Pink Sheet is part of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By



Executive Summary

GLAXO's IMITREX EFFECTIVE IN TREATING 74% OF CLUSTER HEADACHES within 15 minutes of treatment compared with a 26% reduction of cluster headaches in patients receiving placebo, according to a study of Imitrex (sumatriptan) published in the Aug. 1 issue of The New England Journal of Medicine. "Seventy-four percent of the patients had a decrease in the severity of headache when their attacks were treated with [6 mg subcutaneous injection of] sumatriptan, whereas 26% had a decrease when they were given placebo," Karl Ekbom, MD, Karolinska Institute, et al. report. "In addition, more patients were free of pain 15 minutes after the injection of sumatriptan than after the injection of placebo (46% vs. 10%)." Glaxo is seeking approval of injectable Imitrex for treating cluster headaches as well as migraines. An NDA was filed in July 1990 covering both indications. The multicenter study of 39 patients consisted of a randomized, double-blind, placebo-controlled crossover design to assess the efficacy of sumatriptan in combating cluster, or Horton's headaches. Patients received a subcutaneous injection of either 6 mg sumatriptan or placebo upon their first headache attack and then were switched to the other treatment for their second headache, which occurred in the next 24 hours to nine days. In addition to reducing pain in more cluster headache attacks, sumatriptan, a serotonin agonist, also had a positive effect on the duration of attacks: 77% of the sumatriptan-treated attacks were fully resolved within 30 minutes of treatment, while only 33% of the placebo-treated attacks were resolved in that time. Adverse events occurred in 35% of the sumatriptan-treated attacks, versus 26% in the placebo-treated headaches. These events were injection-sight reactions and some neurologic symptoms such as dizziness, tiredness, and hot and cold sensations. No one withdrew from the study due to adverse events. A separate article in the same NEJM issue reviews an investigation of sumatriptan's effectiveness against migraine headaches. Michel Ferrari, MD, University Hospital in Leiden, Netherlands, et al., report that a 6 mg dose of sumatriptan reduced pain levels to either "no pain" or "mild pain" in 72% of patients in 60 minutes, while 25% of those receiving placebo experienced similar pain reduction. The study also concluded that the administration of a second dose of the drug an hour after the first dose "affords little additional benefit." The efficacy results of the Ferrari study mirror the findings of another sumatriptan migraine study that appeared in the June 5 issue of the Journal of the American Medical Association. That study, which was also supported by Glaxo and was similar in design to the Ferrari study, found a reduction in pain one hour after administration of the drug in 70% of patients versus only 22% of patients on placebo. An NEJM editorial, by Neil H. Raskin, MD, University of California-San Francisco School of Medicine, includes a comparison of sumatriptan with dihydroergotamine, DHE-45, an FDA-approved migraine treatment marketed by Sandoz. Raskin states that DHE is also "highly effective in aborting migraine attacks," but acts predominantly on different serotonin receptors than does sumatriptan. DHE has been available since the 1950s, but until recently, has not been actively promoted by Sandoz. Due to what the company describes as an "increased awareness of headache," Sandoz "began to consider relaunching DHE some time in the last two years." That effort included a recently released "update" with articles reviewing the product's effectiveness. Sandoz filed an NDA in December 1990 for a nasal spray formulation of DHE.

You may also be interested in...

Part D Discount Liability Coming Into Focus: CMS Releases Drug Cost Data

Newly released Medicare Part D data sheds light on the sales hit that branded pharmaceutical manufacturers will face when the coverage gap discount program gets under way in 2011

FDA Skin Infections Guidance Spurs Debate On Endpoint Relevance

FDA appears headed for a showdown with clinicians and the pharmaceutical industry over the proposed new clinical trial endpoints for acute bacterial skin and skin structure infections, the guidance's approach for justifying a non-inferiority margin and proposed changes in the types of patients that should be enrolled in trials

Shire Hopes To Sow Future Deals With $50M Venture Fund

Specialty drug maker Shire has quietly begun scouting deals with a brand-new $50 million venture fund, the latest of several in-house investment arms to launch with their parent company's pipelines, not profits, as the measure of their worth




Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts