GLOBAL RESEARCH ARCHIVE
First Read: US Pharmaceuticals & Biotechnology "BIIB/DNLI: LRRK2 misses ..."
Research evidence excerpt
First Read: US Pharmaceuticals & Biotechnology "BIIB/DNLI: LRRK2 misses ..."
Valuation Method and Risk Statement
Industry-specific risks include: (1) underwhelming drug product launches, (2) clinical trial
failure or discontinuation, (3) potential regulatory setback. For valuation, we use PE or EV/
sales multiple methodologies, supported by DCF frameworks.
Large Cap Biopharma: Potential downside risks to large cap biotechs are: (1) political and
geopolitical impacts to healthcare related policies (e.g. pricing, tariff, FDA organizational
changes etc.), (2) similarly, other changes in the US healthcare system, which provides a large
portion of revenues for most biopharmaceuticals companies, (3) disappointing launches or
commercial performance of marketed products, (4) FDA and EMEA regulatory decisions on
clinical candidates or approved products that are both on the market and in clinical
development, (5) potential biogeneric competition in the upcoming years for products that
have lost/will lose patent protection.
Biogen: Our valuation is based on a 1yr forward P/E multiple, supported by a DCF framework.
Upside risks include 1) approval, reimbursement and market uptake of anti-amyloid mAbs, 2)
lower than expected competitor pressure in the MS market, 3) slower than expected Spinraza
decline, and 4) success/approvals of assets in the clinical pipeline. Downside risks include 1)
continued restricted coverage by CMS for anti-amyloid mAbs, 2) increased pricing and/or
competitive pressure across MS, 3) increased competitive pressure on Spinraza, and 4)
discontinuation/failure of assets in the clinical pipeline.
Denali: We value the company using a peak sales multiple applied to probability adjusted
sales across its pipeline programs.
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