Universität zu Köln

Huntgeburth, Michael, Kiessling, Johannes, Weimann, Gerrit, Wilberg, Verena, Saleh, Soundos, Hunzelmann, Nicolas and Rosenkranz, Stephan (2018). Riociguat for the Treatment of Raynaud's Phenomenon: A Single-Dose, Double-Blind, Randomized, Placebo-Controlled Cross-Over Pilot Study (DIGIT). Clin. Drug Invest., 38 (11). S. 1061 - 1070. NORTHCOTE: ADIS INT LTD. ISSN 1179-1918

Full text not available from this repository.

Abstract

Background and Objective Raynaud's phenomenon (RP) is characterized by transient digital ischemia and is commonly associated with connective tissue disease. Treatment remains unsatisfactory. Here we evaluate the efficacy, safety, and pharmacokinetics of a single dose of the soluble guanylate cyclase stimulator riociguat in RP. Methods DIGIT was a double-blind, randomized, placebo-controlled pilot study. Patients with primary or secondary RP were randomized to a single oral dose of riociguat 2mg or placebo in a cross-over design (73days). Efficacy was assessed as placebo-corrected change in digital blood flow 2h post-dose at room temperature (RT) or following cold exposure (CE), measured by laser-speckle contrast analysis. Patients were regarded as responders if placebo-corrected digital blood flow increased by10% from baseline at RT or after CE. Results Of 20 eligible patients, 17 (85%) were female and mean [standard deviation (SD)] age was 52 (13.8) years. Placebo-corrected changes in digital blood flow were + 46% [90% confidence interval (CI) -6 to + 98] at RT and -9% (90% CI -63 to + 44) after CE, with high inter-individual variability. Eight patients (40%) were responders at RT, and 12 (60%) after CE. Riociguat increased mean (SD) digital blood flow in responders at RT by + 136% (114) and in responders following CE by + 39% (53). Riociguat was well tolerated, with few adverse events. Conclusion In this pilot study, single-dose riociguat was well tolerated in patients with RP and resulted in improved digital blood flow in some patient subsets, with high inter-individual variability. Long-term evaluation is warranted.

Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Huntgeburth, Michael UNSPECIFIED UNSPECIFIED UNSPECIFIED Kiessling, Johannes UNSPECIFIED UNSPECIFIED UNSPECIFIED Weimann, Gerrit UNSPECIFIED UNSPECIFIED UNSPECIFIED Wilberg, Verena UNSPECIFIED UNSPECIFIED UNSPECIFIED Saleh, Soundos UNSPECIFIED UNSPECIFIED UNSPECIFIED Hunzelmann, Nicolas UNSPECIFIED UNSPECIFIED UNSPECIFIED Rosenkranz, Stephan UNSPECIFIED UNSPECIFIED UNSPECIFIED
URN:	urn:nbn:de:hbz:38-168342
DOI:	10.1007/s40261-018-0698-1
Journal or Publication Title:	Clin. Drug Invest.
Volume:	38
Number:	11
Page Range:	S. 1061 - 1070
Date:	2018
Publisher:	ADIS INT LTD
Place of Publication:	NORTHCOTE
ISSN:	1179-1918
Language:	English
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language SOLUBLE GUANYLATE-CYCLASE; PATHOGENESIS; SCLERODERMA; MANAGEMENT; SILDENAFIL; DIAGNOSIS; CONSENSUS Multiple languages Pharmacology & Pharmacy Multiple languages
Refereed:	Yes
URI:	http://kups.ub.uni-koeln.de/id/eprint/16834