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Phase 1, randomized, parallel-group, double-blind, placebo-controlled trial to evaluate the effects of erenumab (AMG 334) and concomitant sumatriptan on blood pressure in healthy volunteers.
de Hoon, Jan; Van Hecken, Anne; Vandermeulen, Corinne; Herbots, Marissa; Kubo, Yumi; Lee, Ed; Eisele, Osa; Vargas, Gabriel; Gabriel, Kristin.
Affiliation
  • de Hoon J; 1 Center for Clinical Pharmacology, University Hospitals of Leuven, Leuven, Belgium.
  • Van Hecken A; 1 Center for Clinical Pharmacology, University Hospitals of Leuven, Leuven, Belgium.
  • Vandermeulen C; 1 Center for Clinical Pharmacology, University Hospitals of Leuven, Leuven, Belgium.
  • Herbots M; 1 Center for Clinical Pharmacology, University Hospitals of Leuven, Leuven, Belgium.
  • Kubo Y; 2 Global Biostatistical Science, Amgen, Thousand Oaks, CA, USA.
  • Lee E; 3 Clinical Pharmacology Modeling and Simulation, Amgen, Thousand Oaks, CA, USA.
  • Eisele O; 4 Global Patient Safety, Amgen, Thousand Oaks, CA, USA.
  • Vargas G; 5 Neuroscience Early Development, Amgen, Thousand Oaks, CA, USA.
  • Gabriel K; 5 Neuroscience Early Development, Amgen, Thousand Oaks, CA, USA.
Cephalalgia ; 39(1): 100-110, 2019 01.
Article in En | MEDLINE | ID: mdl-29783863
ABSTRACT

OBJECTIVES:

The aim of this study was to assess the effects of concomitant administration of erenumab and sumatriptan on resting blood pressure, pharmacokinetics, safety, and tolerability in healthy subjects.

METHODS:

In this phase 1, parallel-group, one-way crossover, double-blind, placebo-controlled study, healthy adult subjects were randomized (12) to receive either intravenous placebo and subcutaneous sumatriptan 12 mg (i.e. two 6-mg injections separated by 1 hour) or intravenous erenumab 140 mg and subcutaneous sumatriptan 12 mg. Blood pressure was measured pre-dose and at prespecified times post-dose. The primary endpoint was individual time-weighted averages of mean arterial pressure, measured from 0 hours to 2.5 hours after the first dose of sumatriptan. Pharmacokinetic parameters for sumatriptan were evaluated by calculating geometric mean ratios (erenumab and sumatriptan/placebo and sumatriptan). Adverse events and anti-erenumab antibodies were also evaluated.

RESULTS:

A total of 34 subjects were randomized and included in the analysis. Least squares mean (standard error) time-weighted averages of mean arterial pressure were 87.4 (1.0) mmHg for the placebo and sumatriptan group and 87.4 (1.2) mmHg for the erenumab and sumatriptan group. Mean difference in mean arterial pressure between groups was -0.04 mmHg (90% confidence interval -2.2, 2.1). Geometric mean ratio estimates for maximum plasma concentration of sumatriptan was 0.95 (90% confidence interval 0.82, 1.09), area under the plasma concentration-time curve (AUC) from time 0 to 6 hours was 0.98 (90% confidence interval 0.93, 1.03), and AUC from time 0 to infinity was 1.00 (90% confidence interval 0.96, 1.05). No clinically relevant safety findings for co-administration of sumatriptan and erenumab were identified.

CONCLUSION:

Co-administration of erenumab and sumatriptan had no additional effect on resting blood pressure or on pharmacokinetics of sumatriptan. Trial registration ClinicalTrials.gov, NCT02741310.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Pressure / Sumatriptan / Serotonin 5-HT1 Receptor Agonists / Antibodies, Monoclonal, Humanized / Calcitonin Gene-Related Peptide Receptor Antagonists Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Cephalalgia Year: 2019 Type: Article Affiliation country: Belgium

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Pressure / Sumatriptan / Serotonin 5-HT1 Receptor Agonists / Antibodies, Monoclonal, Humanized / Calcitonin Gene-Related Peptide Receptor Antagonists Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Cephalalgia Year: 2019 Type: Article Affiliation country: Belgium