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Dose-ranging Study of Oral PHA-022121 for Prophylaxis Against Angioedema Attacks in Patients With Hereditary Angioedema Type I or Type II
Dose-ranging Study of Oral PHA-022121 for Prophylaxis Against Angioedema Attacks in Patients With Hereditary Angioedema Type I or Type II

NCT05047185

TerminatedPhase 2

Sponsor: Pharvaris Netherlands B.V.

Conditions: Hereditary Angioedema, Hereditary Angioedema Type I, Hereditary Angioedema Type II, Hereditary Angioedema Types I and II, Hereditary Angioedema Attack

Interventions: Deucrictibant low dose, Deucrictibant high dose, Placebo

Countries: United States, Austria, Bulgaria, Canada, Germany, Ireland, Italy, Poland

This study evaluates the safety and efficacy of PHA-022121 administered orally for prophylaxis against angioedema attacks in patients with hereditary angioedema (HAE). The study consists of 2 parts, with patients completing participation in Part 1 prior to initiation of treatment in Part 2. Part 1 of the study has 3 parallel arms and approximately 30 patients will be equally randomized to one of two dose regimens of PHA-022121 or matching placebo. Patients will continue to the single open-label arm in Part 2 of the study after completion of Part 1. The screening period is up to 8 weeks and the treatment periods are 12 weeks (Part 1) and 30 months (Part 2) in duration.

Eligibility overview

Sex: ALL

Age: 18 Years to 75 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Signed and dated informed consent form
* Diagnosis of HAE type I or II
* Documented history of at least 3 HAE attacks within the last 3 consecutive months prior to screening, or a minimum of 2 HAE attacks during the screening period
* Reliable access and experience to use standard of care acute attack medications

Exclusion Criteria:

* Pregnancy or breast-feeding
* Clinically significant abnormal electrocardiogram
* Any other systemic disease or significant disease or disorder that would interfere with the patient's safety or ability to participate in the study
* Use of C1-esterase inhibitor, oral kallikrein inhibitors, attenuated androgens, anti-fibrinolytics, or monoclonal HAE therapy within a defined period prior to enrolment
* Abnormal hepatic function
* Abnormal renal function
* History of alcohol or drug abuse within defined period, or current evidence of substance dependence or abuse
* Participation in any other investigational drug study within defined period
Locations (19)
  • Birmingham, Alabama, United States
  • Paradise Valley, Arizona, United States
  • St Louis, Missouri, United States
  • Vienna, Austria
  • Sofia, Bulgaria
  • Ottawa, Ontario, Canada
  • Montreal, Quebec, Canada
  • Berlin, Germany
  • Frankfurt, Germany
  • Dublin, Ireland
  • Padua, PD, Italy
  • Milan, Italy
  • Palermo, Italy
  • Krakow, Poland
  • Brighton, England, United Kingdom
  • Bristol, England, United Kingdom
  • Cambridge, England, United Kingdom
  • London, England, United Kingdom
  • Southampton, England, United Kingdom