Study of NXN 188 for the Treatment of Migraine With Aura

Phase 2

Completed

• Conditions: Migraine With Aura
• Interventions: Drug: sumatriptan succinate; Drug: placebo; Drug: NXN-188

• Registration Number: NCT00920686
• Lead Sponsor: NeurAxon Inc.

Brief Summary

NXN-188 Dihydrochloride is being developed as an immediate release oral product for the treatment of acute migraine. This study is being conducted to evaluate NXN-188 in subjects with a migraine history of aura.

Detailed Description

This was a multicenter, double-blind, parallel group, active and placebo-controlled, three arm study of a single oral dose of NXN-188 for the treatment of acute migraine headache with aura.

After study eligibility was confirmed, subjects were randomized to NXN-188 600 mg, sumatriptan 100 mg, or placebo in a 1:1:1 ratio. Subjects left the clinic to self-administer the treatment at home at the onset of moderate to severe headache in a suitable dosing environment.

Treatment was not to exceed 42 days from Randomization. If the subject did not have a headache within 42 days of randomization (s)he did not take the study medication and returned it to the site. If the subject experienced a qualifying headache (s)he recorded the symptoms in a diary, dosed with the study drug, and called the IVRS to record assessments all adverse events and to report dosing. If the study drug provided insufficient relief 2 hours post dosing (s)he was permitted to use non-triptan rescue medication recommended by the investigator.

Study Timeline

• Study Start: 2009-06
• Study First Submitted: 2009-06-12
• Study First Submitted QC: 2009-06-12
• Study First Posted: 2009-06-15
• Primary Completion: 2010-03
• Study Completion: 2010-03
• Results First Submitted: 2013-05-08
• Status Verified: 2014-07
• Results First Submitted QC: 2014-07-20
• Last Update Submitted: 2014-07-20
• Results First Posted: 2014-08-11
• Last Update Posted: 2014-08-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 239

Inclusion Criteria

1. Male or female migraineurs between 18 and 65 years old.

2. Subjects must have a headache history of migraine with aura as defined by:

   • Aura consisting of at least one of the following, but no muscle weakness or paralysis:

     • Fully reversible visual symptoms
     • Fully reversible sensory symptoms
     • Fully reversible dysphasia

   • Aura has at least two of the following characteristics:

     • Visual symptoms affecting only one side of the field of vision and/or sensory symptoms affecting only one side of the body
     • At least one aura symptom that develops gradually over more than 5 minutes and/or different aura symptoms occur in succession over more than 5 minutes
     • Each symptom lasts from 5-60 minutes

   • Headache begins during the aura or follows aura within 60 minutes

   • Headache not attributable to another disorder

3. Migraine pain following aura in at least 75% of occurrences

4. Headache frequency of at least 1 migraine attack (with or without aura) per month for the past 3 months but not more than 8 migraines in any 30 day period. Subjects must have at least 1 migraine headache with aura per month

   • Each migraine attack should last at least 4 hours (without treatment) and not longer than 72 hours.

5. At the time of the study migraine, prior to dosing with study medication, the headache severity, as judged and documented by the subject, is either moderate or severe (on a 4-point categorical scale)

6. Body mass index (BMI) range of 18 to 35

7. The subject is in general good health.

   • ALT cannot be above 1.5x upper limit of normal; creatinine and urea must be within normal limits

8. Speak, read, and understand English, French, or Spanish sufficiently to understand the nature of the study, to provide written informed consent, and complete all study assessments

9. The subject is willing and able to comply with all testing requirements defined in the protocol

10. All females will avoid pregnancy at least 10 days before randomization, and up until 3 months after dosing.

11. All subjects/partners must use a double-barrier method of birth control during the study and for 3 months after dosing.

Exclusion Criteria

1. A diagnosis of headaches that is not consistent with migraine with aura.

2. Presence of any risk factors that would preclude the use of triptans:

3. Known allergy or hypersensitivity to triptans or history of any serious side effect with a triptan which would preclude further dosing with a triptan

4. Presence of any clinically significant condition that would preclude study participation, as evaluated by the investigator

5. Pregnancy or lactation

6. History of significant neurological, hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, rheumatologic, autoimmune, or metabolic disease

7. Use of the following if taken for migraine prevention:

   • Cardiovascular drugs (acceptable if reason for use is for treatment of cardiovascular disease and the subject has been on a stable dose for 3 months)
   • Valproate, topiramate, cyproheptadine, montelukast, or botulinum toxin.

8. Use of monoamine oxidase inhibitors within 30 days of randomization

9. Initiation of therapy with SSRIs or SNRIs for depression or other approved indication within 90 days of randomization (subjects on stable dose for >3 months for treatment of depression or other approved indication may be included)

10. Are known to or suspected to be currently abusing alcohol or drugs, or have a history (within the past 12 months) of active alcohol or drug abuse

11. Participation in another drug or biologic study within 30 days of randomization into this study or during participation in this study

12. Subjects who are unable or unwilling, in the opinion of the Investigator, to comply with all study procedures and cooperate fully with study center staff

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
sumatriptan succinate 100 mg	sumatriptan succinate	Sumatriptan, 100 mg, PRN
placebo	placebo	matching, PRN
NXN-188	NXN-188	NXN-188, 600 mg, PRN

Primary Outcome Measures

Name	Time	Method
Time (Hours) to First Use of Rescue Medication	24 hours

Secondary Outcome Measures

Name	Time	Method
Headache Relief and Recurrence (Observed Cases)	2, 4 and up to 24 hours	Headache relief is defined as a ≥ 1-point reduction from baseline in Headache Severity Score. The Headache Severity Score is a four-point scale: 0=no pain; 1 = mild pain; 2 = moderate pain; and 3 = severe pain.; Headache recurrence is defined as any subject that experiences headache relief within 4 hours, who did not use rescue medication, and who experienced a worsening of their headache to moderate or severe within 24 hours following study drug administration.
2 Hours Post Administration - Incidence of Complete Headache Relief, Photophobia, Phonophobia and Nausea	2 hours	Complete headache relief is defined as reduction of headache severity from moderate or severe to absent.; Presence of Photophobia and Phonophobia measured on a 2-point scale: 0 = absent; 1 = present; Nausea was measured on a 4-point scale: 0 = no nausea; 1 = mild nausea; 2 = moderate nausea; 3 = severe nausea
4 Hours Post Administration - Incidence of Complete Headache Relief, Photophobia, Phonophobia and Nausea	4 hours	Complete headache relief is defined as reduction of headache severity from moderate or severe to absent.; Presence of Photophobia and Phonophobia measured on a 2-point scale: 0 = absent; 1 = present; Nausea was measured on a 4-point scale: 0 = no nausea; 1 = mild nausea; 2 = moderate nausea; 3 = severe nausea
24 Hours Post Administration - Incidence of Complete Headache Relief, Photophobia, Phonophobia and Nausea	24 hours	Complete headache relief is defined as reduction of headache severity from moderate or severe to absent.; Presence of Photophobia and Phonophobia measured on a 2-point scale: 0 = absent; 1 = present; Nausea was measured on a 4-point scale: 0 = no nausea; 1 = mild nausea; 2 = moderate nausea; 3 = severe nausea

Trial Locations

Locations (16)

The Research Center of Southern California, LLC; 🇺🇸 Oceanside, California, United States

C. Philip O'Carrroll, MD, Inc.; 🇺🇸 Newport Beach, California, United States

San Francisco Headache Clinic; 🇺🇸 San Francisco, California, United States

Comprehensive Neuroscience, Inc.; 🇺🇸 St. Petersburg, Florida, United States

California Medical Clinic for Headache; 🇺🇸 Santa Monica, California, United States

Michigan Head-Pain and Neurological Institute; 🇺🇸 Ann Arbor, Michigan, United States

Headache Care Center/Clinvest; 🇺🇸 Springfield, Missouri, United States

Mercy Health Research; 🇺🇸 St. Louis, Missouri, United States

Regional Clinical Research, Inc.; 🇺🇸 Endwell, New York, United States

Elkind Headache Center; 🇺🇸 Mount Vernon, New York, United States

Rochester Clinical Research, Inc; 🇺🇸 Rochester, New York, United States

Headache Wellness Center; 🇺🇸 Greensboro, North Carolina, United States

Advanced Clinical Research, Inc.; 🇺🇸 West Jordan, Utah, United States

Coastal Carolina Research Center, Inc; 🇺🇸 Mt. PLeasant, South Carolina, United States

Vince and Associates Clinical Research; 🇺🇸 Overland Park, Kansas, United States

Meridian Clinical Research, LLC; 🇺🇸 Omaha, Nebraska, United States