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

5. Mai 2026 aktualisiert von: 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.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

120

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

  • Name: Mingjie Zhang, Doctor
  • Telefonnummer: +8618910276582
  • E-Mail: mjzhangnk@163.com

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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.
Experimental: 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.
Experimental: 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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Primary Outcome Measure
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Proportion of Subjects with Pain Relief from Baseline at 2 Hours Post-Dose
Zeitfenster: 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
Zeitfenster: 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.
Zeitfenster: 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
Zeitfenster: 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.
Zeitfenster: 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
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Proportion with pain free at each post-dose time points.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

20. April 2026

Primärer Abschluss (Geschätzt)

30. September 2026

Studienabschluss (Geschätzt)

31. Dezember 2026

Studienanmeldedaten

Zuerst eingereicht

7. April 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. Mai 2026

Zuerst gepostet (Tatsächlich)

11. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

11. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

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UNENTSCHIEDEN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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