Esreboxetine for Fibromyalgia
(FORWARD Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called esreboxetine to determine its effectiveness in managing fibromyalgia, a condition causing widespread pain and fatigue. Researchers aim to assess the safety and efficacy of this medication compared to a placebo (a pill with no active medicine). Participants will receive either esreboxetine or a placebo for up to 12 weeks. The trial seeks individuals diagnosed with fibromyalgia according to specific criteria set in 2016. As a Phase 3 trial, this treatment represents the final step before FDA approval, offering participants an opportunity to contribute to potentially groundbreaking advancements in fibromyalgia management.
Is there any evidence suggesting that esreboxetine is likely to be safe for humans?
Research has shown that esreboxetine has been tested in several studies for fibromyalgia. In these studies, participants found esreboxetine safe and well-tolerated. The trials compared the drug to a placebo, a non-active substance, to determine its real effects. These studies, lasting between 8 to 14 weeks, did not reveal any major safety concerns for esreboxetine.
It is also important to note that Pfizer chose not to continue its trials with esreboxetine for fibromyalgia, but this decision was not due to safety issues. Current evidence suggests that esreboxetine is generally safe.12345Why do researchers think this study treatment might be promising for fibromyalgia?
Esreboxetine is unique because it targets norepinephrine reuptake, which is a different mechanism compared to most current fibromyalgia treatments that often focus on serotonin levels. This selective norepinephrine reuptake inhibitor (NRI) could offer a fresh approach to managing pain and fatigue, key symptoms of fibromyalgia. Researchers are excited about esreboxetine because it holds the potential to provide relief where other medications, like those targeting serotonin or using anticonvulsants, may fall short.
What evidence suggests that esreboxetine might be an effective treatment for fibromyalgia?
Research has shown that esreboxetine, the treatment under study in this trial, offers promising results for managing fibromyalgia symptoms. Participants may receive esreboxetine, which previous studies have demonstrated leads to significant improvements in pain, daily activities, and tiredness compared to a placebo. One study reported that esreboxetine led to a noticeable decrease in the Fibromyalgia Impact Questionnaire score, measuring fibromyalgia's effect on daily life. Additionally, patients tolerated esreboxetine well, experiencing few side effects. These findings suggest that esreboxetine could be effective for people with fibromyalgia.678910
Are You a Good Fit for This Trial?
This trial is for adults diagnosed with fibromyalgia. Participants should generally be in stable health and able to follow study procedures. People with certain other medical or psychiatric conditions, or those taking conflicting medications, may not be eligible.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Open-label Treatment
Participants receive open-label AXS-14 for fibromyalgia management
Double-blind Randomized Withdrawal
Participants are randomized to continue AXS-14 or switch to placebo to assess efficacy and safety
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Esreboxetine
Trial Overview
The study tests AXS-14 (Esreboxetine), a new medication, against a placebo to see how well it helps manage fibromyalgia symptoms. It uses a randomized withdrawal design where neither patients nor doctors know who gets the real drug.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
* Up to 12 weeks in the open-label period; * Up to 12 weeks in the randomized double-blind period (if applicable)
• Up to 12 weeks in the randomized double-blind period (if applicable)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Axsome Therapeutics, Inc.
Lead Sponsor
Citations
Long-Term Safety and Efficacy of Esreboxetine for ...
Similar improvement trends were reported on the Fibromyalgia Impact Questionnaire (FIQ): mean FIQ decrease was -18.27 at Week 32. These results demonstrate the ...
AXS-14
AXS-14 has met the primary endpoints and demonstrated positive and statistically significant results in a Phase 3 and in a Phase 2 trial for the treatment of ...
Study Details | NCT07398417 | Fibromyalgia Response ...
The study is a Phase 3, double-blind, placebo-controlled, randomized withdrawal study to assess the efficacy and safety of AXS-14 in the management of ...
Safety and efficacy of esreboxetine in patients with ...
Esreboxetine was generally well tolerated and was associated with significant improvements in pain, FIQ, PGIC, and fatigue scores compared with placebo.
5.
psychiatrictimes.com
psychiatrictimes.com/view/first-patient-dose-in-phase-3-trial-of-axs-14-for-treatment-of-fibromyalgiaFirst Patient Dose in Phase 3 Trial of AXS-14 for Treatment ...
AXS-14 is a selective norepinephrine reuptake inhibitor, showing efficacy in improving fibromyalgia symptoms like pain, function, and fatigue.
Esreboxetine 98819-76-2 wiki
Esreboxetine CAS 98819-76-2 WIKI information includes physical and chemical properties, USES, security data, NMR spectroscopy, computational chemical data ...
Mean of Daily Versus Single Week Recall-Based Pain ...
Esreboxetine has demonstrated efficacy and safety in placebo-controlled fibromyalgia trials ranging in duration from 8-14 weeks (Arnold, 2010; Arnold, 2012).
EX-99.1
Fibromyalgia: Axsome is conducting the FORWARD study, a Phase 3, double-blind, placebo-controlled, multicenter, randomized withdrawal trial ...
Last observation carried forward approach... : Arthritis & ...
Safety and efficacy of esreboxetine in patients with fibromyalgia: a fourteen-week, randomized, double-blind, placebo-controlled, multicenter clinical trial.
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trialx.com
trialx.com/clinical-trials/listings/location/united-states/TN/Collierville/?page\u003d9Collierville, Tennessee Clinical Research Trials
Fibromyalgia Response With Esreboxetine Evaluated ... The purpose of this study is to provide efficacy and safety data for remibrutinib in patients with secondary ...
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