Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

7.7%

1 terminated/withdrawn out of 13 trials

Success Rate

90.9%

+4.4% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

0%

0 of 10 completed trials have results

Key Signals

1 recruiting

Enrollment Performance

Analytics

Phase 1
9(69.2%)
Phase 2
4(30.8%)
13Total
Phase 1(9)
Phase 2(4)

Activity Timeline

Global Presence

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Clinical Trials (13)

Showing 13 of 13 trials
NCT07677683Phase 2Recruiting

STP705 Injection for Submental Fat Reduction

Role: lead

NCT05037149Phase 1Completed

Ph. 1, Evaluation of Safety, Tolerability, PK, Anti-tumor Activity of STP707 IV in Subjects With Solid Tumors

Role: lead

NCT05196373Phase 1Withdrawn

Safety, Tolerability, Pharmacokinetics, Immunogenicity and Efficacy of STP705 in Adult Patients With Hypertrophic Scars

Role: lead

NCT05844293Phase 1Active Not Recruiting

Single Ascending Dose of FXI-GalNAc-siRNA in Healthy Subjects

Role: lead

NCT04844840Phase 2Completed

A Study for Safety and Efficacy Evaluation of Various Doses of STP705 in Reducing Keloid Recurrence

Role: lead

NCT04676633Phase 1Completed

Safety, Tolerability, PK, Anti-Tumor Activity of STP705 in Subjects With Advanced/Metastatic or Surgically Unresectable Solid Tumors Who Are Refractory to Standard Therapy

Role: lead

NCT05422378Phase 1Completed

A Study to Evaluate Safety, Tolerability of Subcutaneous Injection in Adult Subjects Undergoing Abdominoplasty

Role: lead

NCT04669808Phase 2Completed

Open Label, Dose Escalation Study for the Safety and Efficacy of STP705 in Adult Patients With Basal Cell Carcinoma

Role: lead

NCT05421013Phase 1Completed

Study to Evaluate Safety, Efficacy of Intralesional Injection of STP705 in Adults With Facial isSCC

Role: lead

NCT04844983Phase 2Completed

A Study to Evaluate Safety, Efficacy of Intralesional Injection of STP705 in Patients With isSCC

Role: lead

NCT05309915Phase 1Completed

A Study of STP707 Administered by IV in Healthy Subjects

Role: lead

NCT04293679Phase 1Completed

Open Label, Dose Escalation Study for the Safety and Efficacy of STP705 in Adult Patients With isSCC

Role: lead

NCT02956317Phase 1Completed

A Randomized Study to Evaluate the Safety and Efficacy of Various Doses of STP705 in Subjects With Hypertrophic Scar

Role: lead

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