NeuroNow, a biopharma company, seeks to determine if they should invest in Phase 3 clinical trials for a new oral multiple sclerosis drug. The case requires market sizing (starting with 0.1% MS incidence in a 300M population), projecting oral drug adoption growth, estimating NeuroNow’s market share (40%), and conducting profitability analysis against development costs. The analysis shows breakeven within 1 year of launch in 2021 with $1.9Bn total profit over 5 years, supporting the investment recommendation.
Key Insights:
- Market sizing requires multiple haircuts: population incidence, diagnosis rate, treatment rate, and share of oral vs. injectable modality
- The case leverages Exhibit 1 showing market paradigm shift from injectables (95% in 2015) to orals (90% by 2025), validating growth assumptions
- Market research qualitative data (physician, payer, patient quotes) justifies a 40% market share assumption for NeuroNow given superior safety profile and lower side effects
- Breakeven analysis requires tracking both revenue (patient volume × price × market share) and multi-year cost structure (R&D, launch, salesforce, marketing, manufacturing)
- Key risks include clinical trial failure, competitive response from incumbents, regulatory changes, and supply chain issues that should be explicitly acknowledged