deltatrials
Recruiting PHASE2/PHASE3 INTERVENTIONAL 2-arm NCT05491525

A Study of Vibegron in Pediatric Participants 2 Years to Less Than (<) 18 Years of Age With NDO and on CIC (KANGUROO)

A Phase 2/3, Open-label, Baseline-controlled, Multicenter, Long-term Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Vibegron in Pediatric Subjects 2 Years to < 18 Years of Age With Neurogenic Detrusor Overactivity (NDO) on Clean Intermittent Catheterization (CIC)

Sponsor: Urovant Sciences GmbH

Interventions Vibegron
Updated 5 times since 2022 Last updated: Jul 2, 2024 Started: Oct 12, 2022 Primary completion: Jan 31, 2027 Completion: Sep 30, 2027
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE2/PHASE3 clinical study on Neurogenic Detrusor Overactivity, this trial is actively recruiting participants. The trial is conducted by Urovant Sciences GmbH and has accumulated 5 data snapshots since 2022. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~Sep 2022 – ~Jul 2023 · 10 months · monthly snapshotNot Yet Recruiting~Jul 2023 – ~Jul 2024 · 12 months · monthly snapshotRecruiting~Jul 2024 – ~Aug 2024 · 31 days · monthly snapshotRecruiting~Aug 2024 – ~Sep 2024 · 31 days · monthly snapshotRecruiting~Sep 2024 – present · 21 months · monthly snapshotRecruiting

Change History

5 versions recorded
  1. Sep 2024 — Present [monthly]

    Recruiting PHASE2/PHASE3

  2. Aug 2024 — Sep 2024 [monthly]

    Recruiting PHASE2/PHASE3

  3. Jul 2024 — Aug 2024 [monthly]

    Recruiting PHASE2/PHASE3

    Phase: PHASE2_PHASE3PHASE2/PHASE3

  4. Jul 2023 — Jul 2024 [monthly]

    Recruiting PHASE2_PHASE3

    Status: Not Yet RecruitingRecruiting

  5. Sep 2022 — Jul 2023 [monthly]

    Not Yet Recruiting PHASE2_PHASE3

    First recorded

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Urovant Sciences GmbH
Data source: Urovant Sciences GmbH

For direct contact, visit the study record on ClinicalTrials.gov .