# A Study to Learn About the C1-Inhibitor Function as Diagnosis for Hereditary Angioedema

> **NCT07293364** · NA · NOT_YET_RECRUITING · sponsor: **Takeda** · enrollment: 514 (estimated)

## Conditions studied

- Hereditary Angioedema (HAE)

## Interventions

- **DIAGNOSTIC_TEST:** Technochrom C1-INH Kit

## Key facts

- **NCT ID:** NCT07293364
- **Lead sponsor:** Takeda
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-05-15
- **Primary completion:** 2027-01-07
- **Final completion:** 2027-01-07
- **Target enrollment:** 514 (ESTIMATED)
- **Last updated:** 2026-04-01

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07293364

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07293364, "A Study to Learn About the C1-Inhibitor Function as Diagnosis for Hereditary Angioedema". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT07293364. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*