Solid Performance Supports Sales Growth for Roche

The strong performance was partly due to pandemic headwinds in the second quarter of 2020 creating weaker comparisons.

Securities In This Article
Roche Holding AG ADR
(RHHBY)

We're maintaining our $59 fair value estimate for Roche RHHBY following strong second-quarter results, with top-line growth of 14%. The strong performance was partly due to pandemic headwinds in the second quarter of 2020 creating weaker comparisons and partly due to strong sales growth for Roche's diagnostics and innovative drugs. Core operating profit was up 4% in constant currency in the first half versus sales growth of 8%, due to a higher contribution from the lower-margin diagnostics arm as well as increased investment in pharma R&D. Roche continues to re-route its investment from sales and marketing and into R&D, with 19% growth in R&D expenses in the first half of 2021 for the pharma division, which we think bodes well for Roche's long-term competitive advantages. Roche confirmed its guidance for the full year of low- to mid-single-digit constant currency top-line growth and core earnings per share growth in line with sales growth. We think Roche's combination of branded drugs and diagnostics continues to support a wide moat.

There are several upcoming pipeline updates that could have a significant impact on our fair value estimate. First, Roche expects data in the third quarter for hematology drug Polivy in first-line DLBCL, which we think could allow total Polivy sales north of $2 billion (we model total sales of $1.7 billion by 2030). In 2022, we expect phase 3 data for Alzheimer's drug gantenerumab, which could allow Roche to compete with a cleaner data set than Biogen as well as more convenient subcutaneous dosing. We include a 20% probability of $3 billion in gantenerumab sales by 2030. Roche's SERD (breast cancer) and TIGIT (oncology) will also have pivotal data in 2022 and have potential for blockbuster sales. We expect Roche's newer approved therapies and solid pipeline will drive growth despite continued biosimilar pressure as well as potential new biosimilar launches for opthalmology drug Lucentis (2021) and immunology drug Actemra (2022).

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About the Author

Karen Andersen, CFA

Strategist
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Karen Andersen, CFA, is a sector director, AM Healthcare, for Morningstar*. In addition to leading the sector team, she covers biopharma firms in the US and Europe, focusing mostly on large-cap firms with foundations in biologic or gene-based medicines.

Before joining Morningstar in 2005, Andersen received a master’s degree in business administration from the Jones Graduate School of Business at Rice University, where she served as senior healthcare analyst for the M.A. Wright Fund and earned the distinction of Jones Scholar. She also holds the Chartered Financial Analyst® designation.

She ranked first in the biotechnology industry, and had the highest score overall, in The Wall Street Journal’s annual “Best on the Street” analysts survey in 2013, the last year the survey was conducted.

Andersen holds a bachelor’s degree in biochemistry from Rice University, where she graduated magna cum laude. She is also a member of Phi Beta Kappa. She has scientific research experience in academia at both Rice University and the University of Queensland in Australia. She also worked in the healthcare industry, both at genetic testing firm Integrated Genetics (now part of LabCorp) and as a research assistant at Lexicon Genetics (now Lexicon Pharmaceuticals).

* Morningstar Research Services LLC (“Morningstar”) is a wholly owned subsidiary of Morningstar, Inc

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