Multiple Sklerose
Studienlage · Detail Klinische Studie · Multiple Sklerose · 2018

Tetrahydrocannabinol/Cannabidiol Oromucosal Spray in Patients With Multiple Sclerosis: A Pilot Study on the Plasma Concentration-Effect Relationship.

Klarer Nutzen GRADE Moderat 11 Zitate
Stichproben = 12 Pat.
Dauereinzelne Testdosis mit 240…
EndpunktNRS
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DesignKlinische Studie
Cannabinoidkombination
THC:CBD1:1
Applikationoromukosal
Kernaussage

Signifikante Reduktion der Spastizität (NRS-Scores von Median 6 auf 3.5, p<0.001) mit inverser Korrelation zu THC/CBD-Plasmakonzentrationen; keine signifikanten Effekte in motorischen Tests.

Zusammenfassung

Pilot-Studie n=12 MS-Patienten mit THC/CBD-Spray (2 Sprühstöße); Peak-Plasmakonzentrationen THC 0,60–13,29 ng/mL, CBD 0,55–11,93 ng/mL. NRS-Spastizitätsscore sank median von 6 auf 3,5 (p<0,001); signifikante inverse Korrelation zwischen NRS und THC-Plasmakonzentration (p<0,01) sowie CBD-Plasmakonzentration (p<0,002).

P
PopulationErwachsene mit Multipler Sklerose (chronisch behandelt), n=12
I
InterventionTHC/CBD-Oromukosalspray, 2 Sprühstöße im 15-Minuten-Abstand (Testdosis), subakute Einmalgabe
O
OutcomeNRS-Spastik-Score sank von Median 6 auf 3,5 (p<0,001); signifikante inverse Korrelation zwischen NRS und THC-Plasmakonzentration (p<0,01) sowie CBD-Plasmakonzentration (p<0,002); keine signifikanten Effekte in posturographischen und motorischen Tests
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Moderat

Dritte von vier GRADE-Stufen, die Effektschätzung ist wahrscheinlich verlässlich.

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Autoren
Contin M, Mancinelli L, Perrone A, Sabattini L, Mohamed S, Scandellari C, Foschi M, Vacchiano V, Lugaresi A, Riva R
DOI 10.1097/wnf.0000000000000294
Design: Klinische Studie
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Abstract
Objectives: We aimed to assess the potential relationship between intrasubject 9-tetrahydrocannabinol/cannabidiol (THC/CBD) oromucosal spray plasma profiles and clinical effects elicited by subacute dosing in chronically treated patients with multiple sclerosis (MS). Methods: The study design was pilot, single center, open, and prospective. The patients were challenged with a morning test dose of 2 THC/CBD sprays at a 15-minute interval. Venous blood samples were collected before the first spray administration and every 30 minutes after the second spray, until 240 minutes postdosing. Patients rated their spasticity by the Numerical Rating Scale (NRS) simultaneously with blood drawings. Postural and motor tests were performed before the first spray and 90 and 180 minutes thereafter. Results: Twelve patients were recruited. Peak plasma concentrations of THC/CBD largely varied among patients, from 0.60 to 13.29 ng/mL for THC and 0.55 to 11.93 ng/mL for CBD. Time to peak plasma concentrations ranged from 150 to 240 minutes for THC and 90 to 240 minutes for CBD. Patients' NRS serial scores decreased after dosing, from a median value of 6 to 3.5 (P < 0.001). A significant inverse correlation was observed between median intrasubject repeated NRS scores and corresponding median values of both THC (P < 0.01) and CBD (P < 0.002) plasma concentrations. No significant effect of cannabinoids dosing could be appreciated according to posturographic and motor tests. Conclusions: Our kinetic dynamic findings from THC/CBD oromucosal spray are the first obtained in real MS patients. Although preliminary, they suggest that subacute dosing might elicit a subjective clinically significant effect on MS-related spasticity, paralleling cannabinoids measurable plasma concentrations.

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