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A Study to Find Out if the Medicine Called Rimegepant is Safe for Adults in India
AN OPEN-LABEL MULTICENTER STUDY TO EVALUATE THE SAFETY AND TOLERABILITY OF RIMEGEPANT 75 MG ODT FOR ACUTE TREATMENT OF MIGRAINE IN ADULT PARTICIPANTS IN INDIA WITH PREVIOUS INSUFFICIENT RESPONSE TO TRIPTANS
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
The primary objective of this study is to evaluate the safety and tolerability of rimegepant 75 mg ODT. The primary endpoints are Incidence of Treatment-emergent adverse events (TEAEs) and Incidence of Serious adverse events (SAEs)
This is a multicenter, single arm, open label phase IV study to evaluate the safety and tolerability of rimegepant 75 mg ODT for acute treatment of migraine with or without aura in adult migraine patients in India with a previous insufficient response to triptans, which includes: inadequate efficacy from treatment with triptans, intolerance to triptans, or contraindication(s) to triptans.
Approximately 60 participants will be enrolled in the study.
The participants who meet the inclusion exclusion criteria will be enrolled within 28 days of screening visit. The site staff will dispense the study medication ie, a single blister card containing one tablet of rimegepant 75 mg ODT to the participant to be taken for the treatment of subsequent migraine attack within 30 days of the baseline visit. Participants will be required to notify the site by a phone call in the event of a migraine attack and confirm whether the medication was taken. Participants will have a 12-hour window to contact the site following a migraine attack so that the call can be completed within the site's working hours. Following this, participants will receive a telephone call approximately 2 days after taking rimegepant 75 mg ODT, during which any AEs or SAEs will be evaluated. Participant satisfaction will be evaluated using TSQM-9 during post dose phone call. The participant will come for an EOS visit (28-35) days post-dose. Total duration of the study can go up to 93 days including, screening period = up to 28 days treatment window = up to 30 days follow up period = up to 35 days post dose (maximum total = 28 + 30 + 35 = up to 93 days)
Studietype
Inschrijving (Geschat)
Fase
- Fase 4
Contacten en locaties
Studiecontact
- Naam: Pfizer CT.gov Call Center
- Telefoonnummer: 1-800-718-1021
- E-mail: ClinicalTrials.gov_Inquiries@pfizer.com
Studie Locaties
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Karnataka
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Bangalore, Karnataka, Indië, 560060
- Werving
- BGS Global Institute of Medical Sciences
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Mangalore, Karnataka, Indië, 575002
- Werving
- Mallikatta Neuro Centre
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria
Participants are eligible to be included in this study only if all of the following criteria apply:
Age and Reproductive Status:
18 years of age or older who meet the reproductive criteria.
Disease Characteristics:
Participant has at least a 1-year history of migraine (with or without aura) consistent with a diagnosis according to the International Classification of Headache Disorders, 3rd Edition, including the following:
At least 5 attacks fulfilling criteria 1-3:
- Headache attacks lasting 4-72 hours (when untreated or unsuccessfully treated).
Headache has at least 2 of the following 4 characteristics:
- Unilateral location
- Pulsating quality
- Moderate or severe pain intensity
- Aggravation by or causing avoidance of routine physical activity (eg, walking or climbing stairs)
During headache, at least 1 of the following:
-Nausea and/or vomiting
- Photophobia and phonophobia
- Not better accounted for by another ICHD-3 diagnosis.
- Participants experience 4-14 migraine days / month and fewer than 7 non-migraine headache days / month on average and overall, less than 15 days with headache (migraine or non-migraine) per month across the 3 months prior to screening.
- Participants on prophylactic migraine medication (non-CGRP) are permitted to remain on therapy if they have been on a stable dose for at least 3 months prior to screening visit, and the dose is not expected to change during the study.
Participants have previous insufficient response and/or prior intolerance to at least one triptan or documented contraindication to the use of triptan.
- Insufficient response - Previous treatment with one or more triptan has yielded no, unsatisfactory or inconsistent therapeutic effect (eg, recurrent, incomplete relief of migraine related symptoms [including pain, nausea, photophobia, phonophobia etc] at 2 hours post dose, non-sustained relief of migraine related symptoms through 24 hours post dose, etc), after repeated dosing (≥2 attempts) at recommended dose level.
Prior intolerance - treatment with triptan has been interrupted because of an adverse event that made continuation of the drug intolerable for the individual.
-Prior triptan associated overuse headache
-Arrhythmia associated with prior triptan use
-Chest/throat/neck/jaw pain, tightness, pressure or heaviness associated with prior use of triptan
-Gastrointestinal ischemia or peripheral vasospastic reaction associated with prior use of triptan
- Serotonin syndrome associated with prior triptan use
Documented contraindication to triptans -
- Documented hypersensitivity to triptan
- Cardiovascular events, conditions and procedures considered contraindications to the use of triptan medications.
i. Events: Myocardial infractions, prior cardiac arrest, transient ischemic attack, cerebrovascular accident (Intracerebral haemorrhage, intracranial haemorrhage, subarachnoid haemorrhage, ischemic stroke) ii. Conditions: Angina pectoris, coronary artery vasospasm, ischemic coronary artery disease, peripheral artery disease, ischemic bowel disease, cardiac conduction disorders (life threatening arrhythmia/heart block) iii. Procedure: Angioplasty, coronary artery bypass grafting, carotid endarterectomy 3) Uncontrolled hypertension
Exclusion Criteria
Participants are excluded from the study if any of the following criteria apply:
Medical Conditions:
Any medical or psychiatric condition including any active suicidal ideation in the past year or suicidal behavior in the past 5 years or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study.
- PHQ-8 total score ≥15
Suicidal ideation and behavior (one, or more, of the below is exclusionary):
- a positive response to item 1 or 2 of the C-SSRS within 30 days prior to Screening;
- suicidal ideation associated with actual intent and/or a method or plan at any time in their lifetime: any positive response on items 3, 4 or 5 of the C-SSRS;
- any previous lifetime history of suicidal behavior: "Yes" to answer to any of the suicidal behavior items of the C-SSRS.
- Current diagnosis of schizophrenia, bipolar, or borderline personality disorder.
- History of severe drug allergy, including anaphylaxis or known hypersensitivity or intolerance to rimegepant or any of its excipients.
Any of the following:
- History of any trigeminal autonomic cephalalgia (eg. cluster headache, Short-lasting, Unilateral, Neuralgiform headache attacks with Conjunctival injection and Tearing [SUNCT], Short-lasting unilateral neuralgiform headache attacks with cranial autonomic symptoms [SUNA], hemicrania continua, paroxysmal hemicrania).
- Active chronic pain syndrome (such as fibromyalgia, chronic pelvic pain, complex regional pain syndrome [CRPS]); Other pain syndromes (including trigeminal neuralgia), dementia, or significant neurological disorders (other than migraine) that, in the Investigator's opinion, interfere with study assessments of safety.
Prior/Concomitant Therapy:
- Current use of any prohibited concomitant medication(s).
History of use of ergotamine medications or triptans for greater than/equal to 10 days per month on a regular basis for greater than/equal to 3 months, or history of non-narcotic analgesic intake for greater than/equal to 15 days per month for greater than/equal to 3 months (eg, acetaminophen, non-steroidal anti-inflammatory drugs [NSAIDs], gabapentin) for other pain indications.
Prior/Concurrent Clinical Study Experience:
Participation in clinical trial with non-biological investigational agents or interventional treatments (last study visit occurring) within the 30 days or 5 half-lives of investigational drug (whichever is longer) prior to Baseline Visit. Participation in clinical trial with biological investigational agents (last study visit occurring) within 90 days or 5 half-lives (whichever is longer) prior to Baseline Visit. Participation in any other investigational clinical trial while participating in this clinical trial.
Diagnostic Assessments:
ANY of the following findings at the Screening Visit and laboratory tests as assessed by the study-specific laboratory:
- eGFR (using CKD-EPI-Scr-Scys Combined) <30 mL/min/1.73m²
- Total bilirubin >1.5 × ULN (may be repeated once, with fractionation, for confirmation during the Screening Phase, and direct bilirubin >ULN is exclusionary if Gilbert's syndrome is suspected)
- AST (SGOT) or ALT (SGPT) >2.0 × ULN
Other Exclusion Criteria:
- Investigator site staff directly involved in the conduct of the study and their family members, site staff otherwise supervised by the investigator, and sponsor and sponsor delegate employees directly involved in the conduct of the study and their family members.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Ander: Rimegepant 75 mg ODT
Rimegepant 75 mg ODT (1 tablet) PRN at the time of migraine attack
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Rimegepant 75 mg ODT (1 tablet) PRN at the time of migraine attack
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Incidence of Treatment-emergent adverse events (TEAEs)
Tijdsspanne: Up to 28 days
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Up to 28 days
|
|
Incidence of Serious adverse events (SAEs)
Tijdsspanne: up to 28 days
|
up to 28 days
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Incidence of clinically significant vital signs abnormalities
Tijdsspanne: up to 28 days
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up to 28 days
|
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Absolute score on treatment satisfaction questionnaire for medication (TSQM-9) subscales
Tijdsspanne: 2-7 days after taking study drug
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2-7 days after taking study drug
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie directeur: Pfizer CT.gov Call Center, Pfizer
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- C4951088
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
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Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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