Maintaining Our Moderna FVE Amid Lower Vaccine Guidance

We're maintaining our fair value estimate for Moderna following disappointing third-quarter results and updated COVID-19 vaccine sales guidance.

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Moderna Inc
(MRNA)

We're maintaining our $158 fair value estimate for Moderna MRNA following disappointing third-quarter results and updated COVID-19 vaccine sales guidance. Moderna sold 208 million COVID-19 vaccine doses in the third quarter for $4.8 billion, lower than our $7 billion estimate for the quarter, due to a combination of dose release bottlenecks, greater complexity of distribution to more global markets, and lower average global pricing (as more vaccine is delivered to less-developed countries). While some of these sales will be pushed into the fourth quarter or early 2022, we think demand for booster shots could be lower than we had originally anticipated, based on the updated status of Moderna's advance purchase agreements for 2022 and management's discussion of a potential seasonal booster in the U.S. beginning in 2022. We have lowered our sales forecast for Moderna's COVID-19 vaccine to account for a potentially faster transition from a pandemic market to an endemic one, where doses may be reserved for higher-risk populations (including adults over age 65). However, this was countered by our decision to include probability-weighted sales for two rare disease programs in our model; mRNA-3927 (propionic acidemia) and mRNA-3705 (methylmalonic acidemia) have both entered phase 1. While this only adds $500 million in sales to our 2030 projections, the recurring nature of these potential sales is more meaningful to our DCF valuation than temporarily inflated COVID-19 sales. That said, we have only assigned these programs a 25% probability of approval, as proof-of-concept isn't expected until 2022 and intracellular protein targets are considered an unproven, higher-risk modality. Despite Moderna's massive success with its COVID-19 vaccine, we think the changing competitive landscape, virus evolution, and evolving safety and efficacy of its technology beyond COVID-19 create too many questions to grant the firm an economic moat, and we see shares as overvalued at recent prices.

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About the Author

Karen Andersen, CFA

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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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