Success Metrics

Clinical Success Rate
100.0%

Based on 7 completed trials

Completion Rate
100%(7/7)
Active Trials
7(41%)
Results Posted
57%(4 trials)

Phase Distribution

Ph phase_3
5
29%
Ph early_phase_1
1
6%
Ph phase_4
1
6%
Ph phase_1
2
12%
Ph phase_2
1
6%

Phase Distribution

3

Early Stage

1

Mid Stage

6

Late Stage

Phase Distribution10 total trials
Early Phase 1First-in-human
1(10.0%)
Phase 1Safety & dosage
2(20.0%)
Phase 2Efficacy & side effects
1(10.0%)
Phase 3Large-scale testing
5(50.0%)
Phase 4Post-market surveillance
1(10.0%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

100.0%

7 of 7 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

7

trials recruiting

Total Trials

17

all time

Status Distribution
Active(10)
Completed(7)

Detailed Status

Completed7
Recruiting6
Not yet recruiting3
Active, not recruiting1

Development Timeline

Analytics

Development Status

Total Trials
17
Active
7
Success Rate
100.0%
Most Advanced
Phase 4

Trials by Phase

Early Phase 11 (10.0%)
Phase 12 (20.0%)
Phase 21 (10.0%)
Phase 35 (50.0%)
Phase 41 (10.0%)

Trials by Status

recruiting635%
active_not_recruiting16%
completed741%
not_yet_recruiting318%

Recent Activity

Clinical Trials (17)

Showing 17 of 17 trials
NCT06042049Phase 3

A Study to Assess Safety, Pharmacokinetics Anti-Drug Antibody and Anti-RSV Antibody After 2 Doses of Nirsevimab

Completed
NCT05110261Phase 3

Evaluate the Safety and Efficacy of Nirsevimab in Healthy Preterm and Term Infants in China

Completed
NCT07109297Phase 4

Study of Monoclonal Antibody Nirsevimab Against Respiratory Syncytial Virus (RSV) in Participants up to 24 Months of Age in India

Active Not Recruiting
NCT07382219

Real-World Effectiveness of Nirsevimab Against RSV-Related and All-Cause Respiratory Tract Infections in Chinese Infants

Completed
NCT07363837Phase 1

Phase Ib/IIa Clinical Trial of SIBP-A16 Injection in Premature Infants and Full-term Infants

Not Yet Recruiting
NCT07200206

A Post-marketing Surveillance Study of Beyfortus (Nirsevimab) in Republic of Korea

Recruiting
NCT07106918Early Phase 1

A Clinical Trial of SIBP-A16 Injection in Healthy Adults

Recruiting
NCT07232706Phase 3

Prevention of RSV Infection in Infants by Administering Nirsevimab to Infants, With or Without Maternal RSV Vaccination

Not Yet Recruiting
NCT06325332

BEYFORTUS™ (Nirsevimab) Effectiveness Against Medically-Attended RSV Events in Infants (BEAR Study)

Completed
NCT05437510Phase 3

Study of a Single Intramuscular Dose of Nirsevimab in the Prevention of Hospitalizations Due to Respiratory Syncytial Virus (RSV) Infection in Healthy Term and Preterm Infants During the First Year of Life

Completed
NCT06172660

Real-World Effectiveness of Perinatal RSV Immunoprophylaxis

Recruiting
NCT07041190Phase 3

Pregnancy and Infant PrEparedness pLatform IN Europe, RSV-International Adaptive Platform Trial to Evaluate Two Approved Prevention Options to Prevent Respiratory Syncytial Virus in Infants: Maternal Vaccine to Women in Pregnancy and Monoclonal Antibody to the Infants, Given Alone or in Combination.

Not Yet Recruiting
NCT06856967

Evaluation of the Effect of Nirsevimab on Hospitalizations Due to RSV Infection in Infants Under One Year of Age.

Recruiting
NCT06511687

Effectiveness And Impact Of Nirsevimab In Chile (NIRSE-CL)

Recruiting
NCT06180993

Evaluation of the Effectiveness and Impact of Nirsevimab Administered as Routine Immunization

Recruiting
NCT04484935Phase 2

Evaluate the Safety and Tolerability, for Nirsevimab in Immunocompromised Children

Completed
NCT04840849Phase 1

Evaluate the Pharmacokinetics, Safety, and Tolerability of Nirsevimab in Healthy Chinese Adults

Completed

All 17 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
17