Literature DB >> 28664660

Unwarranted claims of drug efficacy in pharmaceutical sales visits: are drugs approved on the basis of surrogate outcomes promoted appropriately?

Roojin Habibi1, Joel Lexchin2, Barbara Mintzes3, Anne Holbrook4.   

Abstract

AIMS: This study compares physicians' recall of the claims of benefits on cardiovascular disease and diabetes made by pharmaceutical sales representatives for drugs approved on the basis of a surrogate outcome, i.e., an off-label claim, compared with those approved on the basis of a serious morbidity or mortality (clinical) outcome.
METHODS: Physicians in primary care practices in Montreal, Vancouver, Sacramento and Toulouse, who saw sales representatives as part of their usual practice and served a non-referral population, were contacted in blocks of 25 from a randomized list of all physicians practising in the relevant metropolitan area. We compared how frequently physicians reported that sales reps made claims of serious morbidity or mortality (clinically meaningful) benefits for drugs approved on the basis of surrogate outcomes vs. drugs approved on the basis of clinical outcomes.
RESULTS: There were 448 promotions for 58 unique brand name cardiovascular and diabetes drugs. Claims of clinically meaningful benefit were reported in 156 (45%) of the 347 promotions for surrogate outcome drugs, constituting unwarranted efficacy claims, i.e., off-label promotion. Claims of clinical benefit were reported in 72 of the 101 promotions (71%) for drugs approved on the basis of clinical outcomes, adjusted OR = 0.3 (95% CI 0.2, 0.6), P < 0.001.
CONCLUSIONS: Claims of efficacy made in sales visit promotions for drugs approved only on the basis of surrogate outcomes extended beyond the regulator-approved efficacy information for the product in almost half of promotions. Unapproved claims of drug efficacy constitute a form of off-label promotion and merit greater attention from regulators.
© 2017 The British Pharmacological Society.

Entities:  

Keywords:  clinical outcome; off-label promotion; pharmaceutical promotion; sales representatives; surrogate outcome

Mesh:

Year:  2017        PMID: 28664660      PMCID: PMC5651306          DOI: 10.1111/bcp.13360

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  27 in total

Review 1.  Lessons from the glitazones: a story of drug development.

Authors:  E A Gale
Journal:  Lancet       Date:  2001-06-09       Impact factor: 79.321

2.  Accuracy of pharmaceutical advertisements in medical journals.

Authors:  Pilar Villanueva; Salvador Peiró; Julián Librero; Inmaculada Pereiró
Journal:  Lancet       Date:  2003-01-04       Impact factor: 79.321

3.  Pharmaceutical advertisements in leading medical journals: experts' assessments.

Authors:  M S Wilkes; B H Doblin; M F Shapiro
Journal:  Ann Intern Med       Date:  1992-06-01       Impact factor: 25.391

Review 4.  The Strength of Association Between Surrogate End Points and Survival in Oncology: A Systematic Review of Trial-Level Meta-analyses.

Authors:  Vinay Prasad; Chul Kim; Mauricio Burotto; Andrae Vandross
Journal:  JAMA Intern Med       Date:  2015-08       Impact factor: 21.873

5.  Unwarranted claims of drug efficacy in pharmaceutical sales visits: are drugs approved on the basis of surrogate outcomes promoted appropriately?

Authors:  Roojin Habibi; Joel Lexchin; Barbara Mintzes; Anne Holbrook
Journal:  Br J Clin Pharmacol       Date:  2017-08-19       Impact factor: 4.335

6.  Risk of acute myocardial infarction, stroke, heart failure, and death in elderly Medicare patients treated with rosiglitazone or pioglitazone.

Authors:  David J Graham; Rita Ouellet-Hellstrom; Thomas E MaCurdy; Farzana Ali; Christopher Sholley; Christopher Worrall; Jeffrey A Kelman
Journal:  JAMA       Date:  2010-06-28       Impact factor: 56.272

Review 7.  Information from pharmaceutical companies and the quality, quantity, and cost of physicians' prescribing: a systematic review.

Authors:  Geoffrey K Spurling; Peter R Mansfield; Brett D Montgomery; Joel Lexchin; Jenny Doust; Noordin Othman; Agnes I Vitry
Journal:  PLoS Med       Date:  2010-10-19       Impact factor: 11.069

8.  Medicines information provided by pharmaceutical representatives: a comparative study in Australia and Malaysia.

Authors:  Noordin Othman; Agnes I Vitry; Elizabeth E Roughead; Shaiful B Ismail; Khairani Omar
Journal:  BMC Public Health       Date:  2010-11-30       Impact factor: 3.295

Review 9.  Comparison of treatment effect sizes associated with surrogate and final patient relevant outcomes in randomised controlled trials: meta-epidemiological study.

Authors:  Oriana Ciani; Marc Buyse; Ruth Garside; Toby Pavey; Ken Stein; Jonathan A C Sterne; Rod S Taylor
Journal:  BMJ       Date:  2013-01-29

10.  Surrogate outcomes: experiences at the Common Drug Review.

Authors:  Angela Rocchi; Shoghag Khoudigian; Rob Hopkins; Ron Goeree
Journal:  Cost Eff Resour Alloc       Date:  2013-12-17
View more
  3 in total

1.  Innovation and off-label use, the French case and more.

Authors:  Alain Braillon; Joel Lexchin
Journal:  Br J Clin Pharmacol       Date:  2019-06-04       Impact factor: 4.335

2.  Unwarranted claims of drug efficacy in pharmaceutical sales visits: are drugs approved on the basis of surrogate outcomes promoted appropriately?

Authors:  Roojin Habibi; Joel Lexchin; Barbara Mintzes; Anne Holbrook
Journal:  Br J Clin Pharmacol       Date:  2017-08-19       Impact factor: 4.335

3.  Undergraduate and postgraduate pharmacovigilance education: A proposal for appropriate curriculum content.

Authors:  Raquel Herrera Comoglio
Journal:  Br J Clin Pharmacol       Date:  2020-02-05       Impact factor: 4.335

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.