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Effects of Pazopanib on Hereditary Hemorrhagic Telangiectasia Related Epistaxis and Anemia (Paz)

Study acronym: Paz
StatusActive, Not Recruiting
PhasePhase 2/3
SponsorCure HHT
Started
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Record History

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  1. Minor Primary completion date changed from estimate of Nov 2025 to Nov 21, 2025
    • Publications: details revised at 1 of 3 entries
    v18
  2. Minor Trial status: Recruiting to Active, Not Recruitingv17 Show 4 more changesShow less
    • Study sites: 12 to 11
    • Primary completion date: Sep 30, 2025 to Nov 2025
    • Study completion date: Oct 1, 2026 to Jul 2026
    • Publications: details revised at 1 of 3 entries
  3. Minor Primary completion date: Jul 31, 2025 to Sep 30, 2025
    • Study completion date: Mar 31, 2026 to Oct 1, 2026
    • Site details revised at 2 of 12 sites
    v16
  4. Minor Study sites: 10 to 12v15
  5. Minor Study sites: 11 to 10
    • Publications: details revised at 1 of 3 entries
    v14
Show 12 earlier versionsHide 12 earlier versions
  1. Minor Site contacts updated at 11 of 11 sites
    • Publications: details revised at 1 of 3 entries
    v13
  2. Minor Eligibility criteria expanded, about 7 wordsv12
  3. Minor Study sites: 10 to 11
    • Eligibility criteria expanded, about 19 words
    v11
  4. Minor Study sites: 7 to 10v10
  5. Minor Study sites: 5 to 7v9
  6. Minor Study sites: 2 to 5
    • Secondary endpoints: 13 to 5
    v8
  7. Minor Study sites: 1 to 2
    • Eligibility criteria expanded, about 28 words
    • Collaborators shortened, about 10 words
    • Study arms: 4 to 5
    v7
  8. Minor Start date changed from estimate of May 1, 2023 to May 8, 2023
    • Eligibility criteria shortened, about 8 words
    v6
  9. Notable Trial status: Not Yet Recruiting to Recruitingv5 Show 7 more changesShow less
    • Primary completion date: Nov 30, 2024 to Jul 31, 2025
    • Start date: Dec 1, 2022 to May 1, 2023
    • Study sites: 0 to 1
    • Study completion date: Jun 30, 2025 to Mar 31, 2026
    • Eligibility criteria expanded, about 242 words
    • Collaborators: 1 to 2
    • Publications: 2 to 3
  10. Notable Start date: Oct 1, 2022 to Dec 1, 2022v4 Show 6 more changesShow less
    • Primary completion date: Sep 30, 2024 to Nov 30, 2024
    • Eligibility criteria expanded, about 63 words
    • Secondary endpoints: details revised at 1 of 13 entries
    • Study arms: 5 to 4
    • Study description expanded, about 2 words
    • Study title expanded, about 5 words
  11. Minor Study title shortened, about 1 wordv3
  12. Notable Enrollment target: 45 to 70v2 Show 9 more changesShow less
    • Primary completion date: Dec 2020 to Sep 30, 2024
    • Start date: Sep 2019 to Oct 1, 2022
    • Primary endpoints: 1 to 2
    • Study completion date: Mar 2021 to Jun 30, 2025
    • Eligibility criteria expanded, about 292 words
    • Secondary endpoints revised (13)
    • Study description expanded, about 106 words
    • Study arms: 2 to 5
    • Collaborators expanded, about 5 words
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
2 trials monitored
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During the Efficacy Study (Part B), the investigators will study whether Pazopanib, taken daily for 24 weeks, will reduce the severity of nose bleeds in patients with hereditary hemorrhagic telangiectasia (HHT). Patients will either be provided active drug or a placebo \[sugar - inactive pill\], and be tested for nose bleed severity throughout the trial, including particularly nose bleed duration. Investigators will also test for blood loss, as well as for safety. This study is funded by the US Department of Defense USAMRAA and FDA/OOPD.
Trial Details
NCT Number NCT03850964
Lead Sponsor Cure HHT
Conditions
(from sponsor)
Hereditary Hemorrhagic Telangiectasia, Epistaxis, Anemia, Nosebleed, HHT
Related terms Anemia, Epistaxis, Telangiectasia, Hereditary Hemorrhagic
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov