Skip to main content
Log in

Lack of Interaction Between Pizotifen and the Novel Antimigraine Compound Zolmitriptan in Healthy Volunteers

  • Drug Interactions
  • Published:
Clinical Drug Investigation Aims and scope Submit manuscript

Summary

This double-blind, randomised, two-period crossover study investigated the effect of pizotifen on the pharmacokinetics and tolerability profile of zolmitriptan (formerly 311C90), a novel selective 5-HT1D receptor agonist for acute migraine therapy. 13 healthy volunteers (mean age 31 years, range 19 to 41 years; mean weight 75kg, range 62 to 89kg) received oral pizotifen 1.5mg or placebo once daily for 8 days with a washout period of at least 2 weeks between study periods. Oral zolmitriptan 10mg was administered with the final dose of pizotifen or placebo. Pizotifen did not significantly affect the pharmacokinetic parameters of zolmitriptan, although in 4 subjects the time to peak plasma zolmitriptan concentration (tmax) was increased in the presence of pizotifen (median increase 1.4 hours). Zolmitriptan caused a small, transient, clinically insignificant increase in blood pressure, which was not affected by pizotifen. No clinically relevant changes in heart rate or 12-lead ECGs were observed. One volunteer was withdrawn because of a brief, 5-beat run, asymptomatic episode of ventricular tachycardia 170 minutes after administration with zolmitriptan plus placebo; this was not considered related to the treatment. Zolmitriptan was well tolerated both alone and in combination with pizotifen. Thus, there is no contraindication to the use of zolmitriptan nor a need for dosage modification in patients concomitantly receiving pizotifen.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Martin GR. Inhibition of the trigemino-vascular system with 5-HT1D agonist drugs: selectively targeting additional sites of action. Eur Neurol 1996; 36 Suppl. 2: 13–8

    Article  PubMed  CAS  Google Scholar 

  2. Dahlöf C, Diener HC, Goadsby PJ, et al. A multicentre double-blind, placebo-controlled, dose range finding study to investigate the efficacy and safety of oral doses of 311C90 in the acute treatment of migraine. Headache 1995; 35: 292

    Google Scholar 

  3. Ferrari MD. The clinical effectiveness of 311C90 in the acute treatment of migraine. Eur Neurol 1996; 36 Suppl. 2: 4–7

    Article  PubMed  CAS  Google Scholar 

  4. Visser WH, Klein KB, Cox RC, et al. 311C90, a new central and peripherally acting 5-HT1D receptor agonist in the acute oral treatment of migraine: a double-blind, placebo-controlled, dose range finding study. Neurology 1996; 46: 522–6

    Article  PubMed  CAS  Google Scholar 

  5. Lance J. Treatment of migraine. Lancet 1992; 339: 1207–9

    Article  PubMed  CAS  Google Scholar 

  6. Speight TM, Avery GS. Pizotifen (BC-105): a review of its pharmacological properties and its therapeutic efficacy in vascular headaches. Drugs 1972; 3: 159–203

    Article  PubMed  CAS  Google Scholar 

  7. Capildeo R, Rose FC. Single-dose pizotifen, 1.5mg nocte: a new approach in the prophylaxis of migraine. Headache 1982; 22: 272–5

    Article  PubMed  CAS  Google Scholar 

  8. Dixon R, Gillotin C, Gibbens M, et al. The pharmacokinetics and effects of blood pressure of multiple doses of the novel antimigraine drug zolmitriptan (311C90) in healthy volunteers. Br J Clin Pharmacol 1997; 43: 273–81

    Article  PubMed  CAS  Google Scholar 

  9. Koch GG. The use of non-parametric methods in the statistical analysis of the 2-period crossover design. Biometrics 1972; 28: 577–84

    Article  PubMed  CAS  Google Scholar 

  10. Seaber E, On N, Dixon R, et al. The absolute bioavailability and metabolic disposition of the novel anti-migraine compound zolmitriptan. Br J Clin Pharmacol 1997. In press

    Google Scholar 

  11. Giorgi L, Dixon R, Touw K. Cardiovascular safety of the novel antimigraine compound 311C90 [abstract P18]. Cephalalgia 1995; 15 Suppl. 14: 220

    Google Scholar 

  12. Earl NL. Clinical safety of 311C90: aggregated data from patients and volunteers to date. Eur Neurol 1996; 36 Suppl. 2: 8–12

    Article  PubMed  CAS  Google Scholar 

  13. Stinson JC, Pears JS, Williams AJ, et al. Use of 24h ambulatory ECG recordings in the assessment of new chemical entities in healthy volunteers. Br J Clin Pharmacol 1995; 39: 651–6

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Seaber, E.J., Gillotin, C., Mohanlal, R. et al. Lack of Interaction Between Pizotifen and the Novel Antimigraine Compound Zolmitriptan in Healthy Volunteers. Clin. Drug Invest. 14, 221–225 (1997). https://doi.org/10.2165/00044011-199714030-00010

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.2165/00044011-199714030-00010

Keywords

Navigation