Related Experiment Video
Updated: Sep 5, 2025

Synthesis and Characterization of an Aspirin-fumarate Prodrug that Inhibits NFκB Activity and Breast Cancer Stem Cells
Published on: January 18, 2017
Dimethyl Fumarate as Therapeutic Alternative in Moderate-to-Severe Psoriasis: Our Experience
Pau Rosés Gibert1, Francisco Javier de la Torre Gomar1, Amaia Saenz Aguirre1
1Dermatology Department, Araba University Hospital, Vitoria-Gasteiz, Spain.
Purpose:
Dimethyl fumarate (DMF) is an oral formulation approved for the treatment of moderate-to-severe psoriasis in adult patients requiring systemic therapy. Here, we describe our clinical experience with DMF for moderate-to-severe psoriasis in Spain.
Patients And Methods:
This is a retrospective study including 30 adult patients with moderate-to-severe psoriasis under treatment with DMF between September 2018 and January 2020. Patients were treated with DMF as per its Summary of Product Characteristics and the median duration of treatment was 15 weeks (4-55 weeks). Psoriasis Area and Severity Index (PASI) and body surface area (BSA) severity scales were evaluated from baseline to week 36 and adverse events (AEs) developed during treatment were described.
Results:
The efficacy of DMF was assessed at week 8 and at week 36 (n = 5), both PASI and BSA were 0. At week 24, median PASI showed a decrease in both the last observation carried forward (LOCF; n = 23) and the observed cases (OC) (n = 10): from 10 to 6 and from 10 to 1.5, respectively. Median BSA also showed a decrease from 19 to 10 in LOCF and from 17 to 3 in OC. The most frequent AEs were diarrhoea (40.0%), flushing (13.3%) and lymphopenia (3.3%). In 47.1% patients, AEs have been solved by adjusting the DMF dose. Treatment discontinuation rate due to AEs was 43.3%.
Conclusion:
Our clinical experience indicates that DMF could be an effective and safe treatment for moderate-to-severe psoriasis in adult patients.
Insights
Dimethyl fumarate (DMF) effectively treats moderate-to-severe psoriasis in adults. This study shows significant PASI and BSA score reductions with manageable side effects, indicating DMF
Area of Science:
- Dermatology
- Pharmacology
Background:
- Dimethyl fumarate (DMF) is an approved oral therapy for moderate-to-severe psoriasis requiring systemic treatment.
- Psoriasis is a chronic autoimmune disease affecting skin, characterized by red, itchy, scaly patches.
Purpose of the Study:
- To evaluate the clinical experience and treatment outcomes of dimethyl fumarate (DMF) in adult patients with moderate-to-severe psoriasis in Spain.
- Assess the efficacy and safety profile of DMF for psoriasis management.
Main Methods:
- Retrospective study of 30 adult patients with moderate-to-severe psoriasis treated with DMF.
- Treatment duration ranged from 4 to 55 weeks, with a median of 15 weeks.
- Evaluated Psoriasis Area and Severity Index (PASI) and Body Surface Area (BSA) scores, and documented adverse events (AEs).
Main Results:
- Significant reductions in PASI and BSA scores observed by week 24.
- At week 36, 5 patients achieved PASI and BSA scores of 0.
- Most frequent adverse events included diarrhea (40.0%), flushing (13.3%), and lymphopenia (3.3%); 47.1% of AEs were managed by dose adjustment. Treatment discontinuation due to AEs occurred in 43.3% of patients.
Conclusions:
- Dimethyl fumarate (DMF) demonstrates efficacy in reducing psoriasis severity.
- DMF is a potentially safe and effective treatment option for adult patients with moderate-to-severe psoriasis.
- Adverse event management through dose adjustment is feasible, though discontinuation rates due to AEs should be considered.
Related Concept Videos
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents
Drugs for Treatment of Ulcerative Colitis in IBD
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids
Inflammatory Bowel Disease IV: Pharmacological Management
Pharmacologic...
Antiasthma Drugs: Leukotriene Modifiers
Leukotriene modifiers work through two distinct mechanisms:

