Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

3.3%

1 terminated/withdrawn out of 30 trials

Success Rate

96.7%

+10.2% vs industry average

Late-Stage Pipeline

43%

13 trials in Phase 3/4

Results Transparency

31%

9 of 29 completed trials have results

Key Signals

9 with results

Enrollment Performance

Analytics

Phase 1
15(50.0%)
Phase 3
13(43.3%)
Phase 2
2(6.7%)
30Total
Phase 1(15)
Phase 3(13)
Phase 2(2)

Activity Timeline

Global Presence

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Clinical Trials (30)

Showing 20 of 30 trials
NCT00961350Phase 3Completed

A Study to Evaluate the Incidence of Gastric Ulcers Following Administration of Either PA32540 or Enteric Coated Aspirin 325 mg in Subjects Who Are at Risk for Developing Aspirin-Associated Ulcers

Role: lead

NCT00960869Phase 3Completed

Study to Evaluate the Incidence of Gastric Ulcers Following Administration of Either PA32540 or Enteric Coated Aspirin 325 mg in Subjects Who Are at Risk for Developing Aspirin-Associated Ulcers

Role: lead

NCT00995410Phase 3Completed

Study to Evaluate the Long-Term Safety of PA32540 in Subjects Who Are at Risk for Developing Aspirin-Associated Gastric Ulcers

Role: lead

NCT00596245Phase 1Completed

Open-Label, Placebo-Controlled, Parallel Group Study in Healthy Volunteers to Evaluate the Effects of Two Single MT 400 or Naproxen Sodium Tablets

Role: collaborator

NCT00293657Phase 2Completed

Study of Lornoxicam or Placebo for Acute Treatment of the Headache of Migraine.

Role: lead

NCT00293631Phase 2Completed

Study of Lornoxicam or Ketorolac or Placebo for Post-Operative Pain After Bunionectomy

Role: lead

NCT01557335Phase 1Completed

A Study to Evaluate Platlet Aggregation of Clopidogrel, EC Aspirin 81 mg, EC Omeprazole 40 mg Compare to PA32540

Role: lead

NCT00664560Phase 3Completed

Efficacy Study of PN400 (VIMOVO) Twice Daily and Celebrex Once Daily in Patients With Osteoarthritis

Role: lead

NCT00665431Phase 3Completed

Efficacy Study of PN400 (VIMOVO) Twice Daily and Celebrex Once Daily in Patients With Osteoarthritis

Role: lead

NCT00527787Phase 3Completed

Evaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers Compared to Non-steroidal Antiinflammatory Drug (NSAID) Naproxen

Role: lead

NCT01129011Phase 3Completed

Evaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers Compared to Non-steroidal Antiinflammatory Drug (NSAID) Naproxen

Role: lead

NCT01094483Phase 1Completed

A Study Assessing Inhibition of Serum Thromboxane B2 Levels With PN400 and Low Dose Aspirin

Role: collaborator

NCT00594854Phase 3Terminated

Evaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers in High Risk Subjects Compared to Arthrotec

Role: lead

NCT00527904Phase 3Completed

A 12-month, Phase 3, Open-label, Multi-center Study to Evaluate the Long-term Safety of PN400 (VIMOVO)

Role: lead

NCT00992381Phase 1Completed

Comparison Study of a New Combination of 2 Marketed Medications (Esomeprazole and Naprosyn) Versus Naprosyn Alone

Role: collaborator

NCT00729495Phase 1Completed

Phase I Study to Evaluate Bioavailability of Overencapsulated Celecoxib

Role: lead

NCT00441519Phase 1Completed

A Parallel Group Study to Compare the Gastroprotective Effects of PA 325 Versus 81 mg Enteric Coated Aspirin

Role: lead

NCT00700687Phase 1Completed

Study Evaluating the Effect on Gastroduodenal Mucosa of PA32540, PA32540 and Celecoxib, and Aspirin With Celecoxib

Role: lead

NCT00749385Phase 1Completed

A Pharmacokinetic (PK) Study Evaluating Naproxen and Esomeprazole Plasma Levels

Role: lead

NCT00676442Phase 1Completed

Study Evaluating the Effect of Food on the Bioavailability of PN400 Components

Role: lead