Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 50/100

Failure Rate

13.6%

3 terminated/withdrawn out of 22 trials

Success Rate

86.4%

-0.1% vs industry average

Late-Stage Pipeline

18%

4 trials in Phase 3/4

Results Transparency

16%

3 of 19 completed trials have results

Key Signals

3 with results

Enrollment Performance

Analytics

Phase 2
10(45.5%)
N/A
6(27.3%)
Phase 3
4(18.2%)
Phase 1
2(9.1%)
22Total
Phase 2(10)
N/A(6)
Phase 3(4)
Phase 1(2)

Activity Timeline

Global Presence

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Clinical Trials (22)

Showing 20 of 22 trials
NCT00318903Phase 2Completed

Irinotecan and Taxotere With Radiotherapy as Preoperative Treatment in Resectable Esophageal Cancer

Role: collaborator

NCT00193050Phase 2Completed

Weekly Gemcitabine, Epirubicin, and Docetaxel in Locally Advanced or Inflammatory Breast Cancer

Role: collaborator

NCT00003748Phase 2Completed

Irinotecan in Treating Patients With Esophageal or Stomach Cancer

Role: collaborator

NCT00201747Phase 2Completed

Sequentially Administered CPT-11 and Mitomycin C in Patients With Advanced Esophageal and Stomach Cancer

Role: collaborator

NCT00193375Phase 2Completed

Irinotecan, Carboplatin and Radiation Therapy Followed by Bevacizumab in Limited Stage Small Cell Lung Cancer

Role: collaborator

NCT00193596Phase 3Completed

Gemcitabine/Irinotecan/ZD1839 vs Paclitaxel/Carboplatin/Etoposide/ZD1839 in Carcinoma of Unknown Primary Site

Role: collaborator

NCT01422317Phase 3Completed

Effects of High-dose n-3 Fatty Acids on Clinical Outcome and Serum Lipids - Omacor Following Acute Myocardial Infarction

Role: collaborator

NCT00193024Phase 2Terminated

Epirubicin and Docetaxel in the Treatment of Patients With Metastatic Breast Cancer

Role: collaborator

NCT00177853Phase 1Terminated

Celecoxib, Irinotecan and Concurrent Radiotherapy in Preoperative Pancreatic Cancer

Role: collaborator

NCT00193349Phase 2Completed

Gleevec Combined With Camptosar Plus Paraplatin in Previously Untreated Extensive Stage Small Cell Lung Cancer

Role: collaborator

NCT00002420Phase 2Terminated

The Safety and Effectiveness of Didanosine Plus Stavudine Plus Delavirdine Mesylate Plus MKC-442 in HIV-Infected Patients Who Have Not Had Success With Protease Inhibitors

Role: collaborator

NCT00002312Not ApplicableCompleted

The Safety and Effectiveness of U-90152 in HIV-1 Infected Patients Who Take Zidovudine

Role: lead

NCT00002236Not ApplicableCompleted

A Study to Find the Best Dosing Schedule for Delavirdine, Zidovudine, and Indinavir in HIV-Positive Patients

Role: lead

NCT00002211Not ApplicableCompleted

Safety and Effectiveness of Giving Combinations of Three or Four Anti-HIV Drugs to HIV-Infected Patients

Role: lead

NCT00002124Phase 3Completed

A Double-Blind, Randomized, Dose Response Study of Three Doses of Delavirdine Mesylate (U-90152S) in Combination With Zidovudine (ZDV) Versus ZDV Alone in HIV-1 Infected Individuals With CD4 Counts of 200-500mm3

Role: lead

NCT00002094Not ApplicableCompleted

Prospective Open-Label Study of the Emergence of Drug Resistance in Patients Infected With HIV-1 Who Are Taking Oral U-87201E

Role: lead

NCT00002210Phase 2Completed

A Study of Delavirdine Mesylate in Combination With Other Anti-HIV Drugs in HIV-Infected Children and Babies

Role: lead

NCT00002401Not ApplicableCompleted

A Study of Delavirdine Used Together With Other Anti-HIV Drugs in HIV-Infected Patients

Role: lead

NCT00002322Phase 2Completed

A Study of Different Doses of Atevirdine Mesylate Plus Zidovudine in HIV-Positive Patients

Role: lead

NCT00002087Phase 1Completed

Safety, Tolerance, Efficacy and Pharmacokinetics of Multiple Doses of sCD4-PE40 in the Treatment of HIV-Infected Individuals

Role: lead