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NCT03850730
Pazopanib for the Treatment of Epistaxis in Hereditary Hemorrhagic Telangiectasia
Phase 1, PHASE2 trial testing Pazopanib in Hereditary Hemorrhagic Telangiectasia in 30 participants. Status unknown.
30 June 2025
Quick facts
| Lead sponsor | Cure HHT |
|---|---|
| Phase | Phase 1, PHASE2 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 1 July 2023 |
| Primary completion | 30 June 2025 |
| Estimated completion | 31 December 2025 |
Drugs / interventions tested
- Pazopanib — full drug profile →
Conditions studied
- Hereditary Hemorrhagic Telangiectasia — all drugs for Hereditary Hemorrhagic Telangiectasia →
- Epistaxis — all drugs for Epistaxis →
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):
-
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 -
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 -
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 -
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 -
Targeted medical therapies for vascular anomalies.
Borst A. · · 2024 · cited 1× · PMID 39644074 · DOI 10.1182/hematology.2024000599 -
Vascular malformations: from genetics to therapeutics.
Morin G, Galasso I, Canaud G. · · 2026 · PMID 41272322 · DOI 10.1038/s44321-025-00344-x -
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 -
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
Verify or expand the search:
- PubMed search for NCT03850730
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Related trials
Other trials of Pazopanib
Trials testing the same drug.
- NCT07444619 — A Phase I Study of Pazopanib in Combination With Trabectedin, Ipilimumab and Nivolumab (TraPIN) in Pediatric and Young A · Phase 1 · not yet recruiting
- NCT07087158 — A Study of IBR854 Combined With Pazopanib Versus Pazopanib in Advanced Renal Cell Carcinoma · Phase 2 · not yet recruiting
- NCT04199026 — Implantable Microdevice for the Delivery of Drugs and Their Effect on Tumors in Patients With Metastatic or Recurrent Sa · NA · recruiting
- NCT05432791 — Testing Olaparib and Temozolomide Versus the Usual Treatment for Uterine Leiomyosarcoma After Chemotherapy Has Stopped W · Phase 2, PHASE3 · active not recruiting
- NCT02203760 — Pazopanib Vs. Pazopanib Plus Gemcitabine · Phase 2 · active not recruiting
Other recruiting trials for Hereditary Hemorrhagic Telangiectasia
Currently open trials in the same condition.
- NCT06659640 — A Study to Evaluate ALN-6400 in Healthy Volunteers and Patients With Hereditary Hemorrhagic Telangiectasia (HHT) · Phase 1, PHASE2 · recruiting
- NCT04874558 — Ultra-low-dose Chest CT for HHT · active not recruiting
- NCT04404881 — Bevacizumab In Hereditary Hemorrhagic Telangiectasia · Phase 2 · active not recruiting
- NCT04469517 — Influence of Hypoxic Induced Factors in Patients With Hereditary Hemorrhagic Telangiectasia · recruiting
- NCT04150822 — CHORUS - Comprehensive HHT Outcomes Registry of the United States (Formerly OUR HHT Registry) · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03850730 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Cure HHT
- Last refreshed: 8 September 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03850730.
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