National Human Genome Research Institute (NHGRI)
Open enrollment with an early-phase pipeline tilt
According to ClinicalTrials.gov-derived indexes, National Human Genome Research Institute (NHGRI) sits in the top decile of US sponsors by registered trial count (#161 of 15,742 sponsors by registered trial count).
National Human Genome Research Institute (NHGRI): 185 sponsored US clinical trials, 30 recruiting.
National Human Genome Research Institute (NHGRI) sponsors 185 registered US clinical trials on ClinicalTrials.gov, 30 of them currently recruiting, and 143 completed. 0 of these trials are in Phase 3-4 (later-stage) and 18 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Proteus Syndrome, with 3 trials.
Top-decile sponsor footprint
National Human Genome Research Institute (NHGRI) ranks in the top decile of sponsors by registered trial count (#161 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.
Trial completion reliability score
143 of 152 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (94.1%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.
Open and recent trials
185 total, page 1 of 4
Deciphering the Genetic Architecture of Autoimmune Diseases
NCT06948110
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405
An Open-Label Phase 2 Study of N-Acetyl-D-Mannosamine (ManNAc) in Subjects With Primary Focal Segmental Glomerulosclerosis
NCT06664814
Cybersickness Prevention and Mitigation in Virtual Reality for Healthy Volunteers
NCT06552754
Study to Understand the Genetic Risk of Developing an Immune Response After Blood Transfusions Among Individuals With Sickle Cell Disease
NCT06944067
Childhood-Onset Essential Hypertension Natural History Study
NCT06778239
A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders
NCT06092346
Caregiving Networks Across Disease Context and the Life Course
NCT05007990
MK-7075 (Miransertib) in Proteus Syndrome
NCT04316546
Acute Infection in Mitochondrial Disease: Metabolism, Infection and Immunity
NCT04419870
IDENTIFY Study: Natural History of Maternal Neoplasia
NCT04049604
A Phase 1/2 Study of Intravenous Gene Transfer With an AAV9 Vector Expressing Human Beta-galactosidase in Type I and Type II GM1 Gangliosidosis
NCT03952637
Longitudinal Studies of Patient With FPDMM
NCT03854318
Natural History, Physiology, Microbiome and Biochemistry Studies of Propionic Acidemia
NCT02890342
Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
NCT02450851
Genomic Services Research Program
NCT02595957
Clinical and Basic Investigations Into Known and Suspected Congenital Disorders of Glycosylation
NCT02089789
The NIH MINI Study: Metabolism, Infection, and Immunity in Inborn Errors of Metabolism
NCT01780168
A Natural History Study of Patients With GNE Myopathy and GNE-Related Diseases
NCT01417533
Genome Medical Sequencing for Gene Discovery
NCT01087320
Studies of Skin Microbes in Healthy People and in People With Skin Conditions
NCT00605878
Clinical and Laboratory Study of Methylmalonic Acidemia
NCT00078078
Study of Chediak-Higashi Syndrome
NCT00005917
Natural History of Glycosphingolipid Storage Disorders and Glycoprotein Disorders
NCT00029965
Study of Alkaptonuria
NCT00005909
Clinical and Basic Investigations Into Hermansky-Pudlak Syndrome
NCT00001456
Study of Proteus Syndrome and Related Congenital Disorders
NCT00001403
Familial Mediterranean Fever and Related Disorders: Genetics and Disease Characteristics
NCT00001373
Use of Cysteamine in the Treatment of Cystinosis
NCT00359684
Diagnosis and Treatment of Patients With Inborn Errors of Metabolism
NCT00369421
ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study
NCT00410241
Analysis of Specimens From Individuals With Pulmonary Fibrosis
NCT00084305
Natural History Study of Smith-Magenis Syndrome
NCT00013559
Care Choreographies and the Making of the Psychosocial in Genetic Counseling
NCT06280833
Genomics, Environmental Factors and Social Determinants of Cardiovascular Disease in African-Americans Study (GENE-FORECAST): Prospective COVID-19 Natural History Study
NCT05484882
Genetic and Social Network Correlates of Rheumatoid Arthritis Outcomes in Hispanic Populations: A Prospective Study
NCT05457816
Living With Sickle Cell Disease in the COVID-19 Pandemic
NCT04417673
Genetics of COVID-19 Susceptibility and Manifestations
NCT04371432
New Approaches for Empowering Studies of Asthma in Populations of African Descent
NCT03937804
Mapping Institutional Identities and the Production of Ethics
NCT03983863
Adult Patients With Undiagnosed Conditions and Their Responses to Clinically Uncertain Results From Exome Sequencing
NCT03605004
Study of People With Generalized Arterial Calcification of Infancy (GACI) or Autosomal Recessive Hypophosphatemic Rickets Type 2 (ARHR2)
NCT03478839
Is it Feasible?: Self-Affirmation for Hereditary Breast and Ovarian Cancer Genetic Counseling
NCT03225170
Pregnant Women s Views About the Ethics of Prenatal Whole Genome Sequencing
NCT03105492
Examining the Knowledge, Attitudes, and Beliefs of Sickle Cell Disease Patients, Parents of Patients With Sickle Cell Disease, and Providers Towards the Integration of CRISPR in Clinical Care
NCT03167450
Where Culture Meets Genetics: Exploring Latinas Causal Attributions of Breast and Colon Cancer and Models of Disease Inheritance
NCT02767986
New Technology and Child Health
NCT02622035
Dose Finding Trial of MK-7075 in Children and Adults With Proteus Syndrome
NCT02594215
Are Genetic Counselors Screening for Adolescent Suicide Risk?
NCT02486120
Study of Sirolimus Therapy for Segmental Overgrowth Caused by Somatic PI3K Activation
NCT02428296
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 11 |
| Phase 2 | 7 |
Therapeutic Areas
What is open in the National Human Genome Research Institute (NHGRI) pipeline
30 recruiting of 185 indexed (16% open); 143 completed (77%).
Phase mix: 0 late (III/IV) vs 18 early (I/II) (early-phase heavy).
Top condition: Proteus Syndrome (3 trials), 9 others listed.
How open-pipeline share is computed
Recruiting share is recruiting_count divided by trial_count for this sponsor in the public registry export. Status can change between pulls; treat the figure as a research-attention snapshot, not product availability.
National Human Genome Research Institute (NHGRI): open-pipeline peers nationwide
Peers matched on 185 registered trials and 16% open enrollment, not the therapeutic-area sidebar.
National Human Genome Research Institute (NHGRI) sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together.
Sponsors near 185 trials (± recruiting share)
- Boston University · 185 trials · 12% recruiting
- Children's Mercy Hospital Kansas City · 184 trials · 11% recruiting
- Arizona State University · 187 trials · 15% recruiting
- Johns Hopkins Bloomberg School of Public Health · 187 trials · 14% recruiting
Sponsors near 16% open enrollment (± trial volume)
- BioMarin Pharmaceutical · 16% recruiting · 80 trials
- Atlantic Health System · 16% recruiting · 43 trials
- Drexel University · 16% recruiting · 92 trials
- Case Western Reserve University · 16% recruiting · 141 trials
Related
What to do with this National Human Genome Research Institute (NHGRI) page
185 registered trials is a research-attention snapshot, not an endorsement of National Human Genome Research Institute (NHGRI) or any single study.
- 30 of National Human Genome Research Institute (NHGRI)'s trials are currently recruiting, check each one's own eligibility criteria before contacting a site. Browse recruiting trials
- Proteus Syndrome is the condition National Human Genome Research Institute (NHGRI) studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Proteus Syndrome trials
- Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide
Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.
National Human Genome Research Institute (NHGRI) pipeline card: 185 registered trials from official public datasets.Report a data error.