Superior efficacy of new medicines?
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To provide an overview of and discuss newly authorised medicines with an improved efficacy.
This analysis focussed on new medicines with an improved efficacy based on the results of randomised active control trials. Information on comparative efficacy was obtained from the European Medicines Agency European Public Assessment Reports.
Between 1999 and 2005 we identified 122 new medicines with a new active substance. Of these, 13 (10%) were shown to be superior to already available medicines in terms a statistically significant difference in primary clinical endpoints.
A proven advantage in efficacy at an early stage of drug development is the exception rather than the rule. The absence of evidence demonstrating differences between medicines does not necessarily mean that there are no actual differences. Optimal pharmacotherapy would benefit from more comparative research in the development of new medicines. The results of comparative trials need to be critically evaluated for their specific value in clinical practice. To this end, prescription data may be helpful.
KeywordsAdded therapeutic value Comparative information Market authorisation Randomised active control trials Superiority trials
The ultimate goal of developing new medicines should be an improvement in treatment—namely, the new medicine should provide some additional clinical benefit to patients compared to those currently available [1, 2, 3, 4]. This added therapeutic value may lie in one or any of a number of different properties, such as efficacy, safety, applicability, convenience of administration, among others. Of these, efficacy and safety are considered to be the most important: the new medicine should be more efficacious and/or safer.
Demonstrating any improvement is not an explicit condition for being granted marketing authorisation. Data on quality, efficacy and safety are therefore needed in order to demonstrate a favourable benefit/risk ratio when treating a patient for the claimed therapeutic indication. In this context, placebo controlled trials provide robust evidence [5, 6]. However, in the case of new medicines for which good alternatives are available, the regulatory authorities need to be sure that the possibility has been excluded that patients are treated with a product that is less efficacious or less safe . Files submitted to the regulatory authorities can include studies that demonstrate efficacy by confirming the absence of a difference (equivalence trial) or by showing that the new medicine is no worse than an existing medicine (noninferiority trial). Efficacy can also be demonstrated by showing an improved efficacy compared with a medicine already being used in clinical practice for the same claimed therapeutic indication (superiority trial). It goes without saying that the results of these trials are particularly interesting as they provide information on how new medicines, accurately estimated for their efficacy, contribute to an improvement in treatment options for patients. Unfortunately, statistics on the extent of superior medicines as a result of the marketing authorisation process are scarce.
The aim of this study is to provide an overview of and to discuss newly authorised medicines with an improved efficacy.
This study was an in-depth analysis of data from a previous study on the availability of comparative information on new medicines at the time European market authorisation was granted . We therefore analysed the European Public Assessment Reports (EPARs) of the European Medicines Agency (EMEA) between 1999 and 2005 on new medicines with a new active substance . The analysis focussed on new medicines with an improved efficacy based on randomised active control trials (RaCTs). Data on the RaCTs extracted from the EPARs included therapeutic indication, objective, comparator, design, clinical endpoints, results and the conclusion of the Committee for Medicinal Products for Human Use (CHMP) on comparative efficacy.
New medicines (1999–2005) with an improved efficacy
Prevention of venous thromboembolic events
Diabetes mellitus type 1
Insulin regular human
Diabetes mellitus type 2
Insulin regular human
Peginterferon alfa 2a
Chronic hepatitis C
Interferon alfa 2b Interferon alfa 2a
Peginterferon alfa 2b
Chronic hepatitis C
Interferon alfa 2b
Amfotericin B (conv)
Ideally, claims regarding an added value of a new medicine should be based on the results of comparative trials [3, 10]. However, in a previous study we found that nearly one out of two new medicines had been studied in a randomised active control trial . Further analysis of the data on comparative efficacy revealed that an improvement was demonstrated for only one out of ten new medicines. Despite this small number, the conclusion cannot simply be drawn that advances in pharmacotherapy are restricted to these new medicines. Nevertheless, our results suggest that there is sufficient reason to adopt a critical attitude towards the claims of pharmaceutical companies regarding the added value of their new products.
A number of observations can be made regarding this result. First, our analysis excluded new medicines for which no alternative was available and for which, inevitably, a comparative trial was lacking. However, as such medicines were developed as the first medicinal therapy for life-threatening or serious diseases, such as orphan drugs, they can rightfully be considered to be an improvement in the treatment of patients. Secondly, we only focussed on differences in efficacy and not on properties such as safety, applicability or convenience of administration. The reason for this approach is that main/pivotal trials are particularly used for demonstrating efficacy. Nevertheless, new medicines whose efficacy is equivalent or noninferior may still have advantages in terms of safety. An example of this is tenecteplase, which is used in the treatment of suspected myocardial infarction; based on a study of 17,005 patients, it shows an equivalence comparable to alteplase, but a better safety profile .
Another reason for the small number of innovations is that in terms of being granted market authorisation, the demonstration of advantages is not an objective in itself. Consequently, there is no need or requirement to conduct a trial with such an objective. Moreover, pharmaceutical companies would be taking a substantial risk to do so, as failure to demonstrate superiority over a less expensive existing drug could be a financial disaster. The alternative—that a positive result could be expected to lead to substitution of the comparator—appears to carry less weight.
We should note that whether the 13 medicines in our analysis are really a therapeutic improvement depends on a sound review of all relevant properties, the clinical relevance of the differences and the appropriateness of the comparator. It is always important to meticulously add up all of the advantages and disadvantages. This also applies to the medicines in our study, as least as far as it is possible to assess these medicines using the data in the EPAR. For most studies, the EPAR does not provide the basic details of trial design and results in a uniform fashion.
According the EPAR, the efficacy of bimatoprost and travoprost is superior to that of timolol in the treatment of glaucoma, but the safety profiles of the former are inferior due to a higher frequency of ocular side effects. The trial on tipranavir demonstrated a superior antiviral activity, but also a higher frequency of hepatic events and lipodystrophy. Comparative efficacy is always linked to a specific comparator, therapeutic indication and type of patients. In naive human immunodeficient virus (HIV)-infected patients, emtricitabine was more efficacious than stavudine but less efficacious than lamivudine; in experienced patients, lamivudine and stavudine had equal efficacy. In terms of the appropriateness of the comparator, we can conclude that in this study the choice of the comparator in the trials that demonstrated superiority was in line with recommendations on standard treatment .
Another issue in critical evaluations of demonstrated superiority is the choice of the primary clinical endpoint. A composite endpoint was used for fondaparinux; an analysis of all the endpoint events reveals that the incidence of symptomatic venous thromboembolic events, including pulmonary embolism, was not significantly different between treatment groups [13, 14].
The significant advantages and disadvantages of new medicines may only become evident during the course of time, on the basis of further study and experience. This means that assessing the added value of a new medicine is not a one-off incident but a continuous process that is supported by monitoring usage by means of prescription data.
This study shows and discusses how proven superiority, as shown through well-demonstrated advantages in efficacy at an early stage of drug development, is the exception rather than the rule. The absence of evidence for differences between medicines does not necessarily mean that there are no differences. Insight into differences and similarities between medicines, however small they may be, is important in order to be able to make the right choice for the right patient in clinical practice. Therefore, optimal pharmacotherapy would benefit from more comparative research in the development of new medicines. This study also shows that the results of comparative trials should be critically evaluated in terms of their specific value to clinical practice. To this end, prescription data may be helpful.
The authors have no support or funding to report
The authors have declared that no competing interests exist
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