» Articles » PMID: 32785877

Failed, Interrupted, or Inconclusive Trials on Immunomodulatory Treatment Strategies in Multiple Sclerosis: Update 2015-2020

Overview
Journal BioDrugs
Date 2020 Aug 14
PMID 32785877
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

In the past decades, multiple sclerosis (MS) treatment has experienced vast changes resulting from major advances in disease-modifying therapies (DMT). Looking at the overall number of studies, investigations with therapeutic advantages and encouraging results are exceeded by studies of promising compounds that failed due to either negative or inconclusive results or have been interrupted for other reasons. Importantly, these failed clinical trials are informative experiments that can help us to understand the pathophysiological mechanisms underlying MS. In several trials, concepts taken from experimental models were not translatable to humans, although they did not lack a well-considered pathophysiological rationale. The lessons learned from these discrepancies may benefit future studies and reduce the risks for patients. This review summarizes trials on MS since 2015 that have either failed or have been interrupted for various reasons. We identify potential causes of failure or inconclusiveness, looking at the path from basic animal experiments to clinical trials, and discuss the implications for our current view on MS pathogenesis, clinical practice, and future study designs. We focus on anti-inflammatory treatment strategies, without including studies on already approved and effective DMT. Clinical trials addressing neuroprotective and alternative treatment strategies are presented in a separate article.

Citing Articles

Alzheimer's disease and multiple sclerosis: a possible connection through the viral demyelinating neurodegenerative trigger (vDENT).

Boukhvalova M, Kastrukoff L, Blanco J Front Aging Neurosci. 2023; 15:1204852.

PMID: 37396655 PMC: 10310923. DOI: 10.3389/fnagi.2023.1204852.


Cladribine treatment improves cortical network functionality in a mouse model of autoimmune encephalomyelitis.

Schroeter C, Rolfes L, Gothan K, Gruchot J, Herrmann A, Bock S J Neuroinflammation. 2022; 19(1):270.

PMID: 36348455 PMC: 9641831. DOI: 10.1186/s12974-022-02588-7.


Impact of histone modifier-induced protection against autoimmune encephalomyelitis on multiple sclerosis treatment.

Jayaraman S, Jayaraman A Front Neurol. 2022; 13:980758.

PMID: 36313502 PMC: 9614082. DOI: 10.3389/fneur.2022.980758.


Autoreactive lymphocytes in multiple sclerosis: Pathogenesis and treatment target.

Liu R, Du S, Zhao L, Jain S, Sahay K, Rizvanov A Front Immunol. 2022; 13:996469.

PMID: 36211343 PMC: 9539795. DOI: 10.3389/fimmu.2022.996469.


Extracellular vesicles (exosomes and ectosomes) play key roles in the pathology of brain diseases.

Meldolesi J Mol Biomed. 2022; 2(1):18.

PMID: 35006460 PMC: 8607397. DOI: 10.1186/s43556-021-00040-5.


References
1.
Rojas O, Probstel A, Porfilio E, Wang A, Charabati M, Sun T . Recirculating Intestinal IgA-Producing Cells Regulate Neuroinflammation via IL-10. Cell. 2019; 176(3):610-624.e18. PMC: 6903689. DOI: 10.1016/j.cell.2018.11.035. View

2.
Ulzheimer J, Meuth S, Bittner S, Kleinschnitz C, Kieseier B, Wiendl H . Therapeutic approaches to multiple sclerosis: an update on failed, interrupted, or inconclusive trials of immunomodulatory treatment strategies. BioDrugs. 2010; 24(4):249-74. DOI: 10.2165/11537160-000000000-00000. View

3.
Koziol J, Lucero A, Sipe J, Romine J, Beutler E . Responsiveness of the Scripps neurologic rating scale during a multiple sclerosis clinical trial. Can J Neurol Sci. 1999; 26(4):283-9. DOI: 10.1017/s0317167100000391. View

4.
Darce J, Arendt B, Wu X, Jelinek D . Regulated expression of BAFF-binding receptors during human B cell differentiation. J Immunol. 2007; 179(11):7276-86. DOI: 10.4049/jimmunol.179.11.7276. View

5.
Agius M, Klodowska-Duda G, Maciejowski M, Potemkowski A, Li J, Patra K . Safety and tolerability of inebilizumab (MEDI-551), an anti-CD19 monoclonal antibody, in patients with relapsing forms of multiple sclerosis: Results from a phase 1 randomised, placebo-controlled, escalating intravenous and subcutaneous dose study. Mult Scler. 2017; 25(2):235-245. PMC: 6360486. DOI: 10.1177/1352458517740641. View