Phase II study results of a replacement therapy for hereditary angioedema with subcutaneous C1‐inhibitor concentrate

Abstract

BackgroundHereditary angioedema (HAE) due to C1 inhibitor deficiency manifests as recurrent swelling attacks that can be disabling and sometimes fatal. Long‐term prophylaxis with twice‐weekly intravenous injections of plasma‐derived C1‐inhibitor (pdC1‐INH) has been established as an effective treatment. Subcutaneous (SC) administration of pdC1‐INH has not been studied in patients with HAE.MethodsThis open‐label, dose‐ranging, crossover study (COMPACT Phase II) was conducted in 18 patients with type I or II HAE who received two of twice‐weekly 1500, 3000, or 6000 IU SC doses of highly concentrated volume‐reduced CSL830 for 4 weeks each. The mean trough plasma levels of C1‐INH functional activity, C1‐INH and C4 antigen levels during Week 4, and overall safety and tolerability were evaluated. The primary outcome was model‐derived steady‐state trough C1‐INH functional activity.ResultsAfter SC CSL830 administration, a dose‐dependent increase in trough functional C1‐INH activity was observed. C1‐INH and C4 levels both increased. The two highest dose groups (3000 and 6000 IU) achieved constant C1‐INH activity levels above 40% values, a threshold that was assumed to provide clinical protection against angioedema attacks. Compared with intravenous injection, pdC1‐INH SC injection with CSL830 showed a lower peak‐to‐trough ratio and more consistent exposures. All doses were well tolerated. Mild‐to‐moderate local site reactions were noted with pain and swelling being the most common adverse event.ConclusionsSubcutaneous volume‐reduced CSL830 was well tolerated and led to a dose‐dependent increase in physiologically relevant functional C1‐INH plasma levels. A clinical outcome study of SC CSL830 in patients with HAE warrants further investigation.

Emerging Therapies in Hereditary Angioedema

“…7 Eighteen patients first received a single dose of Berinert 20U/kg IV within 2–7 days of receiving CSL830. The patients then received twice weekly subcutaneous injections of CSL830, a highly concentrated, volume-reduced C1-INH, for 4 weeks followed by a washout of 4 weeks and then received a different concentration of CSL830 for another 4 weeks.…”

The Role of Mast Cells Mediators in Angioedema Without Wheals

“…Recently, novel treatments have appeared for these types of angioedema, although we must keep in mind that much of the reported experience cited is from studies in HAE type I and II and further studies are needed to evaluate their efficacy in the others types of AE. [44]. Furthermore, the recent changes of product licences allowing self-administration provide additional options for the management of HAE and improve the quality of life of these patients [45].…”

Training patients for self‐administration of a new subcutaneous C1‐inhibitor concentrate for hereditary angioedema

“…A C1‐INH concentrate formulated for subcutaneous administration (C1‐INH[SC]; CSL830; HAEGARDA®; CSL Behring, Marburg, Germany) for the routine prevention of HAE attacks (Longhurst et al, ; Zuraw et al, ) was approved by the US FDA in 2017. Future approvals are anticipated in non‐US regions including Europe, Australia and Canada.…”