Natera, Inc. (NTRA)
Natera, Inc. is a diagnostics company focused on developing and commercializing a wide array of molecular testing services globally. Its portfolio includes several key offerings: Panorama, a non-invasive prenatal test (NIPT) that screens for chromosomal abnormalities in a fetus using a blood sample from the mother, and also determines zygosity in twin pregnancies. Vistara, designed to identify single-gene disorders by screening for specific single-gene mutations. Horizon, a comprehensive carrier screening test to determine an individual's carrier status for various genetic diseases. Spectrum, utilized during in vitro fertilization (IVF) cycles to detect chromosomal anomalies or inherited genetic conditions. Anora, a miscarriage analysis product that examines fetal chromosomes to help understand the cause of pregnancy loss. Non-invasive paternity testing, which establishes paternity during gestation using blood samples from both the pregnant mother and the alleged father. Beyond reproductive health, Natera also provides specialized tests: Signatera, a sophisticated circulating tumor DNA (ctDNA) technology capable of screening for a generic set of mutations, independent of the individual's specific tumor characteristics. Prospera, a test used to assess and monitor organ transplant rejection. Additionally, the company offers Constellation, a cloud-based software platform that provides laboratory clients with access to Natera's proprietary algorithms and bioinformatics, enabling them to validate and launch their own tests. Natera distributes its products through a direct sales team and an extensive network of approximately 100 laboratory and distribution partners. The company has strategic partnerships, including one with BGI Genomics Co., Ltd. for the development, manufacturing, and commercialization of NGS-based genetic testing assays, and another with Foundation Medicine, Inc. to develop and commercialize personalized circulating tumor DNA monitoring assays. Founded in 2003, Natera, Inc. is headquartered in Austin, Texas. It was formerly known as Gene Security Network, Inc. before changing its name in 2012.
Sector: Services-Medical Laboratories
Industry: Medical - Diagnostics & Research
Natera, Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 4Terminated
Impact of Parental Support on Pregnancy Outcomes (IPSO) Trial- Day 3 Preimplantation Genetic Screening (PGS) With Day 5 Fresh Transfer
24 Chromosome Aneuploidy Screening with Parental Support
Preimplantation Gentic Screening (PGS), In Vitro Fertilization (IVF) +1
NCT01194531Enrollment59StartSep 2010Primary CompletionApr 2013CompletionApr 2013 - Not applicableCompleted
Concurrent Single Gene and 24 Chromosome Aneuploidy Preimplantation Genetic Diagnosis (PGD)
preimplantation diagnosis
Any Single Gene Disorder (Cystic Fibrosis, Tay-Sachs)
NCT01023048Enrollment56StartNov 2009Primary CompletionMar 2014CompletionMar 2014 - ObservationalCompleted
Clinical Use of Parental Support To Detect Single Gene Mutations
Preimplantation Genetic Diagnosis
Single Gene Disorders
NCT01197872Enrollment240StartSep 2010Primary CompletionJun 2013CompletionJun 2013 - ObservationalTerminated
Prenatal Non-invasive Aneuploidy Test Utilizing SNPs Trial
Blood Draw
Trisomy 13, Trisomy 18 +2
NCT01545674Enrollment937StartJan 2012Primary CompletionApr 2014CompletionMar 2023 - ObservationalCompleted
Collection of Maternal Blood Samples for Development of Non-invasive Prenatal Diagnostic Testing
Blood draw
Pregnancy Following IVF With PGS/PGD
NCT01546324Enrollment16StartFeb 2012Primary CompletionMay 2012CompletionAug 2013 - ObservationalCompleted
Non-invasive Prenatal Diagnostic Validation Study
Blood draw, Cheek swab/Saliva Sampling
Chromosome 13 Aneuploidy, Chromosome 18 Aneuploidy +3
NCT01574781Enrollment1,781StartSep 2011Primary CompletionApr 2013CompletionApr 2013 - ObservationalWithdrawn
Multi-disease Carrier Screening Test Validation
Blood draw
Spinal Muscular Atrophy (SMA), Carrier Screening +1
NCT01663584Enrollment0StartAug 2012Primary CompletionJun 2013Completion- - ObservationalCompleted
Development of Non-invasive Prenatal Screening Test for Microdeletions Based on Fetal DNA Isolated From Maternal Blood
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Trisomy 21, Trisomy 18 +3
NCT01852708Enrollment1,059StartNov 2012Primary CompletionOct 2020CompletionOct 2020 - ObservationalCompleted
Development of Non-invasive Prenatal Test for Microdeletion and Other Genetic Syndromes Based on Cell Free DNA
-
Microdeletion Syndromes, Trisomy 21 +3
NCT02109770Enrollment216StartOct 2012Primary CompletionJun 2019CompletionAug 2019 - ObservationalCompleted
Multiple Gestation Study
-
Trisomy 13, Trisomy 18 +2
NCT02278536Enrollment354StartMar 2013Primary CompletionMar 2019CompletionMar 2019 - ObservationalCompleted
High Risk Multiple Gestation Study
-
Trisomy 13, Trisomy 18 +2
NCT02278874Enrollment99StartAug 2014Primary CompletionDec 2018CompletionMar 2019 - ObservationalCompleted
SNP-based Microdeletion and Aneuploidy RegisTry (SMART)
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22q11 Deletion Syndrome, DiGeorge Syndrome +9
NCT02381457Enrollment20,960StartApr 2015Primary CompletionJun 2020CompletionJun 2020 - ObservationalTerminated
Natera Ovarian Cancer Detection Assay
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Adnexal Mass
NCT03485651Enrollment12StartDec 2017Primary CompletionNov 2019CompletionDec 2019 - ObservationalCompleted
Study for the Prediction of Active Rejection in Organs Using Donor-derived Cell-free DNA Detection
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Transplant Rejection, Allograft Rejection +1
NCT03984747Enrollment110StartSep 2018Primary CompletionAug 2024CompletionAug 2024 - ObservationalActive, not recruiting
The PROspera Kidney Transplant ACTIVE Rejection Assessment Registry (ProActive)
Prospera
Kidney Transplant Rejection
NCT04091984Enrollment5,000StartNov 2019Primary CompletionOct 2026est.CompletionOct 2027est. - ObservationalUnknown status
BESPOKE Study of ctDNA Guided Therapy in Colorectal Cancer
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Colorectal Cancer, Colon Cancer
NCT04264702Enrollment1,788StartApr 2020Primary CompletionSep 2025est.CompletionSep 2025est. - ObservationalCompleted
BESPOKE Study of ctDNA Guided Immunotherapy
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Colorectal Cancer, Melanoma +1
NCT04761783Enrollment290StartMay 2021Primary CompletionDec 2023CompletionMar 2024 - ObservationalCompleted
Verification of Risk Assignment for Whole Chromosome Using SNP-based NIPT in Vanishing Twin Pregnancies
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Vanishing Twin, Trisomy 21 +2
NCT05004337Enrollment136StartJul 2021Primary CompletionNov 2023CompletionNov 2023 - Not applicableWithdrawn
Donor-Derived Cell-free DNA to DETect REjection in Cardiac Transplantation
Prospera Transplant Assessment, Endomyocardial biopsy
Heart Transplant Failure and Rejection
NCT05081739Enrollment0StartJan 2023est.Primary CompletionJan 2025est.CompletionJan 2026est. - ObservationalActive, not recruiting
LAMBDA 002 (Lung Registry) Study
Prospera
Lung Transplant Rejection
NCT05170425Enrollment154StartNov 2022Primary CompletionAug 2026est.CompletionMay 2027est. - ObservationalActive, not recruiting
Prospera Test Evaluation in Cardiac Transplant (ProTECT)
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Heart Transplant Rejection
NCT05205551Enrollment411StartOct 2021Primary CompletionOct 2026est.CompletionJun 2027est. - ObservationalCompleted
Development of Non-invasive Cell-free DNA to Supplant Invasive Biopsy in Heart Transplantation
Prospera
Heart Transplant
NCT05309382Enrollment147StartDec 2022Primary CompletionOct 2024CompletionOct 2024 - ObservationalCompleted
Clinical Utility of the Addition of a SNP-based NIPT Zygosity Determination in Twin Pregnancy Management.
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Twin to Twin Transfusion Syndrome, Pregnancy Complications +1
NCT05312814Enrollment137StartOct 2021Primary CompletionMay 2023CompletionMay 2023 - Not applicableUnknown status
Renasight Clinical Application, Review and Evaluation (RenaCARE) Study
Renasight
Kidney Diseases
NCT05846113Enrollment1,720StartJun 2021Primary CompletionAug 2025est.CompletionAug 2025est. - Not applicableActive, not recruiting
A Comparative Effectiveness Study in Heart Transplant Patients of Rejection Surveillance With Cell-free DNA Versus Endomyocardial Biopsy
The Prospera™ Test
Heart Transplant Failure and Rejection
NCT06414603Enrollment250StartJun 2024Primary CompletionFeb 2027est.CompletionFeb 2027est.
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 4 | Terminated | 24 Chromosome Aneuploidy Screening with Parental Support | NCT01194531 |
| Not applicable | Completed | preimplantation diagnosis | NCT01023048 |
| Observational | Completed | Preimplantation Genetic Diagnosis | NCT01197872 |
| Observational | Terminated | Blood Draw | NCT01545674 |
| Observational | Completed | Blood draw | NCT01546324 |
| Observational | Completed | Blood draw, Cheek swab/Saliva Sampling | NCT01574781 |
| Observational | Withdrawn | Blood draw | NCT01663584 |
| Observational | Completed | - | NCT01852708 |
| Observational | Completed | - | NCT02109770 |
| Observational | Completed | - | NCT02278536 |
| Observational | Completed | - | NCT02278874 |
| Observational | Completed | - | NCT02381457 |
| Observational | Terminated | - | NCT03485651 |
| Observational | Completed | - | NCT03984747 |
| Observational | Active, not recruiting | Prospera | NCT04091984 |
| Observational | Unknown status | - | NCT04264702 |
| Observational | Completed | - | NCT04761783 |
| Observational | Completed | - | NCT05004337 |
| Not applicable | Withdrawn | Prospera Transplant Assessment, Endomyocardial biopsy | NCT05081739 |
| Observational | Active, not recruiting | Prospera | NCT05170425 |
| Observational | Active, not recruiting | - | NCT05205551 |
| Observational | Completed | Prospera | NCT05309382 |
| Observational | Completed | - | NCT05312814 |
| Not applicable | Unknown status | Renasight | NCT05846113 |
| Not applicable | Active, not recruiting | The Prospera™ Test | NCT06414603 |
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