun 2026.
- Derived from this study: PubMed 41130699Level C, Thauvin-Robinet C, Binquet C, Duffourd Y, Davoine E, Chevarin M, Tran-Mau-Them F, Lemaitre M, Bruel AL, Safraou H, Salvi D, Tisserant E, Lecommandeur E, Charreton A, Hassine A, de Tayrac M, Redon R, Barc J, Schmitt S, Piard J, Kuentz P, Cormier C, Malbos M, Racine C, Chabrol B, Cheillan D, Tardy V, Colin E, Bris C, Mercier S, Nizon M, Gaudillat L, Loizeau V, Lenelle C, Mottet N, Simon E, Arnoux JB, Carpentier M, Renaud C, Ziegler A, Lejeune C, Jannot AS, Asensio ML, Rollier P, Odent S, Bezieau S, Pasquier L, Huet F, Faivre L. PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France. BMJ Open. 2025 Oct 23;15(10):e105752. doi: 10.1136/bmjopen-2025-105752.
- Individual participant dataSharing planned: Undecided
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.
5 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Newborn Screening Programmes for Rare Diseases, run by Centre Hospitalier Universitaire Dijon at 5 sites in France.
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 14 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 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 5 sites in France. 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 Laurence OLIVIER-FAIVRE (0380295313 ext. +33, laurence.faivre@chu-dijon.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
parents who have accepted the pGS-NBS for their children for Treatable list (time frame: until 2 days after birth with extension up to 28 days in case of hospitalization in intensive care). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06875089, which also lists 1 linked publication.
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 Jun 2026.