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September 09, 2014; 83 (11) Article

Randomized controlled trial of the CGRP receptor antagonist telcagepant for migraine prevention

Tony W. Ho, Kathryn M. Connor, Ying Zhang, Eric Pearlman, Janelle Koppenhaver, Xiaoyin Fan, Christopher Lines, Lars Edvinsson, Peter J. Goadsby, David Michelson
First published August 8, 2014, DOI: https://doi.org/10.1212/WNL.0000000000000771
Tony W. Ho
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Kathryn M. Connor
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Ying Zhang
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Eric Pearlman
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Janelle Koppenhaver
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Xiaoyin Fan
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Christopher Lines
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Lars Edvinsson
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Peter J. Goadsby
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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David Michelson
From Merck & Co., Inc. (T.W.H., K.M.C., Y.Z., J.K., X.F., C.L., D.M.), Whitehouse Station, NJ; Mercer University School of Medicine (E.P.), Savannah, GA; Department of Medicine (L.E.), Institute of Clinical Sciences, Lund University and Lund University Hospital, Sweden; Headache Group (P.J.G.), NHIR–Wellcome Trust Clinical Research Facility, King's College London, UK; and Department of Neurology (P.J.G.), University of California, San Francisco. T.W.H. is currently affiliated with AstraZeneca Pharmaceuticals LP, Wilmington, DE. X.F. is currently affiliated with Elan Corporation, Boston, MA.
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Citation
Randomized controlled trial of the CGRP receptor antagonist telcagepant for migraine prevention
Tony W. Ho, Kathryn M. Connor, Ying Zhang, Eric Pearlman, Janelle Koppenhaver, Xiaoyin Fan, Christopher Lines, Lars Edvinsson, Peter J. Goadsby, David Michelson
Neurology Sep 2014, 83 (11) 958-966; DOI: 10.1212/WNL.0000000000000771

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Abstract

Objective: To evaluate whether the calcitonin gene-related peptide (CGRP) receptor antagonist telcagepant might be effective for migraine prevention.

Methods: In this randomized, double-blind, placebo-controlled, multicenter trial (ClinicalTrials.gov NCT00797667), patients experiencing 3–14 migraine days during a 4-week baseline were randomized to telcagepant 140 mg, telcagepant 280 mg, or placebo twice daily for 12 weeks. Efficacy was assessed by mean monthly headache days and migraine/probable migraine days (headache plus ≥1 associated symptom).

Results: The trial was terminated following a recommendation from the Safety Monitoring Board due to hepatotoxicity concerns. At termination, the planned 660 patients had been randomized, 656 had been treated with ≥1 dose of study medication, and 14 had completed the trial. The mean treatment duration was 48–50 days. Thirteen patients, all in the telcagepant groups, had an alanine aminotransferase (ALT) elevation ≥3× the upper limit of normal and 7 of these also had an aspartate aminotransferase elevation ≥3× the upper limit of normal. Two patients had very high symptomatic transaminase elevations that occurred within 2–6 weeks of treatment initiation and resolved after treatment discontinuation. The originally planned efficacy analysis over 12 weeks was not performed due to limited data at later time points, but there was evidence that telcagepant resulted in a larger reduction from baseline than placebo for mean monthly headache days (month 1: 140 mg = −2.9, 280 mg = −3.1, placebo = −1.7; p < 0.05) and migraine/probable migraine days (month 1: 140 mg = −2.7, 280 mg = −3.0, placebo = −1.6; p < 0.05).

Conclusions: These data suggest a potential role for CGRP receptor antagonism in migraine prophylaxis. However, the observed aminotransferase elevations do not support the use of telcagepant for daily administration.

Classification of evidence: This study provides Class II evidence that in patients with migraine, telcagepant taken daily reduces headache days by 1.4 days per month compared to placebo and causes 2.5% of patients to have elevations of serum ALT levels.

GLOSSARY

ALT=
alanine aminotransferase;
AST=
aspartate aminotransferase;
CGRP=
calcitonin gene-related peptide;
ULN=
upper limit of normal

Footnotes

  • Coinvestigators are listed on the Neurology® Web site at Neurology.org.

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Editorial, page 954

  • Supplemental data at Neurology.org

  • Received December 16, 2013.
  • Accepted in final form May 5, 2014.
  • © 2014 American Academy of Neurology
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