Tämä sivu käännettiin automaattisesti, eikä käännösten tarkkuutta voida taata. Katso englanninkielinen versio lähdetekstiä varten.

A Phase II Study of NB001 for Acute Migraine Treatment (Channel)

tiistai 5. toukokuuta 2026 päivittänyt: 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.

Tutkimuksen yleiskatsaus

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

120

Vaihe

  • Vaihe 2

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

Tutki yhteystietojen varmuuskopiointi

  • Nimi: Mingjie Zhang, Doctor
  • Puhelinnumero: +8618910276582
  • Sähköposti: mjzhangnk@163.com

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen
  • Vanhempi Aikuinen

Hyväksyy terveitä vapaaehtoisia

Ei

Kuvaus

Inclusion Criteria:

  1. The patient is aged ≥18 and ≤65 years at the Screening Visit, of either sex.
  2. 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.
  3. 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.
  4. 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.
  5. According to the investigator's judgment, the patient's untreated or unsuccessfully treated migraine attacks typically last 4 to 72 hours.
  6. The patient is able to read and understand the Informed Consent Form, and signed the Informed Consent Form.
  7. Women of childbearing potential and male participants must practice strict contraception from screening until 30 days after the last dose.
  8. The patient is capable of adequately understanding and completing the study-related scales and using the electronic patient-reported outcome software.

Exclusion Criteria:

  1. 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.
  2. The patient is unable to distinguish migraine attacks from tension-type headaches or other headaches.
  3. 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.
  4. The patient has special types of migraine, such as hemiplegic migraine or migraine with brainstem aura.
  5. The patient has other complex pain syndromes, complex psychiatric disorders, dementia, epilepsy, or other significant neurological disorders as judged by the investigator.
  6. The patient has a chronic, non-headache pain condition requiring daily pain medication.
  7. The patient has clinically significant cardiovascular, cerebrovascular, hematological, endocrine, pulmonary, renal, hepatic, gastrointestinal, psychiatric, or neurological disorders.
  8. 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.
  9. 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.
  10. The patient has active peptic ulcers, chronic gastrointestinal inflammation, or severe hemorrhoids (Grade III-IV internal hemorrhoids or bleeding external hemorrhoids).
  11. 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.
  12. 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.
  13. The patient has a 12-lead ECG result at the Screening Visit showing QTcF >450 msec in males or >470 msec in females.
  14. The patient has a suspected or confirmed history of alcohol or drug abuse.
  15. The patient has a positive pregnancy test, is pregnant or breastfeeding, or is planning to become pregnant.
  16. The patient has participated in another clinical trial within 1 month prior to the Screening Visit.
  17. Subjects deemed by the investigator as inappropriate for enrollment in this clinical study.

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Nelinkertaistaa

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: 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.
Kokeellinen: 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.
Kokeellinen: Four tablets of NB001
Take 4 tablets of NB001 at the onset of moderate-to-severe acute migraine.
Placebo Comparator: Four tablets of placebo
Take 4 tablets of placebo at the onset of moderate-to-severe acute migraine.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Primary Outcome Measure
Aikaikkuna: 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

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Proportion of Subjects with Pain Relief from Baseline at 2 Hours Post-Dose
Aikaikkuna: 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
Aikaikkuna: 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.
Aikaikkuna: 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
Aikaikkuna: 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.
Aikaikkuna: 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
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.

Muut tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Proportion with pain free at each post-dose time points.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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.
Aikaikkuna: 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

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Arvioitu)

Maanantai 20. huhtikuuta 2026

Ensisijainen valmistuminen (Arvioitu)

Keskiviikko 30. syyskuuta 2026

Opintojen valmistuminen (Arvioitu)

Torstai 31. joulukuuta 2026

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Tiistai 7. huhtikuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Tiistai 5. toukokuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Maanantai 11. toukokuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Maanantai 11. toukokuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Tiistai 5. toukokuuta 2026

Viimeksi vahvistettu

Perjantai 1. toukokuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

PÄÄTTÄMÄTÖN

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .

Tilaa