Stürner, K.H.K.H.StürnerStellmann, J.-P.J.-P.StellmannDörr, J.J.DörrPaul, F.F.PaulFriede, T.T.FriedeSchammler, S.S.SchammlerReinhardt, S.S.ReinhardtGellissen, S.S.GellissenWeissflog, G.G.WeissflogFaizy, T.D.T.D.FaizyWerz, O.O.WerzFleischer, S.S.FleischerVaas, L.A.I.L.A.I.VaasHerrmann, F.F.HerrmannPless, O.O.PlessMartin, R.R.MartinHeesen, C.C.Heesen2022-03-052022-03-052017https://publica.fraunhofer.de/handle/publica/25434710.1136/jnnp-2017-3171012-s2.0-85045073646Objective: To investigate whether oral administration of a standardised frankincense extract (SFE) is safe and reduces disease activity in patients with relapsing-remitting multiple sclerosis (RRMS). Methods: We performed an investigator-initiated, bicentric phase IIa, open-label, baseline-to-treatment pilot study with an oral SFE in patients with RRMS (NCT01450124). After a 4-month baseline observation phase, patients were treated for 8&#8201;months with an option to extend treatment for up to 36 months. The primary outcome measures were the number and volume of contrast-enhancing lesions (CEL) measured in MRI during the 4-month treatment period compared with the 4-month baseline period. Eighty patients were screened at two centres, 38 patients were included in the trial, 28 completed the 8-month treatment period and 18 of these participated in the extension period. Results: The SFE significantly reduced the median number of monthly CELs from 1.00 (IQR 0.75-3.38) to 0.50 (IQR 0.00-1.13; difference &#8722;0.625, 95%&#8201;CI &#8722;1.25 to &#8722;0.50; P<0.0001) at months 5-8. We observed significantly less brain atrophy as assessed by parenchymal brain volume change (P=0.0081). Adverse events were generally mild (57.7%) or moderate (38.6%) and comprised mainly gastrointestinal symptoms and minor infections. Mechanistic studies showed a significant increase in regulatory CD4+ T&#8201;cell markers and a significant decrease in interleukin-17A-producing CD8+ T cells indicating a distinct mechanism of action of the study drug. Interpretation: The oral SFE was safe, tolerated well and exhibited beneficial effects on RRMS disease activity warranting further investigation in a controlled phase IIb or III trial.en540571572A standardised frankincense extract reduces disease activity in relapsing-remitting multiple sclerosis (the SABA phase IIa trial)journal article