Success Metrics

Clinical Success Rate
92.3%

Based on 24 completed trials

Completion Rate
92%(24/26)
Active Trials
1(4%)
Results Posted
38%(9 trials)
Terminated
2(7%)

Phase Distribution

Ph phase_1
5
19%
Ph phase_3
1
4%
Ph phase_2
5
19%
Ph early_phase_1
1
4%
Ph phase_4
9
33%
Ph not_applicable
3
11%

Phase Distribution

6

Early Stage

5

Mid Stage

10

Late Stage

Phase Distribution24 total trials
Early Phase 1First-in-human
1(4.2%)
Phase 1Safety & dosage
5(20.8%)
Phase 2Efficacy & side effects
5(20.8%)
Phase 3Large-scale testing
1(4.2%)
Phase 4Post-market surveillance
9(37.5%)
N/ANon-phased studies
3(12.5%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

92.3%

24 of 26 finished

Non-Completion Rate

7.7%

2 ended early

Currently Active

1

trials recruiting

Total Trials

27

all time

Status Distribution
Active(1)
Completed(24)
Terminated(2)

Detailed Status

Completed24
Terminated2
Active, not recruiting1

Development Timeline

Analytics

Development Status

Total Trials
27
Active
1
Success Rate
92.3%
Most Advanced
Phase 4

Trials by Phase

Early Phase 11 (4.2%)
Phase 15 (20.8%)
Phase 25 (20.8%)
Phase 31 (4.2%)
Phase 49 (37.5%)
N/A3 (12.5%)

Trials by Status

active_not_recruiting14%
completed2489%
terminated27%

Recent Activity

Clinical Trials (27)

Showing 20 of 27 trialsScroll for more
NCT02518555Phase 2

Ibrutinib as an Immune Modulating Agent for Patients With Asymptomatic, High-risk CLL/SLL Risk Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Active Not Recruiting
NCT04080531Phase 4

Influenza Vaccination for Flu Prevention in Patients With Plasma Cell Disorders

Completed
NCT03179761Phase 2

High vs. Standard Dose Flu Vaccine in Adult Stem Cell Transplant Recipients

Completed
NCT02860039Phase 2

High Dose Flu Vaccine in Treating Children Who Have Undergone Donor Stem Cell Transplant

Completed
NCT06252051Phase 4

Effectiveness of Trivalent Influenza Vaccine (TIV) in Type 2 Diabetes Mellitus (T2DM) Patients With and Without Complications of Chronic Kidney Disease (CKD)

Completed
NCT04484532Early Phase 1

Evaluation of Antibody Response to High-Dose Seasonal Influenza Vaccination in Patients With Myeloid Malignancy Receiving Chemotherapy and Healthy Volunteers

Completed
NCT02882100Phase 4

Adjuvanted Influenza Vaccination in U.S. Nursing Homes

Completed
NCT02747407

Qualitative, Qualitative, and Functional Studies Over the First Year in Measuring Immune System Response During the First Year of Therapy in Patients With Brain Tumors

Completed
NCT01561989Not Applicable

Cholecalciferol and Flu Vaccine in Treating Healthy Participants

Terminated
NCT03336593Phase 2

Protectivity and Safety of Quadrivalent Influenza HA Vaccine in Indonesian Population

Completed
NCT01695733Phase 1

Response to Influenza Vaccine in Patients With Non-Hematologic Malignancies Receiving Chemotherapy

Terminated
NCT01306669Phase 3

Influenza Vaccine Trial in HIV Uninfected Pregnant Women

Completed
NCT01941758Phase 1

High-Dose Trivalent Influenza Vaccine in Inducing Immune Response Patients With Central Nervous System Tumors

Completed
NCT01474174

Trivalent Influenza Vaccine in Preventing Flu in Patients With Central Nervous System Tumors

Completed
NCT01863433Phase 4

A Study to Assess the Immunogenicity and Safety of a Trivalent Influenza Vaccine Containing the 2013/2014 Formulation of Enzira® Vaccine in Healthy Volunteers

Completed
NCT00964821

Flu Vaccine in Preventing Influenza Infection in Healthy Volunteers and in Patients Who Have Undergone Stem Cell Transplant

Completed
NCT01264601Not Applicable

Safe Administration of Flu Vaccine to Egg Allergic Children

Completed
NCT01246999Phase 4

Effect of Age and Prior Immunity to Response to Seasonal Influenza Vaccines in Children

Completed
NCT02473510Phase 4

Study to Evaluate the Safety of 3 New 6:2 Influenza Virus Reassortants in Adults for the 2015-2016 Season

Completed
NCT00848848Phase 1

Safety, Tolerability, and Immunogenicity of Different Combinations of Trivalent Influenza Vaccine Varying Influenza Antigen Dose, Adjuvant Dose, and Route of Administration in Healthy Elderly Individuals Ages 65 Years and Older

Completed

Drug Details

Intervention Type
BIOLOGICAL
Total Trials
27