Staccato Prochlorperazine in Migraine (Out Patient)

Completed · Phase 2 · Has a placebo group

Conditions studied: Migraine Headache, Aura

In brief

Staccato Prochlorperazine is being developed to treat patients suffering from acute migraine headaches. In October 2005, we completed a 75 patient, multi-center, double-blind placebo-controlled Phase 2A clinical trial in patients suffering from moderate to severe acute migraine headaches. This Phase 2B clinical trial of Staccato Prochlorperazine has been initiated to assess the efficacy and safety in outpatients with migraine headache with or without aura.

Key facts

Study ID

NCT00422812

Run by

Alexza Pharmaceuticals, Inc.

People needed

400

Starts

2006-04-01

Expected to finish

2007-01-01

Last updated by the study team

2018-01-25

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female patients between the ages of 18 to 70 years, inclusive.
• Patients who have migraine headache with or without aura (diagnosis according to International Headache Society guidelines) for at least 6 months.
• Patients who have a history of migraine and have had at least 3 migraine attacks in the last 3 month period (but not more than 8 migraine attacks per month). Current and past migraine medication history must be recorded.
• Patients who agree to: not use the study drug within 72 hr of a prior migraine attack, and to use the investigational medication when they have a pain rating of Moderate or Severe (on a None, Mild, Moderate or Severe Scale) prior to dosing.
• Patients who speak, read, and understand English sufficiently well and are willing and able to provide written informed consent on an IRB approved form prior to the initiation of any study procedures.
• Patients who are willing and able comply with the study schedule and study requirements, and agree to return to the clinic within 5 working days of use of the investigational treatment.
• Patients who are in good general health prior to study participation as determined by a detailed medical history, physical examination, 12-lead ECG, blood chemistry profile, hematology, urinalysis and in the opinion of the Principal Investigator.
• Female participants (if of child-bearing potential and sexually active) and male participants (if sexually active with a partner of child-bearing potential) who agree to use a medically acceptable and effective birth control method throughout the study and for one week following the end of the study. Medically acceptable methods of contraception that may be used by the participant and/or his/her partner include abstinence, birth control pills or patches, diaphragm with spermicide, intrauterine device (IUD), condom with foam or spermicide, vaginal spermicidal suppository, surgical sterilization and progestin implant or injection. Prohibited methods include: the rhythm method, withdrawal, condoms alone, or diaphragm alone.

You may not qualify if…

• Patients who are currently taking tricyclic antidepressants, valproate, divalproex, barbitals, thiazolidinediones, phenothiazines, benzodiazepines, lithium or any hepatic toxic drugs must be excluded.
• Patients who are currently taking medications that prolong the QT/QTc interval (see Appendix 4) must be excluded.
• Patients with a history of contraindications to anticholinergics (bowel obstruction, urinary retention, acute glaucoma) must be excluded.
• Patients with a history of allergy or intolerance to phenothiazines and related drugs (prochlorperazine, chlorpromazine, promethazine, mesoridazine, thioridazine, fluphenazine, perphenazine) must be excluded.
• Patients with a history of extra-pyramidal disorders, movement disorders, neuroleptic malignant syndrome, or major affective disorder must be excluded.
• Female patients who have a positive pregnancy test at screening or are breastfeeding must be excluded.
• Patients who have a history within the past year of drug or alcohol dependence or abuse as defined by DSM-4 must be excluded.
• Patients who have a history of pheochromocytoma, seizure disorder or Parkinson's disease must be excluded.
• Patients who have a history of syncope, unstable angina, myocardial infarction (within 6 mos), congestive heart failure, or transient ischemic attack must be excluded.
• Patients who have a history of a major neurological disorder other than migraine (subarachnoidal bleeding, stroke, brain tumor) must be excluded.
• Patients who have any other disease(s), by history, physical examination, or laboratory abnormalities (ALT or AST > 2-fold the upper limit of normal, Bilirubin > 1.5 mg/dL, or creatinine > 1.8 mg/dL) or that in the investigator's opinion, would present undue risk to the patient or may confound the interpretation of study results must be excluded.
• Patients who have a history of asthma or chronic obstructive lung disease should be excluded.
• Patients who have received an investigational drug within 30 days prior to the Screening Visit must be excluded.
• Patients who have a history of risk factors for Torsade de Pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome) must be excluded.
• Patients who have a marked prolongation of QT/QTc interval (e.g., demonstration of a QT interval >450 ms on screening ECG) must be excluded.
• Patients who are considered by the investigator, for any reason, to be an unsuitable candidate for receiving prochlorperazine, or unable to use the inhalation device, must be excluded.

Where it is running

• Department of Neurology, Mayo Clinic — Scottsdale, Arizona, United States
• San Francisco Headache Clinic — San Francisco, California, United States
• California Medical Clinic for Headache — Santa Monica, California, United States
• Neurological Research Institute of East Bay — Walnut Creek, California, United States
• Mile High Research Center — Denver, Colorado, United States
• Associated Neurologists of Southern Connecticut PC — Fairfield, Connecticut, United States
• Hartford Headache Center — Hartford, Connecticut, United States
• The New England Center for Headache — Stamford, Connecticut, United States
• MD Clinical — Hallandale, Florida, United States
• Palm Beach Neurological Center — West Palm Beach, Florida, United States
• Diamond Headache Clinic — Chicago, Illinois, United States
• Medvadis — Wellesley Hills, Massachusetts, United States
• New England Regional Headache Center — Worcester, Massachusetts, United States
• The Michigan Head-Pain and Neurological Institute — Ann Arbor, Michigan, United States
• Headache Care Center Primary Care Network, INC — Springfield, Missouri, United States
• Regional Clinical Research — Endwell, New York, United States
• Elkind Headache Center — Mount Vernon, New York, United States
• New York Headache Center — New York, New York, United States
• Island Neurological Associates, PC — Plainview, New York, United States
• PharmQuest — Greensboro, North Carolina, United States
• Health Research Associates — Cleveland, Ohio, United States
• ClinExcel Research — West Chester, Ohio, United States
• University Neurologists/OUHSC — Oklahoma City, Oklahoma, United States
• Houston Headache Clinic — Houston, Texas, United States
• Swedish Research Center — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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