Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 60/100

Failure Rate

13.3%

4 terminated/withdrawn out of 30 trials

Success Rate

82.6%

-3.9% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

47%

9 of 19 completed trials have results

Key Signals

1 recruiting9 with results

Enrollment Performance

Analytics

Phase 1
18(72.0%)
Phase 2
7(28.0%)
25Total
Phase 1(18)
Phase 2(7)

Activity Timeline

Global Presence

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Clinical Trials (30)

Showing 20 of 30 trials
NCT06980948Phase 1Recruiting

Safety and Tolerability Study of ST-503 for Refractory Pain Due to Peripheral Neuropathy (Small Fiber Predominant, SFN)

Role: lead

NCT04046224Phase 1Completed

Dose-Ranging Study of ST-920, an AAV2/6 Human Alpha Galactosidase A Gene Therapy in Subjects With Fabry Disease (STAAR)

Role: lead

NCT05987527Active Not Recruiting

Long-Term Follow-Up of TX200-TR101 (STEADFAST Long Term)

Role: lead

NCT05145062Active Not Recruiting

Long - Term Follow Up of Sickle Cell Disease and Beta-thalassemia Subjects Previously Exposed to BIVV003 or ST-400.

Role: lead

NCT02500849Phase 1Active Not Recruiting

Safety Study of Zinc Finger Nuclease CCR5-modified Hematopoietic Stem/Progenitor Cells in HIV-1 Infected Patients

Role: collaborator

NCT03653247Phase 1Completed

A Study to Assess the Safety, Tolerability, and Efficacy of BIVV003 for Autologous Hematopoietic Stem Cell Transplantation in Patients With Severe Sickle Cell Disease

Role: lead

NCT05039866Enrolling By Invitation

Long-Term Follow-up of Subjects Who Were Treated With ST-920

Role: lead

NCT04817774Phase 1Active Not Recruiting

Safety & Tolerability Study of Chimeric Antigen Receptor T-Reg Cell Therapy in Living Donor Renal Transplant Recipients

Role: lead

NCT02695160Phase 1Terminated

Ascending Dose Study of Genome Editing by Zinc Finger Nuclease Therapeutic SB-FIX in Subjects With Severe Hemophilia B

Role: lead

NCT04628871Active Not Recruiting

Long Term Follow-up (LTFU) of Subjects Who Received SB-318, SB-913, or SB-FIX

Role: lead

NCT04201782Terminated

Long-term Follow-up of HIV Subjects Exposed to SB-728-T or SB-728mR-T

Role: lead

NCT03432364Phase 1Completed

A Study to Assess the Safety, Tolerability, and Efficacy of ST-400 for Treatment of Transfusion-Dependent Beta-thalassemia (TDT)

Role: lead

NCT02702115Phase 1Terminated

Ascending Dose Study of Genome Editing by the Zinc Finger Nuclease (ZFN) Therapeutic SB-318 in Subjects With MPS I

Role: lead

NCT00400634Phase 2Completed

Double-Blind, Multicenter, Sham Surgery Controlled Study of CERE-120 in Subjects With Idiopathic Parkinson's Disease

Role: lead

NCT00087789Phase 1Completed

CERE-110 in Subjects With Mild to Moderate Alzheimer's Disease

Role: lead

NCT00252850Phase 1Completed

Safety of CERE-120 (AAV2-NTN) in Subjects With Idiopathic Parkinson's Disease

Role: lead

NCT03041324Phase 1Terminated

Ascending Dose Study of Genome Editing by the Zinc Finger Nuclease (ZFN) Therapeutic SB-913 in Subjects With MPS II

Role: lead

NCT01079325Phase 2Completed

Clinical Trial of SB-509 in Subjects With Diabetic Neuropathy

Role: lead

NCT01543152Phase 1Completed

Dose Escalation Study of Cyclophosphamide in HIV-Infected Subjects on HAART Receiving SB-728-T

Role: lead

NCT02225665Phase 1Completed

Repeat Doses of SB-728mR-T After Cyclophosphamide Conditioning in HIV-Infected Subjects on HAART

Role: lead