Sequenom
Trial Pipeline
Non-Invasive Preeclampsia Screening and Biobank
NCT06643741
Clinical Follow-up of Pregnant Subjects Undergoing NIPT
NCT04595201
Compliant Analysis of Patient Samples and Data
NCT04364503
Specimen Collection from Patients with Non-Hematologic Cancer for Use in Development of a Liquid Biopsy Assay
NCT02586389
Specimen Collection from Pregnant Women At Increased Risk for Fetal Aneuploidy
NCT01429389
The Effect of Guided Care With Vectra Compared to Treatment as Usual in Patients With Rheumatoid Arthritis
NCT03631225
Genetic Analysis of Chronic Central Serous Chorioretinopathy Masquerading as Neovascular AMD
NCT01880788
Genetic Load and Phenotype in Aggressive AMD
NCT01650948
Clinical Evaluation of the SEQureDx T21 Test In High Risk Pregnancies
NCT01555346
Noninvasive Screening for Fetal Aneuploidy: A New Maternal Plasma Marker
NCT00971334
Evaluation of Fetal Sex in Assisted Reproductive Technology (ART) Achieved Pregnancies
NCT01021085
Development of a Fetal Sex Assay From Maternal Whole Blood
NCT00970047
What the Pipeline for Sequenom Shows
According to the ClinicalTrials.gov registry, Sequenom is linked to 43 US clinical trials across every stage of research activity. Of those, 36 studies are currently recruiting — about 84% of the sponsor's indexed portfolio — and 6 are already marked complete, representing roughly 14% of the total. Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
The phase mix for Sequenom reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2). A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work — safety, dosing, and early signal detection — and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
The top therapeutic focus area indexed for Sequenom is Down Syndrome with 3 linked trials, and 9 other condition areas appear in the top list above. That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice — verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology — how this data is sourced, computed, and verified.