Diroximel fumarate (DRF) is a novel oral fumarate approved in the USA for relapsing forms of multiple sclerosis. DRF is converted to monomethyl fumarate, the pharmacologically active metabolite of dimethyl fumarate (DMF). DRF 462 mg and DMF 240 mg produce bioequivalent exposure of monomethyl fumarate and are therefore expected to have similar efficacy/safety profiles; the distinct chemical structure of DRF may contribute to its tolerability profile.
The objective of this study was to compare the gastrointestinal tolerability of DRF and DMF over 5 weeks in patients with relapsing–remitting multiple sclerosis.
EVOLVE-MS-2 was a phase III, randomized, double-blind, head-to-head, 5-week study evaluating the gastrointestinal tolerability of DRF 462 mg vs DMF 240 mg, administered twice daily in patients with relapsing–remitting multiple sclerosis, using two self-administered gastrointestinal symptom scales: Individual Gastrointestinal Symptom and Impact Scale (IGISIS) and Global Gastrointestinal Symptom and Impact Scale (GGISIS). The primary endpoint was the number of days with an IGISIS intensity score ≥ 2 relative to exposure. Other endpoints included the degree of gastrointestinal symptom severity measured by IGISIS/GGISIS and assessment of safety/tolerability.
DRF-treated patients experienced a statistically significant reduction (46%) in the number of days with an IGISIS symptom intensity score ≥ 2 compared with DMF-treated patients (rate ratio [95% confidence interval]: 0.54 [0.39–0.75]; p = 0.0003). Lower rates of gastrointestinal adverse events (including diarrhea, nausea, vomiting, and abdominal pain) were observed with DRF than DMF (34.8% vs 49.0%). Fewer patients discontinued DRF than DMF because of adverse events (1.6% vs 5.6%) and gastrointestinal adverse events (0.8% vs 4.8%).
DRF demonstrated an improved gastrointestinal tolerability profile compared with DMF, with less severe gastrointestinal events and fewer days of self-assessed gastrointestinal symptoms, fewer gastrointestinal adverse events, and lower discontinuation rates because of gastrointestinal adverse events.
Clinical Trials Registration
|EVOLVE-MS-2 was a 5-week head-to-head study evaluating the gastrointestinal tolerability of diroximel fumarate (DRF) vs dimethyl fumarate (DMF) in patients with relapsing–remitting multiple sclerosis.|
|DRF-treated patients reported less severe gastrointestinal events lasting fewer days compared with patients treated with DMF.|
|Patients treated with DRF had lower rates of treatment discontinuation due to gastrointestinal adverse events than patients treated with DMF.|
Diroximel fumarate (DRF) is a novel oral fumarate approved in the USA for the treatment of patients with relapsing forms of multiple sclerosis (MS) . DRF undergoes esterase cleavage to monomethyl fumarate, the same pharmacologically active metabolite as the approved drug Tecfidera® (delayed-release dimethyl fumarate [DMF]) . When administered orally at doses of 462 mg and 240 mg, respectively, DRF and DMF yield bioequivalent exposure of monomethyl fumarate and therefore are expected to have similar efficacy and safety profiles . DMF has demonstrated significant and clinically meaningful efficacy, and a well-tolerated safety profile in clinical trials and real-world studies, totaling > 810,000 patient-years of exposure [4,5,6,7,8].
Gastrointestinal (GI) adverse events (AEs) such as nausea, vomiting, abdominal pain, and diarrhea are not uncommon with DMF, particularly in the first month of treatment [4, 5, 9]. In the pivotal DEFINE/CONFIRM trials (n = 1540), the incidence of GI AEs was 40% and led to treatment discontinuation in 4% of patients [2, 10]. In a real-world study, up to 88% of patients treated with DMF reported GI events when self-assessing GI symptoms using eDiaries . Although GI symptom management and mitigation approaches have been developed, DMF treatment discontinuation because of GI AEs still occurs and varies between 5 and 19% in real-world studies [11, 12].
The distinct chemical structure of DRF is hypothesized to elicit less irritation in the GI tract than DMF through lower production of methanol (a GI-irritating promoiety), and less reactivity with pre-systemic off-target proteins or receptors . Interim findings from the ongoing, multicenter, 2-year, prospective, single-arm, open-label DRF phase III EVOLVE-MS-1 study have demonstrated a low rate (~ 31%) of GI AEs when considered within the context of those reported in separate clinical trials and real-world effectiveness studies of DMF [9, 10, 14]. Notably, < 1% of patients in the EVOLVE-MS-1 study discontinued DRF treatment because of GI AEs . However, it is challenging to make any conclusions about differences in the GI tolerability profile between DRF and DMF in the absence of head-to-head data.
Herein, we present final study results from the EVOLVE-MS-2 study, which was designed to compare GI tolerability of DRF with DMF over 5 weeks in adults with relapsing–remitting MS (RRMS). The EVOLVE-MS-2 study objectives were to (1) evaluate the utility of two GI symptom scales (Individual Gastrointestinal Symptom and Impact Scale [IGISIS] and Global Gastrointestinal Symptom and Impact Scale [GGISIS]); (2) compare GI tolerability of DRF with DMF using these two GI symptom scales; and (3) evaluate the overall safety and tolerability of DRF, including the incidence of GI AEs and number of study withdrawals because of GI AEs in adults with RRMS.
EVOLVE-MS-2 (NCT03093324) was a 5-week, randomized, double-blind, head-to-head, phase III study designed to evaluate GI tolerability of DRF 462 mg vs DMF 240 mg administered twice daily in patients with RRMS. Patients utilized two eDiary symptom scales to evaluate the duration and severity of GI symptoms on a daily basis: IGISIS and GGISIS. In addition, AEs were collected by investigators at weekly study visits. The study included a ≤ 4-week screening period, a 5-week double-blind treatment period with two blinded treatment groups, and a 2-week follow-up period (Fig. 1). The screening period included a 1-week lead-in period, prior to randomization, during which patients completed the two self-administered GI symptom scales daily to test for eDiary compliance and/or underlying baseline GI symptoms.
Block randomization was performed using a block size of 4. Patients were randomized 1:1 into one of the two treatment groups, and all patients received two capsules twice daily for all doses to maintain blinding. Patients received either DRF at the approved dose of 231 mg twice daily (administered as one 231-mg capsule and one placebo capsule twice daily) for week 1 followed by DRF 462 mg twice daily (administered as two 231-mg capsules twice daily) for weeks 2–5 (group 1), or DMF at the approved dose of 120 mg twice daily (administered as one 120-mg capsule and one placebo capsule twice daily) for week 1 followed by DMF 240 mg twice daily (administered as one 240-mg capsule and one placebo capsule twice daily) for weeks 2–5 (group 2). The treatment period was double-blind; DMF capsules were over-encapsulated to create the blinded study drug. Patients were instructed to take the study drug with or without food, but to avoid a high-fat and high-calorie meal (defined as > 1000 calories and containing 50 g of fat) to ensure adequate levels of monomethyl fumarate [2, 3]. No dose reductions were permitted during the study. Symptomatic therapies for tolerability events were permitted and recorded as concomitant medications.
The study utilized an adaptive study design, an approach that allows for planned modifications to ongoing trials (such as changes to trial parameters or statistical procedures) using pre-specified interim data analyses, without compromising trial integrity or validity [15, 16]. Adaptive trial design has been used to re-estimate sample size in instances in which variances of the response variables are unknown, as was the case with the novel endpoints used in the EVOLVE-MS-2 study . In this study, it was initially hypothesized that comparing DRF and DMF using the IGISIS intensity scale would detect a difference between the two groups. As there was no previous experience with the IGISIS and GGISIS scales to inform statistical assumptions, a pre-planned unblinded analysis of data was conducted after the first 120 patients were randomized (i.e., part A), in which the objectives were to assess the utility of the GI symptom scales; refine the primary endpoint to select the most sensitive measure for detecting a difference between DRF and DMF; and inform the sample size. From this analysis, the IGISIS endpoint was modified from ≥ 3 to ≥ 2 as the latter was deemed to be the more sensitive indicator. All patients, investigators, and sites remained blinded to the part A data to preserve the integrity of the trial. After the initial 120 patients, the subsequently randomized patients (i.e., part B) were enrolled, bringing the overall planned population to 500 patients. Patients who completed the 5-week treatment period were eligible to enroll in the EVOLVE-MS-1 (ClinicalTrials.gov [NCT02634307]) long-term, open-label, DRF safety study .
Eligible patients were aged 18–65 years, had a confirmed diagnosis of RRMS , and were neurologically stable with no evidence of relapse in the 30 days prior to screening. Patients were not eligible to participate if they had a history of GI surgery (except appendectomy that occurred > 6 months prior to screening); clinically significant recurring or active GI symptoms within 3 months of screening or long-term use of medical therapy to treat GI symptoms within 1 month of screening; or two or more IGISIS intensity scores of ≥ 3 during the 1-week lead-in period prior to randomization. Patients who had previously received fumarate treatment were also prohibited from study enrollment. The study was approved by central and local ethics committees and was conducted in accordance with the International Council on Harmonisation Guidelines for Good Clinical Practice and the Declaration of Helsinki. All patients provided written informed consent.
The primary endpoint was the number of days, relative to exposure, with any IGISIS intensity score ≥ 2 in the overall study population. Secondary endpoints included the number of days, relative to exposure, with: (1) an IGISIS intensity score ≥ 2 in part B only; (2) an IGISIS intensity score ≥ 1 in the overall population; (3) an IGISIS intensity score ≥ 3 in the overall population; (4) a GGISIS symptom intensity score ≥ 1 in the overall population; (5) a GGISIS symptom intensity score ≥ 2 in the overall population; (6) a GGISIS symptom intensity score ≥ 3 in the overall population; and (7) worst (i.e., highest) IGISIS individual symptom intensity score by week during the 5-week treatment period in the overall population.
Pre-specified exploratory endpoints included the number of days relative to exposure with an IGISIS intensity score of ≥ 1 and ≥ 3, or a GGISIS intensity score of ≥ 1, ≥ 2, or ≥ 3, in part B only. Investigator-assessed AEs were summarized.
Gastrointestinal tolerability was assessed using two novel GI symptom scales, IGISIS and GGISIS. The scales were adapted from the Modified Acute Gastrointestinal Symptom Scale (MAGISS) and the Modified Overall Gastrointestinal Symptom Scale (MOGISS) used in trials with DMF, which have been previously described [9, 19]. The IGISIS is a questionnaire designed to capture the incidence, intensity, onset, duration, and functional impact of five key individual GI symptoms: nausea, vomiting, upper abdominal pain, lower abdominal pain, and diarrhea (Fig. S1a in the Electronic Supplementary Material [ESM]). In the DMF pivotal DEFINE/CONFIRM trials, these specific GI symptoms were among the most commonly reported AEs and were the most common GI AEs leading to treatment discontinuation [4, 5, 20]. Patients were instructed to self-administer the IGISIS questionnaire twice per day within 9 h of taking the study drug, using an eDiary. The patient rated the severity of each symptom on a scale of 0 (did not have) to 10 (extreme); for each symptom, patients also recorded duration and rated interference on daily activities using a 5-point Likert scale (Fig. S1a in the ESM).
The GGISIS is designed to assess the overall intensity of five GI symptoms (nausea, vomiting, upper abdominal pain, lower abdominal pain, and diarrhea) experienced during the previous 24 h, the level of interference and functional impact on work and daily activities, and how bothersome GI symptoms were for patients. To rate the intensity of GI symptoms and assess how bothersome GI symptoms were, patients completed the questionnaire once per day using a scale of 0 (did not have) to 10 (extreme). Patients also recorded the level of interference and impact of GI symptoms on daily activities and work (Fig. S1b in the ESM).
Safety assessments included AEs (including GI AEs), vital signs, clinical laboratory tests (chemistry, hematology, and urinalysis), and electrocardiogram findings. Adverse events were assessed by the investigator at weekly visits and recorded by severity and relatedness.
Analysis Populations and Statistics
Gastrointestinal tolerability was assessed in all patients who received at least one dose of the study drug and completed at least one post-baseline GI tolerability assessment. Data collected from patients in the overall population were analyzed for the primary endpoint; secondary endpoints assessed data from the overall population, as well as for part B separately.
Based on the pre-planned unblinded analysis of the first 120 patients (part A data), it was assumed that the number of days with an IGISIS intensity score of ≥ 2 relative to exposure in the treatment period would be 2.0 days for DRF and 3.5 days for DMF. Using a negative binomial regression approach with a two-sided α-level of 0.05, it was estimated that an enrollment size of 500 total patients would provide ~ 80% power to detect a ≥ 42% reduction in the relative rate for DRF vs DMF. The number of days with any IGISIS individual symptom intensity score relative to exposure days was analyzed using a negative binomial regression model with treatment as a factor and adjusted for study parts, region, age, and body mass index. The worst IGISIS individual symptom intensity score during the treatment period was summarized by treatment group and analyzed using an analysis of covariance model with treatment as a factor and adjusted for study parts, region, age, and body mass index. Safety analyses were summarized for all patients who received at least one dose of the study drug.
A total of 854 patients underwent screening; 506 patients were randomized and 504 patients received at least one dose of the study drug (Fig. S2 in the ESM). Baseline demographics and disease characteristics were generally well balanced. Approximately 50% of patients were enrolled from the USA (Table 1). Most patients completed the study (94.8%, 478/504), 97.1% (464/478) of whom rolled over into the EVOLVE-MS-1 study. The rate of discontinuation was lower for patients treated with DRF compared with DMF (3.2% vs 7.2%, respectively). This difference in rate of discontinuation was predominantly attributable to the difference in the rate of AEs leading to discontinuation (1.6% for DRF-treated patients compared with 5.6% for DMF-treated patients). Other reasons for discontinuation were similar between the two groups (Table 2).
For the analysis of self-assessed GI events, 502 patients were eligible for inclusion in the analysis; 253 were assigned to DRF and 249 were assigned to DMF. For the IGISIS analyses, mean (standard deviation [SD]) exposure days were comparable for the two groups: 35.2 (4.2) days for DRF-treated patients and 34.2 (5.9) days for DMF-treated patients. When analyzing the part B population separately, 194 DRF-treated and 191 DMF-treated patients were included. Mean (SD) exposure in the part B population was similar to that of the overall population: 35.2 (3.8) days for DRF and 33.7 (6.3) days for DMF. For the GGISIS analyses, mean (SD) exposure days with at least one diary available for analysis were lower than that observed with IGISIS, yet comparable between the two groups: 33.3 (4.8) days for DRF and 32.6 (5.6) days for DMF.
Patient Self-Assessed Gastrointestinal Tolerability
The number of days with an IGISIS intensity score of ≥ 2 relative to exposure was statistically significantly lower with DRF compared with DMF. The adjusted mean (95% confidence interval [CI]) number of days with a patient-assessed event was 1.4 (1.1‒1.9) days with DRF and 2.6 (2.0‒3.3) days with DMF. The adjusted rate ratio (95% CI) was 0.54 (0.39–0.75), representing a 46% reduction (p = 0.0003; Fig. 2). A sensitivity analysis was performed to include only diaries completed as instructed (within 2–9 h of dosing). The mean (SD) number of evaluable days with diaries completed as instructed were similar for the two groups: 25.8 (11.8) for DRF and 26.1 (11.0) for DMF. Among diaries completed as instructed, the adjusted mean (95% CI) number of days with an IGISIS score of ≥ 2 relative to exposure was 1.0 (0.8‒1.3) for DRF and 2.1 (1.6‒2.9) for DMF, resulting in an adjusted rate ratio (95% CI) of 0.49 (0.34–0.70); this represented a 51% reduction (p < 0.0001).
When symptom intensity and frequency was assessed using a GGISIS intensity score of ≥ 2, there were fewer days of events with DRF compared with DMF, although the difference was not statistically significant. Patients treated with DRF reported 1.1 (0.8‒1.5) adjusted mean (95% CI) days with a GGISIS score of ≥ 2 compared with 1.6 (1.1‒2.2) days for DMF-treated patients in the overall population. The adjusted rate ratio (95% CI) was 0.67 (0.43–1.05; p = 0.082; Fig. 2).
In a comparison using an IGISIS intensity score of ≥ 1, the adjusted mean (95% CI) number of days relative to exposure was significantly lower with DRF (3.0 [2.5‒3.7]) compared with DMF (4.1 [3.4‒5.0]). The rate ratio (95% CI) was 0.71 (0.55–0.92), representing a 29% reduction (p = 0.009; Fig. 2). The number of days relative to exposure with an IGISIS intensity score of ≥ 3 was 44% lower with DRF than DMF (rate ratio [95% CI]: 0.56 [0.36‒0.86]; p = 0.009). Similarly, there were fewer days with a GGISIS intensity score of ≥ 1 (rate ratio [95% CI]: 0.70 [0.50–0.98]) and ≥ 3 (0.74 [0.43–1.28]) with DRF than DMF over the study period (Fig. 2).
In an analysis of data collected from part B only, the number of days with an IGISIS intensity score of ≥ 2 relative to exposure was statistically significantly lower with DRF compared with DMF. The adjusted mean (95% CI) number of days with a patient-assessed event for DRF-treated patients was 1.2 (0.9‒1.5) days compared with 2.1 (1.7‒2.8) days for DMF-treated patients. The adjusted rate ratio (95% CI) was 0.52 (0.36–0.76), representing a 48% reduction (p = 0.0007; Fig. 3). Reductions consistent with those observed in the overall population were also noted when comparing DRF and DMF using IGISIS intensity scores of ≥ 1 (p = 0.01) and ≥ 3 (p = 0.012) and GGISIS intensity scores of ≥ 1 (p = 0.028), ≥ 2, and ≥ 3 in the part B-only population (Fig. S3 in the ESM).
Symptom severity was assessed using data collected from the IGISIS eDiary. Over the course of the 5-week treatment period, patients recorded an overall least squares (LS) mean (standard error [SE]) worst IGISIS symptom intensity score of 2.0 (0.2) if treated with DRF and 2.4 (0.2) if treated with DMF (p = 0.069; Fig. 4). During the 1-week titration period, LS mean (SE) worst symptom score was 1.0 (0.1) for DRF vs 0.8 (0.1) for DMF. However, following the titration period, LS mean (SE) worst symptom intensity score peaked after the first week of the full-dose study drug for DMF-treated patients (DMF week 3, 1.4 [0.1]), before declining by the end of treatment (DMF week 5, 0.6 [0.1]). In contrast, DRF-treated patients experienced a gradual decline in LS mean (SE) worst symptom score over the course of treatment (DRF week 3, 0.9 [0.1]; week 5, 0.5 [0.1]). Statistically significant differences with DRF vs DMF were observed in week 3 (DRF: 0.9 [0.1] vs DMF: 1.4 [0.1], p = 0.002) and week 4 (DRF: 0.6 [0.1] vs DMF: 1.0 [0.1], p = 0.004). The IGISIS worst symptom intensity scores were lower with DRF than DMF for events associated with the upper GI tract (with statistically significant reductions observed for nausea, vomiting, upper abdominal pain) but similar for events associated with the lower GI tract (diarrhea, lower abdominal pain; Table 3).
Fewer patients treated with DRF categorized their GI events as interfering “quite a bit” or “extremely” with the ability to accomplish daily activities when assessed using both IGISIS and GGISIS scales, compared with patients treated with DMF: nausea (2.4% vs 6.8%), vomiting (1.2% vs 5.6%), upper abdominal pain (1.2% vs 6.8%), lower abdominal pain (1.2% vs 3.2%), diarrhea (3.6% vs 6.4%), and all GI events (GGISIS, 7.9% vs 10.8%; Table S1 in the ESM). In addition, a higher percentage of patients treated with DRF assessed the impact of their GI events as “not at all” affecting work productivity (47.8%, 121/253) compared with DMF (40.6%, 101/249), and for those reporting employment and missed hours at work because of GI events (DRF, 20/133; DMF, 26/133) the mean (SD) greatest number of hours missed was lower for patients treated with DRF than DMF: 4.3 (3.7) and 5.5 (4.8), respectively.
Overall, AEs were reported in 81% (408/504) of patients (DRF, 78.3%; DMF, 83.7%; Table 4). Most AEs were mild to moderate in severity (DRF, 97.5% [193/198]; DMF, 93.3% [196/210]; Table 4). The overall rate of serious AEs was low (1.4%; four patients with DRF and three patients with DMF); none were related to the study drug. No deaths were reported. Gastrointestinal AEs were among the most frequently reported; 34.8% in the DRF treatment group and 49.0% in the DMF treatment group. In particular, GI AEs associated with an upper GI location (upper abdominal pain, nausea, vomiting) appeared to be reported with less frequency in patients treated with DRF compared with DMF (Table 5). Overall, 19.3% (17/88) of patients in the DRF group and 30.6% (37/121) of patients in the DMF group used concomitant medications to treat GI-related AEs during the treatment period. Two patients in the DMF group experienced a GI AE that was not considered tolerability related (toothache, n = 1; dry mouth, n = 1) and were excluded from the analysis. Flushing was reported in 36.7% of patients overall (DRF, 32.8%; DMF, 40.6%).
The incidence of AEs leading to treatment discontinuation was lower for patients treated with DRF (1.6%) compared with DMF (5.6%). Gastrointestinal AEs led to discontinuation in 0.8% of patients treated with DRF and 4.8% of patients treated with DMF. No patients in either treatment group discontinued because of lack of efficacy.
Results from the EVOLVE-MS-2 study demonstrate that DRF has an improved GI tolerability profile compared with DMF. Tolerability is an important factor for drug adherence and achievement of maximal efficacy, particularly for medications used for long-term management of chronic diseases such as MS . This randomized double-blind study was specifically designed to assess the duration and severity of key GI events: nausea, vomiting, diarrhea, and upper and lower abdominal pain.
EVOLVE-MS-2 is the first study to directly compare the GI tolerability profiles of two MS treatments. Patients treated with DRF reported significantly fewer days with GI events, with an IGISIS severity score of ≥ 2 over a 5-week period, than patients treated with DMF. This finding, which favored DRF, was consistently observed across comparisons using different severity score thresholds on both IGISIS and GGISIS. The observed differences in days with GI events and severity of GI events as assessed by the patient were supported by lower rates of investigator-assessed GI AEs and GI AEs leading to treatment discontinuation in DRF-treated patients. In addition, patients treated with DRF tended to report that GI events were less likely to interfere with their daily activities, less bothersome, and less likely to impact work productivity and absenteeism. Although the absolute difference in number of days with GI events with DRF and DMF as measured by IGISIS was small, the improvements observed with DRF support clinically meaningful and relevant outcomes such as fewer treatment discontinuations, less patient-reported interference of GI symptoms, and fewer effects on work productivity. The timing of treatment benefit is also important. Most (91.7%; 11/12) DMF treatment discontinuations in EVOLVE-MS-2 occurred by week 3. Therefore, although worst GI symptom severity scores with DRF and DMF tend to be similar by week 5 (Fig. 4), the early differences observed by week 3 appear to provide meaningful patient benefit.
For DRF, fewer upper GI events (nausea, vomiting, upper abdominal pain) were reported when assessed by patients and investigators, which is consistent with the hypothesis that DRF may potentially elicit less localized GI irritation compared with DMF, owing to its distinct chemical structure . The potential impact would likely be most evident in the upper GI tract, given that both DRF and DMF are formulated to be released from their capsules and microspheres upon traversing from the stomach into the small intestine; this region of the GI tract would be exposed to the highest concentrations of DRF and DMF, allowing for greater differentiation of their tolerability effects. This was reflected in the worst symptom intensity scores (IGISIS), which show statistically significant differences in favor of DRF for upper GI tract symptoms.
The IGISIS and GGISIS scales were utilized for this study to assess GI symptoms given that evaluation of GI events is not a typical assessment for the management of MS, and no validated scales are currently available to measure such outcomes. As there was no previous experience with the IGISIS and GGISIS scales to inform statistical assumptions, an adaptive trial design was used to enable the selection of a sensitive primary endpoint and inform statistical assumptions for the overall study (see Methods). To mitigate the possibility of a type I error, an analysis to validate the primary endpoint only in patients enrolled after the unblinding (i.e., part B) was included. Results from the part B-only analysis were aligned with that for the overall population on the primary endpoint (46% reduction in the total population; 48% reduction in the part B cohort) as well as secondary endpoints.
Interestingly, the rates of investigator-assessed GI AEs and discontinuations because of GI AEs reported for DRF- and DMF-treated patients were consistent with rates in the ongoing EVOLVE-MS-1 study, as well as with rates in the pivotal DEFINE and CONFIRM studies, though the trials cannot be directly compared [4, 5, 14]. The incidence of flushing, though numerically lower with DRF than DMF in this study, was generally consistent with rates reported in phase III studies with DRF and DMF [4, 5, 14]. However, as the focus of EVOLVE-MS-2 was GI tolerability, we did not evaluate and cannot assess the impact of flushing on patients in the study. There were no unexpected or new safety events, including lymphopenia, reported for patients taking either DRF or DMF, and the overall safety profile was consistent with the known safety profile for each therapy, including interim findings from the ongoing open-label EVOLVE-MS-1 study .
There were limitations of the study. There is potential for bias toward over-reporting when patients self-assess GI events in a study designed to measure GI tolerability using eDiaries three times per day. In this setting, patients were aware via their informed consent that they could potentially receive an investigational product that would reduce GI events, which may have conversely resulted in less reporting overall. Owing to the prospective randomized blinded nature of the study, no bias would have been introduced, although it may have artificially lowered the overall magnitude of difference detected between both arms. The IGISIS and GGISIS scales capture five GI symptoms (nausea, vomiting, upper abdominal pain, lower abdominal pain, and diarrhea) that were most commonly reported in the DEFINE and CONFIRM trials of DMF. However, patients in EVOLVE-MS-2 did experience GI AEs beyond the five included in the IGISIS/GGISIS assessments. Although the scales do not capture every GI AE, the events that are not included occur at low rates (incidence ≤ 2%). Additionally, the short duration of treatment (5 weeks) limits the ability to determine the time of resolution of AEs that were ongoing at the study end, and prohibits the assessment of AEs that occur with a latency. Hence, it does not fully describe the AE profile of DRF and DMF, although this was not the intent of the study. Despite this limited follow-up, the AE profile was consistent with the known profiles for both DRF and DMF, and the high percentage of patients rolling over into the EVOLVE-MS-1 study will allow for the evaluation of the DRF AE profile for up to 2 years on treatment.
In this 5-week head-to-head study evaluating the GI tolerability of DRF vs DMF in patients with RRMS, DRF-treated patients assessed their GI events as less severe and lasting fewer days when compared with patients treated with DMF. Importantly, rates of GI AEs and rates of discontinuation due to GI AEs were lower for patients treated with DRF. Taken together, these findings indicate that DRF has an improved GI tolerability profile compared with DMF, which may lead to better long-term adherence and persistence to therapy.
Data Availability Statement
EVOLVE-MS-2 was registered with ClinicalTrials.gov (NCT03093324). Study data will be shared in accordance with applicable regulations and laws.
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The authors thank Jordan Messer, PharmD, Narinder Nangia, PhD, Yue Cui, PhD, and Mary-Kathryn Canning, MBA for their contributions to this manuscript. Biogen provided funding for medical writing support in the development of this manuscript. Susan Chow, PhD, from Excel Scientific Solutions wrote sections of the first draft of the manuscript based on input from authors, and Miranda Dixon from Excel Scientific Solutions copyedited and styled the manuscript per journal requirements. The authors had full editorial control of the manuscript and provided their final approval of all content.
This study was funded by Alkermes Inc. (Waltham, MA, USA) and Biogen (Cambridge, MA, USA). The open access fee was funded by Biogen.
Conflict of interest
Robert T. Naismith received compensation as an advisor, consultant, or speaker for Alexion, Alkermes, Biogen, Celgene, EMD Serono, Genentech, Novartis, Sanofi Genzyme, TG Therapeutics, and Viela Bio. Annette Wundes received research support from AbbVie, Alkermes, and Biogen, and compensation as an advisor from Biogen. Tiaf Ziemssen received fees for participation in scientific advisory boards from Bayer, Biogen Idec, Sanofi Genzyme, Merck Serono, Novartis, Synthon, and Teva; speaker honorarium from Almirall, Bayer, Biogen, GlaxoSmithKline, Merck Sharp & Dohme, Novartis, Sanofi Genzyme, and Teva; and research support from Bayer, Biogen, Novartis, Sanofi Genzyme, and Teva. Elzbieta Jasinska received fees for participation in scientific advisory boards from Biogen and speaker honoraria from Adamed, Allergan, Hoffman-La Roche, Krka, Novartis, Polpharma, and Teva. Mark S. Freedman received research or educational grants from Genzyme Canada; honoraria or consultation fees from Actelion, Bayer, Biogen, Celgene, Chugai, EMD Serono Canada, Hoffman-La Roche, Merck Serono, Novartis, PendoPharm, Sanofi-Aventis, and Sanofi Genzyme; participated as a member in a company advisory board, board of directors, or other similar group for Actelion, Bayer, Biogen, Clene, Hoffman-La Roche, MedDay, Merck Serono, Novartis, and Sanofi-Aventis; and served on a company-sponsored speaker’s bureau for Sanofi Genzyme. Anthony J. Lembo received fees for participation in scientific advisory boards from Bayer, Biogen Idec, Ironwood, Salix, Shire, and Takeda. Krzysztof Selmaj received consulting fees from Genzyme, Novartis, Ono, Roche, Synthon, and Teva, and speaker fees from Biogen. Ilda Bidollari, Richard Leigh-Pemberton, Maria Lopez-Bresnahan, and David Rezendes are employees of and hold stock/stock options in Alkermes. Hailu Chen, Jerome Hanna, Jennifer Lyons, and Catherine Miller are employees of and hold stock/stock options in Biogen. Jerry S. Wolinsky received compensation for consulting, scientific advisory boards, or other activities with AbbVie, Acorda Therapeutics, Alkermes, Brain Cell Therapeutics, Celgene (Exp 11 2019), Clene Nanomedicine, EMD Serono, Forward Pharma, GeNeuro, GW Pharma, MedDay Pharmaceuticals, NervGen Pharma Corp., Novartis, Otsuka, PTC Therapeutics, Roche/Genentech, and Sanofi Genzyme; compensation for CME activities with AcademicCME, PlatformQ Health Education, PRIME, and Strategic Consultants Intl.; and royalties for out-licensed monoclonal antibodies through UTHealth from Millipore Corporation.
The study was approved by central and local ethics committees and conducted in accordance with the International Council on Harmonisation Guidelines for Good Clinical Practice and the Declaration of Helsinki.
Consent to participate
All patients in EVOLVE-MS-2 provided written informed consent prior to study participation.
Maria Lopez-Bresnahan and David Rezendes: Employees of Alkermes Inc. during the time the research and analyses were conducted.
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Naismith, R.T., Wundes, A., Ziemssen, T. et al. Diroximel Fumarate Demonstrates an Improved Gastrointestinal Tolerability Profile Compared with Dimethyl Fumarate in Patients with Relapsing–Remitting Multiple Sclerosis: Results from the Randomized, Double-Blind, Phase III EVOLVE-MS-2 Study. CNS Drugs 34, 185–196 (2020). https://doi.org/10.1007/s40263-020-00700-0