Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

0.0%

0 terminated/withdrawn out of 14 trials

Success Rate

100.0%

+13.5% vs industry average

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

0%

0 of 11 completed trials have results

Key Signals

1 recruiting

Enrollment Performance

Analytics

N/A
14(100.0%)
14Total
N/A(14)

Activity Timeline

Global Presence

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Clinical Trials (14)

Showing 14 of 14 trials
NCT07533461Not ApplicableCompleted

Human In Use Test of GINHI-HP-009 in Healthy Adults

Role: lead

NCT07533474Not ApplicableCompleted

Human In Use Test of GINPI-HP-004 in Healthy Adults

Role: lead

NCT07448129Not ApplicableNot Yet Recruiting

Clinical Trial to Evaluate the Efficacy and Safety of SUBMO® as a Submucosal Injection Agent in Endoscopic Resection of Superficial Gastrointestinal Lesions.

Role: lead

NCT07441135Not ApplicableNot Yet Recruiting

Efficacy and Safety of BtH Body 2.2% (Injectable Hyaluronic Acid) in Volumizing and Contouring Large Areas of the Body: Prospective Clinical Investigation.

Role: lead

NCT07406152Not ApplicableRecruiting

Efficacy and Safety of ZKARE® Gel and Its Accessory ZKAPI® in the Treatment of Chronic Ulcers.

Role: lead

NCT07343973Not ApplicableCompleted

Post-Market Study on the Safety and Effectiveness of the OpHLINE OVD in Cataract Surgery

Role: lead

NCT07402395Not ApplicableCompleted

Clinical Study on the Safety and Efficacy of an Injectable Hyaluronic Acid for Improving the Aesthetic Rejuvenation of the Vulvovaginal Area

Role: lead

NCT07301658Not ApplicableCompleted

Efficacy and Safety of Revodiol Calming Cream® in Atopic Dermatitis.

Role: lead

NCT07301619Not ApplicableCompleted

Post-market Study on BtHCROSS® for Restoring Facial Volume After a Single Injection

Role: lead

NCT06975631Not ApplicableCompleted

Post-market Study on TrHCROSS® in Knee Osteoarthritis After a Single Injection

Role: lead

NCT06741280Not ApplicableCompleted

Post-marketing Study for the Evaluation of Profilm Mouth Sores

Role: lead

NCT06732830Not ApplicableCompleted

Clinical Trial to Assess the Effectiveness of I+Med's DayDrop Advanced Ophthalmic Drop

Role: lead

NCT06734728Not ApplicableCompleted

Post-marketing Study for the Evaluation of Profilm Cold Sores

Role: lead

NCT06731725Not ApplicableCompleted

Post-marketing Study Focused on Evaluating I+Med's DayDrop for Improving Signs and Symptoms of Mild/Moderate Dry Eye

Role: lead

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