An Adaptive Clinical Trial of BeginNGS Newborn Screening for Hundreds of Genetic Diseases by Genome Sequencing

Genetic Disease Clinical Trial

— BeginNGS  

Official title:

An Adaptive Clinical Trial of BeginNGS Newborn Screening for Hundreds of Genetic Diseases by Genome Sequencing

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06306521
• Other study ID #: 20235517
• Status: Recruiting
• Phase: N/A
• Start date: February 29, 2024
• Est. completion date: February 2029

Study information

• Verified date: March 2024
• Source: Rady Pediatric Genomics & Systems Medicine Institute
• Contact: Lauren Olsen, MSN
• Phone: 858-576-1700
• Email: lolsen1[@]rchsd.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical trial is to test a new method for newborn screening using whole genome sequencing, called BeginNGS. Parents will be approached to provide informed consent to enroll their newborns in prenatal, postnatal, and outpatient settings. The main questions this study aims to answer are: What is the utility of BeginNGS as compared to state newborn screening? What is the acceptability and feasibility of BeginNGS as compared to state newborn screening? What is the cost effectiveness of BeginNGS as compared to state newborn screening? Enrolled newborns will have a blood sample taken and will receive the BeginNGS test. Newborns will have also had the state newborn screening test.

Description:

Each year 98% of US newborns receive screening (NBS) of dried blood spots (DBS) for at least 35 Recommended Uniform Screening Panel (RUSP) genetic disorders for diagnosis and treatment at/before onset of symptoms. About 6,600 true positive infants are identified per year. NBS is well-accepted and has proven clinical utility. Between 2010 and 2022, however, while many new therapeutic interventions for childhood genetic diseases showed clinical utility and/or were approved by the Food and Drug Administration (FDA), only 6 disorders were added to the RUSP. As a result, ~700 childhood genetic diseases have effective treatments but are not yet screened by NBS, and affected children experience delayed diagnosis and treatment, and poor outcomes. To solve this problem the investigators are developing BeginNGS - NBS by genome sequencing (GS) of DBS for, ultimately, ~700 severe, childhood genetic diseases with effective therapeutic interventions. BeginNGS is adaptive: genetic disorders are added (or removed) as evidence emerges that early treatment improves (or does not improve) outcomes. BeginNGS version 1 (v1, 388 genetic disorders) had good sensitivity (88.8%) and false positive rate (0.27%) in a retrospective study of 458,000 subjects. An exploratory prospective clinical trial comparing BeginNGS v2 (with 409 disorders) and rapid diagnostic genome sequencing (RDGS) identified reportable findings in 24 (34%) of 71 acutely ill newborns who were not suspected of having a genetic disease. Only 2 of those disorders were detected by standard NBS. The investigators propose a single group, multicenter, adaptive clinical trial to compare utility, acceptability, feasibility, and cost effectiveness of BeginNGS (experimental intervention) with standard NBS (control) in a minimum of 10,000 neonates (aged <28 days, maximum of 100,000). The primary objective of the trial is to generate evidence to support broad implementation of BeginNGS. An adaptive design was chosen rather than a traditional, fixed design to allow accumulating results to make the trial more efficient, informative, and ethical by addition or removal of BeginNGS disorders and genetic variants, population enrichment (for minority racial, ethnic, and ancestral groups), and sample size re-estimation. Adaptive design will also facilitate meta-analysis with other clinical trials of NBS-by-GS, providing greater power to test utility in ultra-rare genetic diseases. NBS-by-GS has the potential to transform the way childhood genetic diseases are diagnosed and treatments started. Preliminary data suggest that national adoption of BeginNGS in all births has the potential to improve outcomes of >50,000 US children per year.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 10000
• Est. completion date: February 2029
• Est. primary completion date: February 2029
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 1 Day to 28 Days

Eligibility

Inclusion Criteria:

1. Neonates (<28 days old) at enrollment sites.

2. Parents must have identified a primary care provider (or group).

Exclusion Criteria:

1. Neonates whose mother is less than 18 years of age.

2. Neonates who are wards of the state.

3. Neonates whose parent/legal guardian is unable to provide consent.

4. Parents with a home address outside the US or jurisdiction of the enrollment sites.

5. Neonates or fetuses who are ill and in whom enrollment or sampling is anticipated to interfere with healthcare provision at delivery. For example, fetuses or neonates who are likely to require transfer to a higher level of care, such as to a Level IV NICU upon delivery.

6. Neonates who are under consideration for a rapid diagnostic genome sequence or other diagnostic genetic testing.

7. Neonates who are not expected to survive the neonatal period.

Related Conditions & MeSH terms

• Genetic Disease
• Genetic Diseases, Inborn

Intervention

Genetic:
• BeginNGS Test
Genomic sequencing that screens for over 400 genetic diseases.

Locations

Country	Name	City	State
United States	Rady Children's Hospital San Diego	San Diego	California

Sponsors (1)

Lead Sponsor	Collaborator
Rady Pediatric Genomics & Systems Medicine Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comparison of the clinical utility of BeginNGS and standard of care (state NBS), defined by the proportion of enrollees likely to benefit (likely to have an improved outcome) from an indicated therapeutic intervention	The proportion of enrollees likely to benefit (likely to have an improved outcome) from an indicated therapeutic intervention (as per an electronic clinical management system, Genome-to-Treatment, GTRx)	5 years
Secondary	Utility secondary outcome 1	The proportion of BeginNGS and state NBS of DBS that are positive (Positive rate)	5 years
Secondary	Utility secondary outcome 2	The proportion of BeginNGS and state NBS of DBS positive results that are confirmed (true positive rate and positive predictive value)	5 years
Secondary	Utility secondary outcome 3	The proportion of BeginNGS and state NBS of DBS that are true positive and diagnosed during infancy.	5 years
Secondary	Utility secondary outcome 4	The proportion of BeginNGS and state NBS of DBS that are true positive and diagnosed at study end.	5 years
Secondary	Utility secondary outcome 5	The proportion of BeginNGS and state NBS of DBS that are positive and in whom an indicated therapeutic intervention was commenced by study end.	5 years
Secondary	Utility secondary outcome 6	The proportion of BeginNGS and state NBS of DBS that are positive and in whom a disease outcome changed due to a therapeutic intervention by study end.	5 years
Secondary	Utility secondary outcome 7	Subgroup analysis of clinical utility (as defined by the primary outcome measure) by race (black, white, Asian), ethnicity (Hispanic, non-Hispanic), genetic ancestry, and disorder group	5 years
Secondary	Utility secondary outcome 8	Subgroup analysis of positive rate (secondary utility outcome measure 1) by race, ethnicity, genetic ancestry, and disorder group.	5 years
Secondary	Utility secondary outcome 9	Subgroup analysis of true positive rate (secondary utility outcome measure 2) by race, ethnicity, genetic ancestry, and disorder group.	5 years
Secondary	Utility secondary outcome 10	Subgroup analysis of the proportion of BeginNGS and state NBS of DBS that are true positive and diagnosed during infancy in infancy by race, ethnicity, genetic ancestry, and disorder group.	5 years
Secondary	Acceptability outcome 1	Proportion of parents approached who agree to enroll their newborn (Figure 1c?). This is a "key outcome" (as defined by CONSORT PRO31).	5 years
Secondary	Acceptability outcome 2	Physician and parental questionnaires (Figure 1c?) regarding perceptions of benefits and harms of BeginNGS by parents and primary care pediatricians.	5 years
Secondary	Acceptability outcome 3	Subgroup analysis of enrollment rate (proportion of parents approached who agree to enroll their newborn; Figure 1c?) by race, ethnicity, genetic ancestry, and enrollment method.	5 years
Secondary	Acceptability outcome 4	Subgroup analysis of parental questionnaires (regarding perceptions of benefits and harms of BeginNGS) by race, ethnicity, and genetic ancestry.	5 years
Secondary	Feasibility (ability of the study to be undertaken as designed) outcome 1	Time to return of a result for BeginNGS and state NBS.	5 years
Secondary	Feasibility (ability of the study to be undertaken as designed) outcome 2	Time to return of a confirmed true positive result of BeginNGS and state NBS.	5 years
Secondary	Feasibility (ability of the study to be undertaken as designed) outcome 3	Proportion of enrollees with positive results who undergo confirmatory testing by BeginNGS and state NBS.	5 years
Secondary	Feasibility (ability of the study to be undertaken as designed) outcome 4	Time to diagnosis (time until a clinical feature of the disorder is identified) for BeginNGS and state NBS.	5 years
Secondary	Feasibility (ability of the study to be undertaken as designed) outcome 5	Proportion of enrollees lost to follow up at one year of age.	5 years
Secondary	Cost effectiveness outcome 1	Average cost effectiveness ratio (ACER, average cost to prevent one infant death or adverse event).	5 years
Secondary	Cost effectiveness outcome 2	Incremental cost effectiveness ratio (ICER, average change in cost associated with prevention of one infant death or adverse event).	5 years
Secondary	Cost effectiveness outcome 3	Subgroup analysis of Average Cost Effectiveness Ratio (ACER, average cost to prevent one infant death or adverse event) by disorder group (for example metabolic disorders, immunodeficiency disorders, seizure disorders, endocrine disorders, vitamin and cofactor deficiency disorders, hematologic disorders, muscle disorders).	5 years
Secondary	Cost effectiveness outcome 4	Subgroup analysis of Incremental cost effectiveness ratio (ICER, average change in cost associated with prevention of one infant death or adverse event) by disorder group (for example metabolic disorders, immunodeficiency disorders, seizure disorders, endocrine disorders, vitamin and cofactor deficiency disorders, hematologic disorders, muscle disorders).	5 years
Secondary	Accuracy outcome 1	True positive rate (true positive/true positive+false negative, recall, sensitivity) of BeginNGS by comparison with state NBS of DBS (all enrollees).	5 years
Secondary	Accuracy outcome 2	True positive rate of BeginNGS by comparison with other genetic tests (in infants who subsequently receive diagnostic testing for a suspected genetic disease).	5 years
Secondary	Utility secondary outcome 11	Number needed to screen to prevent one infant death or adverse event.	5 years
Secondary	Feasibility outcome 6	Incidence of variants and haplotypes associated with individual genetic diseases in newborns.	5 years
Secondary	Feasibility outcome 7	Categorical determination of genetic pattern of inheritance (for example dominant, recessive) of individual genetic diseases in newborns (where this has not been unequivocally established).	5 years
Secondary	Utility secondary outcome 12	Subgroup categorical analysis of efficacy of individual therapeutic interventions in infants.	5 years