Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

0.7%

1 terminated/withdrawn out of 142 trials

Success Rate

99.0%

+12.5% vs industry average

Late-Stage Pipeline

32%

45 trials in Phase 3/4

Results Transparency

4%

4 of 96 completed trials have results

Key Signals

6 recruiting4 with results

Enrollment Performance

Analytics

Phase 1
70(52.2%)
Phase 4
24(17.9%)
Phase 3
21(15.7%)
Phase 2
14(10.4%)
N/A
5(3.7%)
134Total
Phase 1(70)
Phase 4(24)
Phase 3(21)
Phase 2(14)
+1 more

Activity Timeline

Global Presence

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Clinical Trials (142)

Showing 20 of 142 trials
NCT07297940Phase 1Completed

Pharmacokinetics and Safety Profiles of DA-1229_01 in Healthy Subjects at Fasting State

Role: lead

NCT07481357Phase 1Not Yet Recruiting

A First-In-Human Phase I/IIa Study to Evaluate DA 3501 in Patients With Advanced Gastric or Gastro-esophageal Junction Adenocarcinoma and Pancreatic Ductal Adenocarcinoma

Role: lead

NCT06654856Completed

The Effectiveness and Safety of Dong-A Opalmon® Tablet in Patients With Acquired Lumbar Spinal Stenosis

Role: lead

NCT07342062Phase 1Not Yet Recruiting

Pharmacokinetics and Safety Profiles of DA-1229_01 in Healthy Subjects at Fed State

Role: lead

NCT05845489Phase 4Recruiting

Harmonizing Optimal Strategy for Treatment of Coronary Artery Stenosis- CloPidogREl for Primary preVENTION (HOST-PREVENTION)

Role: collaborator

NCT07239440Phase 2Not Yet Recruiting

Clinical Trial to Evaluate the Efficacy and Safety of DA-2811 When Added to Ongoing BT-1 and BT-2 Combination Therapy in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control

Role: lead

NCT07239453Phase 1Enrolling By Invitation

Clinical Trial of Comparing DA-2902 and DA-2902-R in Healthy Adult Subjects

Role: lead

NCT06290349Phase 3Active Not Recruiting

Efficacy and Safety of DA5221-T When Added to Ongoing DA5221-B1 and DA5221-B2 Combination Therapy in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control

Role: lead

NCT07046715Phase 1Completed

Clinical Trial Comparing Single-administration of DA-5222 and Co-administration of DA-5222-R1, DA-5222-R2 and DA-5222-R3 in Healthy Adult Subjects in Fed State

Role: lead

NCT07229534Phase 4Not Yet Recruiting

Clinical Trial to Evaluate the Efficacy and Safety of DA-5218 in Patients With Type 2 Diabetes

Role: lead

NCT07139886Phase 2Completed

A Study to Evaluate the Safety and Efficacy of DA9601 for Acute and Chronic Gastritis and to Determine the Optimal Clinical Dosage and Administration

Role: lead

NCT06151210Phase 3Completed

Clinical Trial to Evaluate the Efficacy and Safety of DA-5219 in Patients With Acute or Chronic Gastritis

Role: lead

NCT05630768Phase 4Completed

Efficacy and Safety of Actonel® After Denosumab Discontinuation in Postmenopausal Osteoporosis Women

Role: lead

NCT07027982Phase 1Completed

A Study to Evaluate the Pharmacokinetics and Safety of Diluted vs. Undiluted Intravenous DA-5217 in Healthy Adult Subjects

Role: lead

NCT07007520Phase 1Recruiting

A Study to Evaluate the Food Effect on the Pharmacokinetics of DA-5223 in Healthy Adult Subjects

Role: lead

NCT07007533Phase 1Completed

A Study to Compare and Evaluate the Safety, Tolerability and Pharmacokinetics Between DA-5223 and DA-5223-R in Healthy Adult Subjects

Role: lead

NCT07096921Not ApplicableActive Not Recruiting

The Effect of Two Prokinetics in Patients With Functional Dyspepsia

Role: collaborator

NCT06993181Phase 1Not Yet Recruiting

Clinical Trial of Comparing DA-5222 Single-administration and Co-administration of DA-5222-R1, DA-5222-R2 and DA-5222-R3 in Healthy Adult Subjects

Role: lead

NCT06993168Phase 1Not Yet Recruiting

To Evaluate Effect of Food of DA-5222 in Healthy Adult Subjects

Role: lead

NCT06627322Not ApplicableRecruiting

A Registry-based Randomized Controlled Trial in Type 2 Diabetes With Cardiovascular Risk Factors (REMATCH)

Role: collaborator