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NCT03850730

Pazopanib for the Treatment of Epistaxis in Hereditary Hemorrhagic Telangiectasia

Status unknown Phase 1, PHASE2 Last updated 8 September 2022
What this trial tests

Phase 1, PHASE2 trial testing Pazopanib in Hereditary Hemorrhagic Telangiectasia in 30 participants. Status unknown.

Timeline
1 July 2023
Primary endpoint
30 June 2025
31 December 2025

Quick facts

Lead sponsorCure HHT
PhasePhase 1, PHASE2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date1 July 2023
Primary completion30 June 2025
Estimated completion31 December 2025

Drugs / interventions tested

Conditions studied

Sponsor

Cure HHT

Who can join

Adults 18 to 75, any sex, with Hereditary Hemorrhagic Telangiectasia or Epistaxis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Investigators will test the value of very low dose Pazopanib administered to patients with hereditary hemorrhagic telangiectasia for the reduction in the severity of nose bleeds in those with frequent and long duration bleeding episodes.

Publications & conference data

8 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Future treatments for hereditary hemorrhagic telangiectasia.
    Robert F, Desroches-Castan A, Bailly S, Dupuis-Girod S, et al · · 2020 · cited 76× · PMID 31910860 · DOI 10.1186/s13023-019-1281-4
  2. Review of Pharmacological Strategies with Repurposed Drugs for Hereditary Hemorrhagic Telangiectasia Related Bleeding.
    Albiñana V, Cuesta AM, Rojas-P I, Gallardo-Vara E, et al · · 2020 · cited 20× · PMID 32517280 · DOI 10.3390/jcm9061766
  3. Vascular malformations: An overview of their molecular pathways, detection of mutational profiles and subsequent targets for drug therapy.
    Mansur A, Radovanovic I. · · 2023 · cited 14× · PMID 36846125 · DOI 10.3389/fneur.2023.1099328
  4. Pathophysiology in Brain Arteriovenous Malformations: Focus on Endothelial Dysfunctions and Endothelial-to-Mesenchymal Transition.
    Jeong JY, Bafor AE, Freeman BH, Chen PR, et al · · 2024 · cited 6× · PMID 39200259 · DOI 10.3390/biomedicines12081795
  5. Targeted medical therapies for vascular anomalies.
    Borst A. · · 2024 · cited 1× · PMID 39644074 · DOI 10.1182/hematology.2024000599
  6. Vascular malformations: from genetics to therapeutics.
    Morin G, Galasso I, Canaud G. · · 2026 · PMID 41272322 · DOI 10.1038/s44321-025-00344-x
  7. Epistaxis Prevention, Treatment, and Future Perspectives for Hereditary Hemorrhagic Telangiectasia.
    Ficany A, Del Alamo M, Bernabeu C, Shovlin CL, et al · · 2025 · PMID 41227119 · DOI 10.3390/jcm14217724
  8. Pathogenesis and therapy of arteriovenous malformations: A case report and narrative review.
    Tessier S, Lipton BA, Ido F, Longo S, et al · · 2021 · PMID 34760664 · DOI 10.4103/ijciis.ijciis_127_20

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Other trials of Pazopanib

Trials testing the same drug.

Other recruiting trials for Hereditary Hemorrhagic Telangiectasia

Currently open trials in the same condition.

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Data sources for this page

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