Key Insights

Highlights

Success Rate

71% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 37/100

Termination Rate

11.8%

2 terminated out of 17 trials

Success Rate

71.4%

-15.1% vs benchmark

Late-Stage Pipeline

12%

2 trials in Phase 3/4

Results Transparency

80%

4 of 5 completed with results

Key Signals

4 with results71% success

Data Visualizations

Phase Distribution

11Total
Not Applicable (8)
P 2 (1)
P 3 (2)

Trial Status

Completed5
Recruiting4
Unknown4
Terminated2
Active Not Recruiting1
Enrolling By Invitation1

Trial Success Rate

71.4%

Benchmark: 86.5%

Based on 5 completed trials

Clinical Trials (17)

Showing 17 of 17 trials
NCT07563218Not ApplicableRecruitingPrimary

I-TOPS With Patients With Genetic Syndrome SYN-TOPS

NCT03420274Not ApplicableCompleted

Ensuring Patients' Informed Access to Noninvasive Prenatal Testing

NCT06125093Not ApplicableCompletedPrimary

Study of an Early Parenting Intervention for Children With Genetic Abnormalities and Mental Health Problems

NCT06666777Not ApplicableRecruiting

Speech Therapy and Parenting for Early Socio-communicAtive sKills

NCT03458962Recruiting

Diagnostic Odyssey: Whole Genome Sequencing (WGS)

NCT01255358Phase 2Completed

Intra-Erythrocyte Dexamethasone Sodium Phosphate in Ataxia Teleangiectasia Patients

NCT03563053Phase 3Terminated

Extension Treatment Using EryDex System in Patients With AT Who Participated in the ATTeST-IEDAT-02-2015 Study

NCT03967743Recruiting

Application of a Systematic Developmental Assessment to a Novel Population: Infants With Rare Genetic Disorders

NCT02770807Phase 3Completed

Intra-Erythrocyte Dexamethasone Sodium Phosphate in Ataxia Telangiectasia Patients

NCT03211039Not ApplicableActive Not Recruiting

Perinatal Precision Medicine

NCT03834987TerminatedPrimary

NGLY1 Deficiency: A Prospective Natural History Study

NCT03385876Not ApplicableEnrolling By Invitation

Rapid Whole Genome Sequencing Study

NCT03918707Unknown

Utility of Rapid Whole Genome Sequencing in the NICU: A Pilot Study

NCT03902353Not ApplicableUnknown

Screening of Pulmonary Veino Occlusive Disease in Heterozygous EIF2AK4 Mutation Carriers

NCT03642405Unknown

Drug-induced Repolarization ECG Changes

NCT02704260Not ApplicableCompletedPrimary

Genetic of SportS Induced Endofibrotic Remodeling

NCT03222947Unknown

New Variants Involved in Taybi-Linder Syndrome

Showing all 17 trials

Research Network

Activity Timeline