Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

0.0%

0 terminated/withdrawn out of 17 trials

Success Rate

100.0%

+13.5% vs industry average

Late-Stage Pipeline

35%

6 trials in Phase 3/4

Results Transparency

0%

0 of 15 completed trials have results

Key Signals

Enrollment Performance

Analytics

Phase 1
6(35.3%)
Phase 3
6(35.3%)
Phase 2
5(29.4%)
17Total
Phase 1(6)
Phase 3(6)
Phase 2(5)

Activity Timeline

Global Presence

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Clinical Trials (17)

Showing 17 of 17 trials
NCT05739474Phase 3Unknown

Tolerability, Safety and Immunogenicity Trial of the Flu-M Tetra Vaccine in Children

Role: lead

NCT05156723Phase 1Completed

Study of the Immunogenicity, Safety and Tolerability of the Convacell Vaccine.

Role: lead

NCT05726084Phase 2Unknown

Immunogenicity, Efficacy and Safety Trial of the Convacell Vaccine in Healthy Volunteers Aged 18 Years and Older

Role: lead

NCT05869201Phase 2Completed

Tolerability, Safety and Immunogenicity Trial of the Flu-M Quadro, Tetravalent Inactivated Split Influenza Vaccine

Role: lead

NCT05308212Phase 2Completed

Tolerability, Safety and Immunogenicity Trial of the FLU-M® Tetra

Role: lead

NCT05470582Phase 3Completed

Trial of Tolerability, Safety and Immunogenicity of the Flu-M Vaccine in Children Between 6 Months and 9 Years Old

Role: lead

NCT05457894Phase 3Completed

Trial of Tolerability, Reactogenicity, Safety and Immunogenicity of Flu-M [Inactivated Split Influenza Vaccine] in Pregnant Women

Role: lead

NCT05401305Phase 1Completed

Safety and Reactogenicity Trial of Vaccine for the Prevention of Infections Caused by Haemophilus Influenzae Type b

Role: lead

NCT05398562Phase 1Completed

Tolerability and Reactogenicity Trial of the Recombinant Tuberculosis Allergen in Healthy Volunteers

Role: lead

NCT05317767Phase 3Completed

The Objectives of This Study Are Comparative Assessment of the Tolerability, Safety and Immunogenicity of the Flu-M Vaccine vs. the Ultrix® Vaccine by Single Vaccination of Children Aged 6 to 17 Years.

Role: lead

NCT05312294Phase 3Completed

Tolerability, Safety and Immunogenicity Trial of the Flu-M® Inactivated Vaccine in Volunteers Aged 18 to 60 Years

Role: lead

NCT05297994Phase 2Completed

Trial of the Reactogenicity, Safety and Immunogenicity of the Flu-M Vaccine Manufactured by FSUE SPbSRIVS FMBA

Role: lead

NCT05208996Phase 1Completed

The siCoV/KK46 Drug Open-safety Study

Role: collaborator

NCT05184127Phase 2Completed

Evaluation of Safety & Efficacy of MIR 19 ® Inhalation Solution in Patients With Moderate COVID-19

Role: collaborator

NCT05126979Phase 1Completed

The Objectives of This Study Are Study of the Reactogenicity, Safety and Immunogenicity of Flu-M Inactivated Split Influenza Vaccine in Volunteers Aged 18-60 Years

Role: lead

NCT05089123Phase 3Completed

The Objectives of This Study Are Study the Immunogenicity and Safety of the Flu-M [Inactivated Split Influenza Vaccine], vs. the Ultrix® Inactivated Split Influenza Vaccine, in Volunteers Who Are Over 60 Years Old

Role: lead

NCT05152017Phase 1Completed

The Objectives of This Study Are Study the Safety, Reactogenicity and Obtain Preliminary Data on the Immunogenicity of Flu-M Quadro, 4-valent Inactivated Split Influenza Vaccine, in Healthy Volunteers

Role: lead

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