- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07398417
Fibromyalgisvar med Esreboxetin Evaluert ved Bruk av en Randomisert Tilbaketrekningsforskningsdesign (FORWARD)
En dobbeltblind, placebokontrollert, randomisert tilbaketrekkingsstudie for å vurdere effektiviteten og sikkerheten til AXS-14 i behandlingen av fibromyalgi
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 fibromyalgia.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
This study is a multi-center trial consisting of a 12-week open-label treatment period (OLP), followed by a 12-week double-blind, placebo-controlled, randomized withdrawal period (DBRWP). During the OLP, subjects receive open-label AXS-14. Subjects achieving treatment response will be randomized into the DBRWP in a 1:1 ratio to either continue on AXS-14 or switch to placebo for up to 12 weeks or until a loss of therapeutic response occurs.
Studietype
Registrering (Antatt)
Fase
- Fase 3
Kontakter og plasseringer
Studiekontakt
- Navn: Study Director
- Telefonnummer: 212-332-5061
- E-post: AXS-14-FM-301@axsome.com
Studiesteder
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Arizona
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Glendale, Arizona, Forente stater, 85308
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Phoenix, Arizona, Forente stater, 85032
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Tucson, Arizona, Forente stater, 85704
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Arkansas
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Little Rock, Arkansas, Forente stater, 72211
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California
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Anaheim, California, Forente stater, 92801
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Oceanside, California, Forente stater, 92056
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Redlands, California, Forente stater, 92374
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Sacramento, California, Forente stater, 95821
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Santa Ana, California, Forente stater, 92705
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Connecticut
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Cromwell, Connecticut, Forente stater, 06416
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Florida
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Hollywood, Florida, Forente stater, 33021
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Jacksonville, Florida, Forente stater, 32256
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Lakeland, Florida, Forente stater, 33803
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Maitland, Florida, Forente stater, 32751
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Orlando, Florida, Forente stater, 32801
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Orlando, Florida, Forente stater, 32832
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Tampa, Florida, Forente stater, 33634
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The Villages, Florida, Forente stater, 32159
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Georgia
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Atlanta, Georgia, Forente stater, 30328
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Atlanta, Georgia, Forente stater, 30329
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Marietta, Georgia, Forente stater, 30060
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Norcross, Georgia, Forente stater, 30092
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Illinois
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Chicago, Illinois, Forente stater, 60634
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Tinley Park, Illinois, Forente stater, 60477
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Kansas
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Kansas City, Kansas, Forente stater, 66160
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Overland Park, Kansas, Forente stater, 66209
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Overland Park, Kansas, Forente stater, 66212
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Kentucky
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Louisville, Kentucky, Forente stater, 40205
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Louisiana
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Prairieville, Louisiana, Forente stater, 70769
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Maryland
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Rockville, Maryland, Forente stater, 20850
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Massachusetts
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Boston, Massachusetts, Forente stater, 02131
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North Dartmouth, Massachusetts, Forente stater, 02747
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Watertown, Massachusetts, Forente stater, 02472
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Missouri
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Hazelwood, Missouri, Forente stater, 63042
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Springfield, Missouri, Forente stater, 65807
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Town and Country, Missouri, Forente stater, 63017
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Nevada
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Las Vegas, Nevada, Forente stater, 89102
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New York
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Brooklyn, New York, Forente stater, 11235
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Hartsdale, New York, Forente stater, 10530
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Williamsville, New York, Forente stater, 14221
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North Carolina
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High Point, North Carolina, Forente stater, 27260
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Ohio
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Huber Heights, Ohio, Forente stater, 45424
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Milford, Ohio, Forente stater, 45150
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Oklahoma
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Tulsa, Oklahoma, Forente stater, 74133
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Pennsylvania
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Duncansville, Pennsylvania, Forente stater, 16635
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Plymouth Meeting, Pennsylvania, Forente stater, 19462
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Rhode Island
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Cranston, Rhode Island, Forente stater, 02920
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South Carolina
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Charleston, South Carolina, Forente stater, 29407
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Tennessee
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Knoxville, Tennessee, Forente stater, 37909
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Memphis, Tennessee, Forente stater, 38119
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Texas
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Austin, Texas, Forente stater, 78731
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Austin, Texas, Forente stater, 78737
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Dallas, Texas, Forente stater, 75251
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Houston, Texas, Forente stater, 77089
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Prosper, Texas, Forente stater, 75078
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San Antonio, Texas, Forente stater, 78240
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The Woodlands, Texas, Forente stater, 77832
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Has a primary diagnosis of fibromyalgia based on the 2016 ACR diagnostic criteria.
- Male or female, ≥18 years of age.
- Provides written informed consent to participate in the study before conducting any study procedures.
Exclusion Criteria:
- Previous participation in a clinical trial with reboxetine or esreboxetine or currently receiving treatment with reboxetine for any condition.
- Unable to comply with study procedures.
- Medically inappropriate for study participation in the opinion of the investigator.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: AXS-14 (esreboxetine)
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AXS-14 tablets taken once daily |
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Placebo komparator: Placebo
• Up to 12 weeks in the randomized double-blind period (if applicable) |
Placebo tablets taken once daily |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Tid fra randomisering til tap av terapeutisk respons
Tidsramme: 12 uker
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12 uker
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Samarbeidspartnere og etterforskere
Sponsor
Publikasjoner og nyttige lenker
Hjelpsomme linker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- AXS-14-FM-301
Plan for individuelle deltakerdata (IPD)
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Legemiddel- og utstyrsinformasjon, studiedokumenter
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