Registry-listed formulations

This catalogue entry has no confirmed scientific concept.

Each study is counted once in the molecule profile. Registry products remain separate. Naming an ingredient does not establish that products are interchangeable or what participants received.

0 source entries across 0 studies. This list may not include all unresolved or historical entries.

    Success Metrics

    Clinical Success Rate
    100.0%

    Based on 14 completed trials

    Completion Rate
    100%(14/14)
    Active Trials
    0(0%)
    Results Posted
    0%(0 trials)

    Phase Distribution

    Phase 2
    4
    29%
    Phase 3
    8
    57%
    Phase 1
    2
    14%

    Phase Distribution

    2

    Early Stage

    4

    Mid Stage

    8

    Late Stage

    Phase Distribution14 total trials
    Phase 1Safety & dosage
    2(14.3%)
    Phase 2Efficacy & side effects
    4(28.6%)
    Phase 3Large-scale testing
    8(57.1%)

    Highest Phase Reached

    Phase 3

    Trial Status & Enrollment

    Completion Rate

    100.0%

    14 of 14 finished

    Non-Completion Rate

    0.0%

    0 ended early

    Currently Active

    0

    trials recruiting

    Total Trials

    14

    all time

    Status Distribution
    Completed(14)

    Detailed Status

    Completed14

    Development Timeline

    Analytics

    Development Status

    Total Trials
    14
    Active
    0
    Success Rate
    100.0%
    Most Advanced
    Phase 3

    Trials by Phase

    Phase 12 (14.3%)
    Phase 24 (28.6%)
    Phase 38 (57.1%)

    Trials by Status

    completed14100%

    Recent Activity

    Clinical Trials (14)

    Showing 14 of 14 trials
    NCT00192192Phase 3

    Trial to Investigate Immune Responses Elicited by a Liquid Formulation of Influenza Virus Vaccine, Trivalent, Types A & B, Live Cold Adapted (CAIV-T) in Healthy Adults

    Completed
    NCT00192231Phase 3

    Trial to Investigate Immune Responses Elicited by a Liquid Formulation of Influenza Virus Vaccine,(CAIV-T)

    Completed
    NCT00192348Phase 1

    A Prospective, Randomized, Double-Blind, Placebo-Controlled Trial to Assess the Safety and Tolerability of Influenza Virus Vaccine,(CAIV-T) in Healthy Infants

    Completed
    NCT00192270Phase 2

    Trial to Assess Safety, Tolerability, and Immunogenicity of Influenza Virus Vaccine, Trivalent, Types A and B, Live Cold-adapted (CAIV-T) in Healthy Children

    Completed
    NCT00192309Phase 2

    Phase II Study to Investigate the Kinetics of the Immune Response Generated by Influenza Virus Vaccine.

    Completed
    NCT00224783Phase 1

    Phase I Trial Evaluating Safety and Tolerability of CAIV-T in Healthy Japanese Male Adults

    Completed
    NCT00192283Phase 3

    Trial to Determine the Safety and Efficacy of Influenza Virus Vaccine, Trivalent, Types A & B, Live Cold- Adapted (CAIV-T) in Healthy Children Attending Day Care Centers

    Completed
    NCT00192166Phase 2

    Trial to Assess Safety, Efficacy, Tolerability and Immunogenicity of Influenza Virus Vaccine, Liquid Formulation (CAIV-T), Administered Concomitantly With a Combination Live, Attenuated, Mumps, Measles, and Rubella Vaccine in Healthy Children Aged 11 - 24 Months

    Completed
    NCT00111579Phase 2

    Study to Evaluate the Immune Responses of Trivalent Cold-Adapted Influenza Vaccine (CAIV-T) Compared With (TIV)

    Completed
    NCT00192335Phase 3

    Trial to Demonstrate Equivalent Immunogenicity of CAIV-T and FLUMIST in Healthy Participants

    Completed
    NCT00192361Phase 3

    Trial of the Safety, Transmissibility, and Phenotypic and Genotypic Stability of Influenza Virus Vaccine,(CAIV-T), in Children Who Attend Day Care. (Final Report Version 2.0)

    Completed
    NCT00192400Phase 3

    Trial to Assess the Safety and Tolerability of the Liquid Formulation of CAIV-T in Healthy Children.

    Completed
    NCT00192426Phase 3

    Trial to Evaluate the Immune Response to OPV When Administered Concomitantly With CAIV-T to Healthy Children.

    Completed
    NCT00217230Phase 3

    Trial To Assess Safety And Efficacy Of Influenza Virus Vaccine, Trivalent, Types A & B, Live Cold-Adapted (CAIV-T) In Adults Aged 60 Years And Older

    Completed

    All 14 trials loaded

    Drug Details

    Intervention Type
    Biological
    Total Trials
    14