MCP-Mod (Multiple Comparisons Procedure - Modelling) is an increasingly popular statistical methodology. It can generate superior statistical evidence from Phase II trials with regards to dose selection. The FDA & EMA both recently approved this as fit-for-purpose (FFP).
Update July 2020:
Since its development at Novartis, MCP-Mod promises to devise proof-of-concept and dose-ranging trials with greater evidence and data that can prove critical data for Phase III clinical trial design.
Below is an extract from our webinar Sample Size for Phase II Clinical Trials.
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Uncertainty about the optimal dose to maximize efficacy and to minimize safety risks remains a major stumbling block on pipeline productivity. A study that examined examined the reasons for the delay and denial of FDA approval during the years of 2000 to 2012, found that this uncertainty was the most frequent reason for the FDA to reject first-time marketing applications for new molecular entities (NMEs).
Rejection may require additional trials, which means lost time for that crucial period of patent protection. Of the NMEs that were subsequently resubmitted after a rejection for any reason, the median approval delay was 14.5 months, ranging up to 6.5 years.
Traditionally, the design and analysis of dose-response studies have been divided into two strategies: one based on multiple comparison procedures (MCP) and another based on modeling. These approaches have their drawbacks however.
Bretz et al. (2005) proposed a methodology for dose-finding studies, called MCP-Mod, combining MCP principles with modeling techniques. Their approach provides the flexibility of modeling for dose estimation, while preserving the robustness to model misspecification associated with MCP.
The MCP-Mod approach is efficient in the sense that it uses the available data better than the commonly applied pairwise comparisons.... MCP-Mod represents one tool in the toolbox of the well-informed drug developer.
The European Medicines Agency
In 2016 the FDA determined that the Multiple Comparison Procedure – Modeling (MCP-Mod) statistical approach is fit-for-purpose (FFP). They have stated that ''the methodology is scientifically sound” and “advantageous in that it considers model uncertainty and is efficient in the use of the available data compared to traditional pairwise comparisons.” You can find more information regarding MCP-Mod from the FDA here.
In 2014, the European Medicines Agency (EMA) qualified MCP-Mod as an efficient statistical methodology for design and analysis of phase 2 dose-finding studies under model uncertainty. You can read the EMA committee report here and their MCP-MOD workshop resources here.
The MCP-Mod procedure consists of 5 steps, but divided across two distinct stages. The contract research organization Cros NT has an interesting blog that lists the steps they take when applying MCP-mod to a trial.
Stage 1 - The Trial Design Stage
Stage 2 - The Trial Analysis Stage
Watch our recent webinar for practical examples of MCP-Mod. This webinar explains the theory behind MCP-Mod and how to plan a study using this method using a practical example. To watch a recording of this webinar and download the slides just click the image below.