Safety and Efficacy of ARA 290 in Sarcoidosis Patients with Symptoms of Small Fiber Neuropathy: A Randomized, Double-Blind Pilot Study

被引:83
作者
Heij, Lara [1 ]
Niesters, Marieke [1 ]
Swartjes, Maarten [1 ]
Hoitsma, Elske [2 ]
Drent, Marjolein [3 ,4 ]
Dunne, Ann [5 ]
Grutters, Jan C. [6 ,7 ]
Vogels, Oscar [8 ]
Brines, Michael [5 ]
Cerami, Anthony [1 ,5 ]
Dahan, Albert [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Anesthesiol, NL-2300 RC Leiden, Netherlands
[2] Diaconessenhuis, Dept Neurol, Leiden, Netherlands
[3] Univ Maastricht, Fac Hlth Med & Life Sci, Maastricht, Netherlands
[4] Hosp Gelderse Vallei, Dept Interstitial Lung, Ede, Netherlands
[5] Araim Pharmaceut, Ossining, NY USA
[6] St Antonius Hosp, Dept Pulmonol, Nieuwegein, Netherlands
[7] Univ Med Ctr Utrecht, Div Heart & Lungs, Utrecht, Netherlands
[8] St Antonius Hosp, Dept Neurol, Nieuwegein, Netherlands
关键词
TISSUE PROTECTION; ERYTHROPOIETIN; RECEPTOR;
D O I
10.2119/molmed.2012.00332
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ARA 290 (a peptide designed to activate the innate repair receptor that arrests injury and initiates cytoprotection, antiinflammation and healing) reduces allodynia in preclinical neuropathy models. We studied the safety and efficacy of ARA 290 to reduce symptoms of small fiber neuropathy (SFN) in patients with sarcoidosis. A total of 22 patients diagnosed with sarcoidosis and symptoms of SFN were enrolled in a double-blind, placebo-controlled exploratory trial consisting of three times weekly intravenous dosing of ARA 290 (2 mg; n = 12) or placebo (n = 10) for 4 wks. Inclusion criteria were a diagnosis of neuropathy and a spontaneous pain score of >= 5 (Brief Pain Inventory (BPI)). Endpoints assessed were changes in pain intensity and the small fiber neuropathy screening list (SFNSL) score, quality of life (SF-36), depressive symptoms (Inventory of Depressive Symptomatology (IDS)) and fatigue (Fatigue Assessment Scale (FAS)). No safety concerns were raised by clinical or laboratory assessments. The ARA 290 group showed significant (p < 0.05) improvement at wk 4 in SFNSL score compared with placebo (Delta -11.5 +/- 3.04 versus Delta -2.9 +/- 3.34 (standard error of the mean)). Additionally, the ARA 290 group showed a significant change from baseline in the pain and physical functioning dimensions of the SF-36 (Delta -23.4 +/- 5.5 and Delta -14.6 +/- 3.9, respectively). The mean BPI and FAS scores improved significantly but equivalently in both patient groups. No change was observed in the IDS. ARA 290 appears to be safe in patients with sarcoidosis and can reduce neuropathic symptoms. Online address: hffp://www.molmed.org doi: 10.2119/molmed.2012.00332
引用
收藏
页码:1430 / 1436
页数:7
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