Safety and Effectiveness of Sebetralstat for Short-Term Prevention Before Procedures in People With Hereditary Angioedema

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age12+
SponsorKalVista Pharmaceuticals, Ltd.

About this trial

This is a Phase 4, prospective, open-label trial to evaluate the safety and effectiveness of sebetralstat when used for STP for a qualifying procedures in patients 12 years of age or older with hereditary angioedema (HAE).

Eligibility criteria

Qualifiers

Male or female patients ≥12 years of age at time of Screening

Confirmed diagnosis of HAE Type I or II based on patient report

Patient has a qualifying procedure that is scheduled or planned to be scheduled to occur within 8 weeks of Screening

Patient has access to a commercial available on-demand treatment for HAE

Disqualifiers

A clinically significant history of poor response to bradykinin receptor 2 blocker, C1-INH therapy, or plasma kallikrein inhibitor therapy for the management of HAE, in the opinion of the Investigator

Use of angiotensin-converting enzyme (ACE) inhibitors within 7 days prior to the Screening Visit

Any estrogen-containing medications with systemic absorption (such as oral contraceptives including ethinylestradiol or hormonal replacement therapy) within 7 days prior to the Screening Visit

Patients who are taking strong cytochrome P450 (CYP)3A4 inhibitors or inducers or moderate CYP3A4 inducers within 2 weeks of the procedure

Trial design

Treatments tested in this trial

  • KVD900 600 mg

Treatment groups

100 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators