Table 5. Probability of success (attrition rate) and cycle time methodology.
Archetype (N = number
of product candidates used in estimation) |
Functional definition for estimating
attrition rate and cycle time ab |
Other adjustments made to assumptions |
---|---|---|
Simple vaccine (N=247) | All vaccines listed for indications requiring
a simple vaccine based on McKinsey pharmaceutical practice classification; excludes influenza vaccines |
Adjusted preclinical phase probability as per Pronker
et al., 2013 12 |
Complex vaccine (N=409) | All vaccines listed for indications requiring
a complex vaccine based on McKinsey pharmaceutical practice classification |
|
Simple NCE (N=3655) | All NCEs with more than 1 candidates in
Phase III or higher as proxy for validated target |
Adjusted preclinical phase probability of success to
55–65% per McKinsey pharmaceutical practice |
Complex NCE (N=4426) | All NCEs with 1 or 0 candidates in Phase III
or higher as proxy for non-validated target |
|
Innovative NCE
(N=14425) |
All NCEs excluding reformulations | N/A |
Simple drug repurposing
(N=3768) |
All reformulations | N/A |
Complex drug
repurposing (N=3768) |
All reformulations | Adjusted preclinical phase probability of success to
75% per Biovista Inc. Drug Repositioning Factsheet |
Simple biologic (N=4247) | All other biologics not categorized as
complex |
Adjusted preclinical phase probability of success to
76% per KMR Pharmaceutical Benchmarking Forum for large new molecular entities; Assumed same spread between simple and complex probability of success from Pharmaprojects database |
Complex biologic
(N=1440) |
All biologics for pharmacology classes
categorized as complex, including gene therapy, antisense therapy, gene delivery vector, RNA interference, stem cell therapy, cellular therapy, and lytic virus |
All assumptions based on Pharmaprojects database (>60,000 individual assets captured) and McKinsey Attrition Analytics Toolkit unless otherwise noted. All data points are from 2007 to 2014.