An Acute Migraine Factorial Study

NCT ID: NCT06245902

Last Updated: 2024-02-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

92 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-18

Study Completion Date

2018-02-08

Brief Summary

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The study consists of a screening visit, out-patient treatment of a moderate or severe migraine attack with a single dose of the study medication within 8 weeks, and End-of-Study Visit 2-7 days after dosing.

Detailed Description

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Conditions

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Migraine With or Without Aura

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors
Factorial Design

Study Groups

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Naltrexone and Acetaminophen

Patients take one capsule containing naltrexone and one capsule containing acetaminophen together for a qualifying migraine

Group Type EXPERIMENTAL

Naltrexone and Acetaminophen

Intervention Type DRUG

Naltrexone plus acetaminophen

Naltrexon/Acetaminophen-High Capsules

Patient take one capsule containing naltrexone (high dose) and one capsule containing acetaminophen together for a qualifying migraine

Group Type EXPERIMENTAL

Naltrexone and Acetaminophen-High Dose

Intervention Type DRUG

Naltrexon (high dose) plus acetaminophen

Naltrexone Alone Capsules

Patient take one capsule containing naltrexone and one capsule containing placebo together for a qualifying migraine

Group Type ACTIVE_COMPARATOR

Naltrexone Alone (regular dose)

Intervention Type DRUG

Naltrexone Alone plus Placebo

Acetaminophen Alone Capsules

Patient take one capsule containing naltrexone and one capsule containing placebo together for a qualifying migraine

Group Type ACTIVE_COMPARATOR

Acetaminophen Alone

Intervention Type DRUG

Acetaminophen Alone plus Placebo

Placebo Capsules

Patient take two capsule containing placebo together for a qualifying migraine

Group Type PLACEBO_COMPARATOR

Matching Placebo

Intervention Type DRUG

Two Placebo capsules

Interventions

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Naltrexone and Acetaminophen

Naltrexone plus acetaminophen

Intervention Type DRUG

Naltrexone and Acetaminophen-High Dose

Naltrexon (high dose) plus acetaminophen

Intervention Type DRUG

Naltrexone Alone (regular dose)

Naltrexone Alone plus Placebo

Intervention Type DRUG

Acetaminophen Alone

Acetaminophen Alone plus Placebo

Intervention Type DRUG

Matching Placebo

Two Placebo capsules

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Male or female 18 years of age or older.
2. History of migraine with or without aura according to the International Classification of Headache Disorders (ICHD)-3rd edition (beta version) for at least one-year with first migraine prior to age 50.
3. Migraine-associated nausea with ≥half of migraine attacks.
4. 2 - 8 migraines per month in each of the previous 3 months.
5. The patient is able to complete study questionnaires, comply with the study requirements and restrictions, and willing to provide written informed consent and authorize HIPAA.
6. The female patient who is premenopausal or postmenopausal less than 1 year, or have not had surgical sterilization (i.e., tubal ligation, partial or complete hysterectomy) must have a negative urine pregnancy test, be non-lactating, and commit to using adequate and reliable contraception throughout the study (e.g., barrier with additional spermicidal, intra-uterine device, hormonal contraception). The male patient must be surgically sterile or commit to the use of 2 different methods of birth control during the study and for 28 days after taking the study drug.

Exclusion Criteria

1. The patient in the opinion of the investigator, may have medication-overuse headache pain (as defined by ICHD - 3 beta criteria for medication-overuse headache), (analgesic, opioid, ergotamine or triptan overuse) during the 3 months preceding screening.
2. The patient in the opinion of the investigator has chronic migraine (as defined by ICHD - 3 beta criteria for chronic migraine).
3. History of cluster headache or neurologically complicated migraine (hemiplegic, basilar, retinal, ophthalmoplegic migraine).
4. Initiation or change in medications with possible migraine prophylactic effects during 3 months before inclusion into the trial (E.g., calcium channel blockers, tricyclic antidepressants, beta-blockers, selective serotonin re-uptake inhibitors (SSRIs), serotonin-norepinephrine re-uptake inhibitors (SNRIs), or Botox).
5. Any concurrent medical or psychiatric condition, this includes, but is not limited to chronic unstable debilitating diseases, significant renal or hepatic impairment.
6. A history within the previous 3 years of abuse of any drug, prescription, illicit, or alcohol.
7. The Female patient is pregnant or breast-feeding. The Male patient is not practicing 2 different methods of birth control with their partner during the study, and for 28 days after the investigational drug last dose or will not remain abstinent during the study, and for 28 days after the last dose.
8. Use of opiates or barbiturates more than 3 days per month.
9. Known-hypersensitivity reaction to any of the components of the investigational drug.
10. Consumption of analgesic medication for other conditions on a regular basis, (nonsteroidal anti-inflammatory drugs, or acetaminophen, or muscle relaxants).
11. Use of emergency care treatment more than 3 times in the previous 6 months.
12. Participation in another study with an investigational drug within 30 days prior to randomization and/or a plan to participate during the study.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Allodynic Therapeutics, Inc

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Annette C Toledano, M.D.

Role: STUDY_DIRECTOR

Allodynic Therapeutics, Inc

Locations

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Annette C. Toledano MD

North Miami, Florida, United States

Site Status

Countries

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United States

References

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Wang X, Zhang Y, Peng Y, Hutchinson MR, Rice KC, Yin H, Watkins LR. Pharmacological characterization of the opioid inactive isomers (+)-naltrexone and (+)-naloxone as antagonists of toll-like receptor 4. Br J Pharmacol. 2016 Mar;173(5):856-69. doi: 10.1111/bph.13394. Epub 2016 Feb 4.

Reference Type RESULT
PMID: 26603732 (View on PubMed)

Kato J, Svensson CI. Role of extracellular damage-associated molecular pattern molecules (DAMPs) as mediators of persistent pain. Prog Mol Biol Transl Sci. 2015;131:251-79. doi: 10.1016/bs.pmbts.2014.11.014. Epub 2015 Jan 30.

Reference Type RESULT
PMID: 25744676 (View on PubMed)

Lewis SS, Loram LC, Hutchinson MR, Li CM, Zhang Y, Maier SF, Huang Y, Rice KC, Watkins LR. (+)-naloxone, an opioid-inactive toll-like receptor 4 signaling inhibitor, reverses multiple models of chronic neuropathic pain in rats. J Pain. 2012 May;13(5):498-506. doi: 10.1016/j.jpain.2012.02.005. Epub 2012 Apr 20.

Reference Type RESULT
PMID: 22520687 (View on PubMed)

Watkins LR, Hutchinson MR, Ledeboer A, Wieseler-Frank J, Milligan ED, Maier SF. Norman Cousins Lecture. Glia as the "bad guys": implications for improving clinical pain control and the clinical utility of opioids. Brain Behav Immun. 2007 Feb;21(2):131-46. doi: 10.1016/j.bbi.2006.10.011. Epub 2006 Dec 18.

Reference Type RESULT
PMID: 17175134 (View on PubMed)

Hutchinson MR, Zhang Y, Brown K, Coats BD, Shridhar M, Sholar PW, Patel SJ, Crysdale NY, Harrison JA, Maier SF, Rice KC, Watkins LR. Non-stereoselective reversal of neuropathic pain by naloxone and naltrexone: involvement of toll-like receptor 4 (TLR4). Eur J Neurosci. 2008 Jul;28(1):20-9. doi: 10.1111/j.1460-9568.2008.06321.x.

Reference Type RESULT
PMID: 18662331 (View on PubMed)

Wieseler J, Ellis A, McFadden A, Stone K, Brown K, Cady S, Bastos LF, Sprunger D, Rezvani N, Johnson K, Rice KC, Maier SF, Watkins LR. Supradural inflammatory soup in awake and freely moving rats induces facial allodynia that is blocked by putative immune modulators. Brain Res. 2017 Jun 1;1664:87-94. doi: 10.1016/j.brainres.2017.03.011. Epub 2017 Mar 16.

Reference Type RESULT
PMID: 28322750 (View on PubMed)

Su M, Ran Y, He Z, Zhang M, Hu G, Tang W, Zhao D, Yu S. Inhibition of toll-like receptor 4 alleviates hyperalgesia induced by acute dural inflammation in experimental migraine. Mol Pain. 2018 Jan-Dec;14:1744806918754612. doi: 10.1177/1744806918754612. Epub 2018 Jan 8.

Reference Type RESULT
PMID: 29310498 (View on PubMed)

Dewall CN, Macdonald G, Webster GD, Masten CL, Baumeister RF, Powell C, Combs D, Schurtz DR, Stillman TF, Tice DM, Eisenberger NI. Acetaminophen reduces social pain: behavioral and neural evidence. Psychol Sci. 2010 Jul;21(7):931-7. doi: 10.1177/0956797610374741. Epub 2010 Jun 14.

Reference Type RESULT
PMID: 20548058 (View on PubMed)

Younger J, Mackey S. Fibromyalgia symptoms are reduced by low-dose naltrexone: a pilot study. Pain Med. 2009 May-Jun;10(4):663-72. doi: 10.1111/j.1526-4637.2009.00613.x. Epub 2009 Apr 22.

Reference Type RESULT
PMID: 19453963 (View on PubMed)

Lipton RB, Baggish JS, Stewart WF, Codispoti JR, Fu M. Efficacy and safety of acetaminophen in the treatment of migraine: results of a randomized, double-blind, placebo-controlled, population-based study. Arch Intern Med. 2000 Dec 11-25;160(22):3486-92. doi: 10.1001/archinte.160.22.3486.

Reference Type RESULT
PMID: 11112243 (View on PubMed)

Kaki AM, El-Yaski AZ, Youseif E. Identifying neuropathic pain among patients with chronic low-back pain: use of the Leeds Assessment of Neuropathic Symptoms and Signs pain scale. Reg Anesth Pain Med. 2005 Sep-Oct;30(5):422-8. doi: 10.1016/j.rapm.2005.05.013.

Reference Type RESULT
PMID: 16135345 (View on PubMed)

Related Links

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https://search.usa.gov/search?utf8=%E2%9C%93&affiliate=iprcc&query=tlr4&x=0&y=0

2009-2013 Pain Research Advances \| Interagency Pain ...Thus, identifying potential new medications is critical. Recent evidence indicates a pivotal role for the receptor known as toll-like receptor 4 (TLR4 ...

Other Identifiers

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ANODYNE-1 Version 1.3

Identifier Type: -

Identifier Source: org_study_id

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