Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 50/100

Failure Rate

8.2%

8 terminated/withdrawn out of 98 trials

Success Rate

83.7%

-2.9% vs industry average

Late-Stage Pipeline

27%

26 trials in Phase 3/4

Results Transparency

15%

6 of 41 completed trials have results

Key Signals

17 recruiting6 with results5 withdrawn

Enrollment reporting

Analytics

N/A
29(34.9%)
Phase 4
16(19.3%)
Phase 2
13(15.7%)
Phase 3
10(12.0%)
Phase 1
7(8.4%)
Phase 1/2
3(3.6%)
Early Phase 1
3(3.6%)
Phase 2/3
2(2.4%)
83Total
N/A(29)
Phase 4(16)
Phase 2(13)
Phase 3(10)
+4 more

Activity Timeline

Global Presence

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Clinical Trials (98)

Showing 20 of 98 trials
NCT07875504Not ApplicableNot Yet Recruiting

A Clinical Trial of Analytical Treatment Interruption in People With HIV With a Highly Favourable Profile

Role: lead

NCT04304014Not ApplicableCompleted

Assessment of the Impact of Type of Probiotic, Delivery Type and Feeding Type on Baby's Microbiota After Dysbiotic Delivery

Role: lead

NCT07813377Recruiting

Usefulness of Thromboelastography as a Predictor of Prognosis in Patients Undergoing Surgery for Glial Tumors and of the Risk of Postoperative Thromboembolic Disease (GliTEM)

Role: lead

NCT07702695Not ApplicableNot Yet Recruiting

A Mediterranean Diet-Based Culinary Intervention in Adults With Metabolic Syndrome

Role: lead

NCT07696793Phase 4Recruiting

Efficacy and Tolerability of a Simethicone-containing Evacuating Solution for Colorectal Cancer Screening Colonoscopy

Role: lead

NCT04487756Phase 1/2Completed

Combination of Atezolizumab With Dendritic Cell Vaccine in Patients With Lung Cancer

Role: collaborator

NCT07018947Phase 2Recruiting

Study to Evaluate the Efficacy and Safety of Atezolizumab and Bevacizumab as Neoadjuvant Plus Adjuvant Treatment in HCC

Role: lead

NCT05398679Phase 4Recruiting

Oral Antimicrobial Treatment vs. Outpatient Parenteral for Infective Endocarditis

Role: lead

NCT07163403Phase 1Recruiting

First in Human Pilot Study to Assess the Safety and Efficacy of Dendritic Cells Loaded With Frameshift Derived Neopeptides for the Prevention of Cancer in of Lynch Syndrome Carriers

Role: lead

NCT07454096Phase 4Not Yet Recruiting

Application of Radiomics for Diagnosis and Follow-up of Cardiovascular Device Infections: PREDICT Study

Role: lead

NCT07454122Phase 1Not Yet Recruiting

CD5CAR-NK Cells for Refractory Invasive Mold Disease

Role: lead

NCT07412873Phase 4Not Yet Recruiting

Study on Sexual Health and Self-perceived Quality of Life (PROMs) in Patients Treated for Cervical Cancer

Role: lead

NCT05937620Not ApplicableRecruiting

Sentinel Node Detection With Technetium-99m Albumin Nanocolloid and ICG in Patients With Epithelial Ovarian Cancer

Role: lead

NCT07394101Not ApplicableNot Yet Recruiting

Pharmacokinetic Characterization of Tartaric Acid in Humans

Role: lead

NCT07169643Phase 3Recruiting

Darbepoetin in Patients Candidates for Liver Transplant. (EPO-LT Trial)

Role: lead

NCT07270874Phase 4Not Yet Recruiting

Study to Evaluate the Efficacy of Intravenous Administration of Human Albumin Versus Saline Solution in Patients With descompénsate Cirrhosis Grade 1B or Higher Renal Failure

Role: lead

NCT03360682Phase 4Completed

Clinical Trial to Evaluate the Efficacy, Pharmacokinetics (PK) Interactions and Safety of Dolutegravir Plus 2 Nucleoside Reverse Transcriptase Inhibitors (NRTIs) in HIV-1-Infected Solid Organ Transplant Patients

Role: lead

NCT02558933Not ApplicableCompleted

Epigallocatechin Gallate (EGCG) to Improve Cognitive Performance in Foetal Alcohol Syndrome (FAS) Children

Role: lead

NCT07105384Phase 2Active Not Recruiting

Quantification Tools for a Novel Tau PET Marker in a Rare Neurological Disease: 18F-PI-2620 in Progressive Supranuclear Palsy

Role: lead

NCT03311945Phase 3Completed

Simplification Study of HIV-1 Infected Patients With Virological Suppression Under the Combination of Lamivudine (150 mg BID) Plus Raltegravir (400 mg BID) Switching to Lamivudine (300 mg QD) Plus Raltegravir (1200 mg QD) : Roll-over Study of the RALAM

Role: collaborator