- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07577050
A Phase II Study of NB001 for Acute Migraine Treatment (Channel)
5. mai 2026 oppdatert av: Zhao Dong, MD, Chinese PLA General Hospital
A Phase II, Interventional, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy and Safety of NB001 for the Acute Treatment of Migraine
The goal of this observational study is to Evaluate the Efficacy and Safety of NB001 for the Acute Treatment of Migraine in Adult patients diagnosed with migraine.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Studietype
Intervensjonell
Registrering (Antatt)
120
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Zhao Dong, Doctor
- Telefonnummer: +8618910685535
- E-post: dong_zhaozhao@126.com
Studer Kontakt Backup
- Navn: Mingjie Zhang, Doctor
- Telefonnummer: +8618910276582
- E-post: mjzhangnk@163.com
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
Inclusion Criteria:
- The patient is aged ≥18 and ≤65 years at the Screening Visit, of either sex.
- The patient has a diagnosis of migraine with aura or migraine without aura as defined by the ICHD-3 criteria confirmed at the Screening Visit.
- The patient has had an onset of migraine at <50 years of age, with a history of migraine (with or without aura) of at least 1 year prior to the Screening Visit.
- According to the investigator's judgment, the patient has had 2 to 8 moderate or severe migraine attacks per month in the 3 months prior to the Screening Visit.
- According to the investigator's judgment, the patient's untreated or unsuccessfully treated migraine attacks typically last 4 to 72 hours.
- The patient is able to read and understand the Informed Consent Form, and signed the Informed Consent Form.
- Women of childbearing potential and male participants must practice strict contraception from screening until 30 days after the last dose.
- The patient is capable of adequately understanding and completing the study-related scales and using the electronic patient-reported outcome software.
Exclusion Criteria:
- The patient has a severe allergic constitution, or has known or suspected allergies to the investigational product or its excipients as judged by the investigator.
- The patient is unable to distinguish migraine attacks from tension-type headaches or other headaches.
- The patient has an average history of ≥15 headache days per month in the 3 months prior to the Screening Visit, or currently meets the ICHD-3 diagnostic criteria for chronic migraine, as judged by the investigator.
- The patient has special types of migraine, such as hemiplegic migraine or migraine with brainstem aura.
- The patient has other complex pain syndromes, complex psychiatric disorders, dementia, epilepsy, or other significant neurological disorders as judged by the investigator.
- The patient has a chronic, non-headache pain condition requiring daily pain medication.
- The patient has clinically significant cardiovascular, cerebrovascular, hematological, endocrine, pulmonary, renal, hepatic, gastrointestinal, psychiatric, or neurological disorders.
- The patient has a history of malignancy within 5 years prior to the Screening Visit, with the exception of adequately treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix.
- The patient has any prior history of gastrointestinal disease that may affect the absorption or metabolism of the study drug, or has a recent history of diarrhea.
- The patient has active peptic ulcers, chronic gastrointestinal inflammation, or severe hemorrhoids (Grade III-IV internal hemorrhoids or bleeding external hemorrhoids).
- The patient has tested positive for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibodies, Treponema pallidum antibodies (TPHA), or human immunodeficiency virus (HIV) antibodies at the Screening Visit.
- The patient has hepatic dysfunction: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥1.5 × upper limit of normal; estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m² (calculated using the simplified MDRD formula); or creatine kinase >2.0 × ULN.
- The patient has a 12-lead ECG result at the Screening Visit showing QTcF >450 msec in males or >470 msec in females.
- The patient has a suspected or confirmed history of alcohol or drug abuse.
- The patient has a positive pregnancy test, is pregnant or breastfeeding, or is planning to become pregnant.
- The patient has participated in another clinical trial within 1 month prior to the Screening Visit.
- Subjects deemed by the investigator as inappropriate for enrollment in this clinical study.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: One tablet of NB001 plus three tablets of placebo
|
Take 1 tablet of NB001 + 3 tablets of placebo at the onset of moderate-to-severe acute migraine.
|
|
Eksperimentell: Two tablets of NB001 plus two tablets of placebo
|
Take 2 tablets of NB001 plus 2 tablets of placebo at the onset of moderate-to-severe acute migraine.
|
|
Eksperimentell: Four tablets of NB001
|
Take 4 tablets of NB001 at the onset of moderate-to-severe acute migraine.
|
|
Placebo komparator: Four tablets of placebo
|
Take 4 tablets of placebo at the onset of moderate-to-severe acute migraine.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Primary Outcome Measure
Tidsramme: 2 hours post-dose
|
1.Proportion of subjects with no pain at 2 hours post-dose; 2.proportion of subjects with no most bothersome symptom (MBS) at 2 hours post-dose.
|
2 hours post-dose
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Proportion of Subjects with Pain Relief from Baseline at 2 Hours Post-Dose
Tidsramme: 2 hours post-dose
|
Proportion of subjects with pain relief (defined as reduction from moderate/severe migraine-like headache at baseline [pre-dose] to mild headache or no headache) at 2 hours post-dose.
|
2 hours post-dose
|
|
Restoration of Normal Function at 2 Hours
Tidsramme: 2 hours post-dose.
|
Proportion of subjects with restoration of normal function (as reported by the Functional Disability Scale) at 2 hours post-dose.
|
2 hours post-dose.
|
|
Proportion of subjects using rescue medication within 24 hours post-dose.
Tidsramme: Within 24 hours post-dose.
|
Proportion of subjects using rescue medication within 24 hours post-dose.
|
Within 24 hours post-dose.
|
|
Proportion of subjects with sustained pain relief between 2 and 24 Hours Post-Dose
Tidsramme: Between 2 and 24 hours post-dose.
|
Proportion of subjects with sustained pain relief (defined as pain relief at 2 hours post-dose, no use of rescue medication, and no moderate/severe headache between 2 and 24 hours) between 2 and 24 hours post-dose.
|
Between 2 and 24 hours post-dose.
|
|
Proportion of subjects with sustained pain relief between 2 and 48 hours post-dose.
Tidsramme: Between 2 and 48 hours post-dose.
|
Proportion of subjects with sustained pain relief between 2 and 48 hours post-dose.
|
Between 2 and 48 hours post-dose.
|
|
Proportion of subjects with sustained pain-free status between 2 and 24 Hours Post-Dose
Tidsramme: Between 2 and 24 Hours Post-Dose
|
Proportion of subjects with sustained pain-free status (defined as pain-free at 2 hours post-dose, no use of rescue medication, and no mild/moderate/severe headache between 2 and 24 hours) between 2 and 24 hours post-dose.
|
Between 2 and 24 Hours Post-Dose
|
|
Proportion of subjects with sustained pain-free status between 2 and 48 hours post-dose.
Tidsramme: Between 2 and 48 hours post-dose.
|
Proportion of subjects with sustained pain-free status between 2 and 48 hours post-dose.
|
Between 2 and 48 hours post-dose.
|
|
Proportion of subjects with pain relief at 15, 30, 45, 60, and 90 minutes post-dose.
Tidsramme: At 15, 30, 45, 60, and 90 minutes post-dose.
|
Proportion of subjects with pain relief at 15, 30, 45, 60, and 90 minutes post-dose.
|
At 15, 30, 45, 60, and 90 minutes post-dose.
|
|
Proportion of subjects without MBS (Migraine-associated Symptoms)at 15, 30, 45, 60, and 90 minutes post-dose.
Tidsramme: At 15, 30, 45, 60, and 90 minutes post-dose.
|
Proportion of subjects without MBS (Migraine-associated Symptoms)at 15, 30, 45, 60, and 90 minutes post-dose.
|
At 15, 30, 45, 60, and 90 minutes post-dose.
|
|
Proportion of subjects with pain-free status at 15, 30, 45, 60, and 90 minutes post-dose.
Tidsramme: At 15, 30, 45, 60, and 90 minutes post-dose.
|
Proportion of subjects with pain-free status at 15, 30, 45, 60, and 90 minutes post-dose.
|
At 15, 30, 45, 60, and 90 minutes post-dose.
|
Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Proportion with pain free at each post-dose time points.
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Proportion of subjects with pain free at all recorded time points after dosing;
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
|
Proportion with pain relief at each post-dose time points.
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Proportion with pain relief at each post-dose time points.
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
|
Proportion with absence of MBS at each post-dose time points.
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Proportion of subjects with no MBS (migraine-associated symptoms) at each post-dose time points.
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
|
Proportion of subjects with restoration of normal function at all post-dose time points.
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Proportion of subjects with restoration of normal function at all post-dose time points.
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
|
Resolution of Baseline Phonophobia at Each Post-Dose Time Point
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Among subjects who reported phonophobia as an MBS (migraine-associated symptoms)at baseline, the percentage of subjects with resolution of this symptom at each post-dose time point.
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
|
Proportion of subjects with resolution of baseline photophobia at each post-dose time point
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Among subjects who reported photophobia as an MBS (migraine-associated symptoms)a at baseline, the percentage of subjects with resolution of this symptom at each post-dose time point.
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
|
Proportion of subjects with resolution of baseline nausea at each post-dose time point.
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Among subjects who reported nausea as an MBS before administration, the proportion of subjects with resolution of this symptom at each time point after administration.
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
|
Proportion of subjects with sustained absence of MBS from 2 to 24 hours post-dose.
Tidsramme: From 2 to 24 hours post-dose.
|
Proportion of subjects with sustained absence of MBS from 2 to 24 hours post-dose.
|
From 2 to 24 hours post-dose.
|
|
Proportion of subjects with sustained absence of MBS from 2 to 48 hours post-dose.
Tidsramme: From 2 to 48 hours post-dose.
|
Proportion of subjects with sustained absence of MBS from 2 to 48 hours post-dose.
|
From 2 to 48 hours post-dose.
|
|
Proportion of subjects with sustained normal functional ability from 2 to 24 hours post-dose.
Tidsramme: From 2 to 24 hours post-dose.
|
Proportion of subjects with sustained normal functional ability from 2 to 24 hours post-dose.
|
From 2 to 24 hours post-dose.
|
|
Proportion of subjects with sustained normal functional ability from 2 to 48 hours post-dose.
Tidsramme: From 2 to 48 hours post-dose.
|
Proportion of subjects with sustained normal functional ability from 2 to 48 hours post-dose.
|
From 2 to 48 hours post-dose.
|
|
Proportion of subjects with overall improvement at all recorded post-dose time points and Patient Global Impression of Change (PGI-C) scores.
Tidsramme: At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Proportion of subjects with overall improvement at all recorded post-dose time points and Patient Global Impression of Change (PGI-C) scores.
|
At 15 minutes, 30 minutes, 45 minutes, 60 minutes, 90 minutes, 2 hours, 3 hours, 4 hours, 6 hours, 24 hours, 48 hours post-dose
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
20. april 2026
Primær fullføring (Antatt)
30. september 2026
Studiet fullført (Antatt)
31. desember 2026
Datoer for studieregistrering
Først innsendt
7. april 2026
Først innsendt som oppfylte QC-kriteriene
5. mai 2026
Først lagt ut (Faktiske)
11. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
11. mai 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
5. mai 2026
Sist bekreftet
1. mai 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- NB001-02-002
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
UBESLUTTE
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .