| NCT ID | Title | Phase | Status | Enrollment | Velocity | Design | Start | Completion | Last Updated | Sites | Countries |
|---|---|---|---|---|---|---|---|---|---|---|---|
| NCT00438815 | Open-Label C1 Esterase Inhibitor (C1INH-nf) for the Treatment of Acute Hereditary Angioedema (HAE) Attacks | PHASE3 | COMPLETED | 113 | — | — | Sep 21, 2006 | Mar 31, 2009 | Jun 8, 2021 | 30 | United States |
| NCT00462709 | Open-Label C1 Esterase Inhibitor (C1INH-nf) for the Prevention of Acute Hereditary Angioedema (HAE) Attacks | PHASE3 | COMPLETED | 146 | — | — | Jun 27, 2006 | Mar 31, 2009 | Jun 8, 2021 | 48 | United States |
| NCT00289211 | C1 Esterase Inhibitor (C1INH-nf) for the Treatment of Acute Hereditary Angioedema (HAE) Attacks | PHASE3 | COMPLETED | 83 | — | — | Mar 14, 2005 | Apr 13, 2007 | Jun 11, 2021 | 37 | United States |
| NCT01005888 | C1 Esterase Inhibitor (C1INH-nf) for the Prevention of Acute Hereditary Angioedema (HAE) Attacks | PHASE3 | COMPLETED | 26 | — | — | Mar 14, 2005 | Aug 22, 2007 | Jun 11, 2021 | 16 | United States |
| NCT00432510 | Pharmacokinetics of C1 Esterase Inhibitor in Hereditary Angioedema Subjects | PHASE1 | COMPLETED | 27 | — | — | Oct 9, 2006 | Feb 28, 2007 | Jun 3, 2021 | 6 | United States |
Subjects were to assess their symptoms every 15 minutes up to 4 hours after the initial dose or until substantial relief of the defining symptom was achieved. The conservative analysis defined substantial relief as 3 consecutive assessments of improvement of the defining symptom; any attack that did not have 3 consecutive documented reports of improvement was considered a treatment failure. In the less conservative analysis, attacks also were considered to have responded if clinical improvement of the defining symptom occurred but data were incomplete due to cessation of symptom assessments.
A hereditary angioedema (HAE) attack was defined as a discrete episode during which the subject progressed from no angioedema to symptoms of angioedema.
Randomized subjects assessed their symptoms every 15 minutes up to 4 hours after the initial dose of blinded study drug or until substantial relief of the defining symptom was achieved. Substantial relief was defined as 3 consecutive assessments of improvement of the defining symptom. Beginning of substantial relief was considered the first of the 3 consecutive assessments.
An HAE attack was defined as the subject-reported indication of swelling at any location following a report of no swelling on the previous day. Analyses include observed attack counts and normalized attack counts (i.e., the number of attacks observed during each therapy period, normalized for the number of days the subject participated in that period).
| Arm | Type | Description |
|---|---|---|
| Open-label C1INH-nf | EXPERIMENTAL | 1,000 Units (U) of C1INH-nf administered intravenously. If there was no response to treatment 60 minutes after the first dose, a second 1,000 U dose could be administered. |
| C1INH-nf | EXPERIMENTAL | 1,000 Units (U) of C1INH-nf administered intravenously (IV). If there was no response to treatment 60 minutes after the first dose, a second 1,000 U dose could be administered. |
| Placebo | PLACEBO_COMPARATOR | Matching placebo (saline) administered IV. If there was no response to treatment 60 minutes after the first dose, a second placebo (saline) dose could be administered. |
| C1INH-nf First, then Placebo | EXPERIMENTAL | 1,000 Units (U) of C1INH-nf administered intravenously (IV) every 3 to 4 days (approximately twice weekly) for 12 weeks, followed by matching placebo (saline) administered IV every 3 to 4 days for 12 weeks. |
| Placebo First, then C1INH-nf | EXPERIMENTAL | Matching placebo (saline) administered IV every 3 to 4 days (approximately twice weekly) for 12 weeks, followed by 1,000 U of C1INH-nf administered IV every 3 to 4 days for 12 weeks. |
| Single Dose | EXPERIMENTAL | 1,000 Units (U) of C1INH-nf administered intravenously (IV). |
| First Dose Followed by Second Dose | EXPERIMENTAL | 1,000 U of C1INH-nf administered IV, followed by a second 1,000 U dose 60 minutes later. |
| Name | Type | Description |
|---|---|---|
| C1 esterase inhibitor [human] (C1INH-nf) | BIOLOGICAL | - |
| Placebo (saline) | DRUG | - |
Inclusion Criteria: This study was open to all subjects who: * Completed participation in LEVP2005-1/A (NCT00289211) and were not participating in LEVP2005-1/B (NCT01005888), any time after the 3-day telephone follow-up * Completed participation in LEVP2005-1/B any time after the final prophylacti...
| Company | Ticker | Trials | Lead Phase | Drugs |
|---|---|---|---|---|
| Intellia Therapeutics, Inc. | NTLA | 3 | PHASE3 | NTLA-2002, Normal Saline Administration, Biological NTLA-2002 |
| BioCryst Pharmaceuticals, Inc. | BCRX | 2 | PHASE3 | Berotralstat, berotralstat |
| Ionis Pharmaceuticals, Inc. | IONS | 1 | PHASE3 | Donidalorsen |
| KalVista Pharmaceuticals, Inc. | KALV | 1 | PHASE3 | KVD900, Drug: KVD900 |
| Pharvaris N.V. | PHVS | 1 | PHASE2 | deucrictibant |
| BioMarin Pharmaceutical Inc. | BMRN | 1 | PHASE1 | Dose 1 of BMN 331 |
| Astria Therapeutics, Inc. | ATXS | 1 | PHASE2 | STAR-0215 |