Updated Aug 12 at 4:02pm ET.
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The U.S. Food and Drug Administration approved Moderna's seasonal flu vaccine, mFLUSIVA, for adults aged 50 and older. This is the first time a flu shot using messenger RNA (mRNA) technology, the same method used for COVID-19 vaccines, has been cleared for use. The company expects to have the vaccine available at some retailers in the coming weeks.
This approval is a critical milestone for the company's plan to move beyond its dependence on COVID-19 sales. By entering the flu market, Moderna is trying to prove its technology can compete in a crowded field of traditional vaccines. Success here is vital for the company to reach its goal of growing revenue as pandemic-related demand continues to fade.
Source: Barrons
Moderna has begun its first human trial for an experimental vaccine designed to protect against the Bundibugyo strain of Ebola. This specific strain has caused deadly outbreaks in the past and currently has no approved vaccine. The study is being conducted in Canada and will test if the shot is safe and triggers an immune response.
While this is an early-stage trial and far from a finished product, it shows the company is using its mRNA platform to tackle diseases that traditional vaccine makers have struggled to address. For long-term owners, this is another example of how the company aims to build a broad portfolio of specialized vaccines beyond its well-known respiratory business.
Source: Barrons
Moderna reported a loss of $1.97 per share for the second quarter, which was slightly better than the $2.03 loss analysts expected. Revenue reached $140 million, also beating expectations. The company improved its full-year outlook by cutting about $200 million in expected operating expenses and raising its year-end cash target to between $4.7 billion and $5.2 billion.
However, the results were mixed. While the company is doing a better job of controlling its spending, it faced a setback with its norovirus vaccine candidate, which failed to meet the criteria for early success in a Phase 3 trial. The stock fell as the market remains focused on the ongoing decline in COVID-19 vaccine sales and the pressure on management to prove the next wave of products can fill that gap.
See the full quarter, and how our tracked metrics did
Source: 8-K filing
Goldman Sachs raised its price target for Moderna to $67, up from a previous target of $49. This new target is about 23 percent higher than the current stock price. Despite the higher target, the firm kept its rating at neutral, which suggests they see the stock as fairly valued rather than a clear buy right now.
The move indicates that some analysts are becoming more optimistic about the value of the company's pipeline as it moves toward several key data readouts. While the stock has been volatile, this target increase reflects a belief that the company's long-term potential is higher than previously estimated.
Source: Goldman Sachs
Wolfe Research set a new price target for Moderna at $25. This is significantly lower than the current trading price of about $54 and well below the average analyst target of $46.
A target this low suggests a very skeptical view of the company's ability to replace its lost COVID-19 revenue with new products. It highlights the risk that if upcoming clinical trials or product launches fail to meet high expectations, the stock could have much further to fall.
Source: Wolfe Research
Analysts have recently adjusted their price targets following the company's steady stream of updates and vaccine approvals. Most experts are cautious, with 20 of 27 rating the stock as neutral or bearish, and the average target sits 28% below today's price.
The company has beaten analyst profit targets for eight straight quarters. This suggests management is doing a good job of controlling costs even as their main source of revenue shrinks.
| Expectation | |
|---|---|
| EPS | $-1.38 |
| Revenue | $873M |