On April 27, biotechnology company Moderna (MRNA -0.74%) announced its submission of an investigational new drug (IND) application to the U.S. Food and Drug Administration (FDA) to start phase 2 clinical trials related to its mRNA-1273 vaccine, which is being developed to fight the novel coronavirus.

Moderna's chief medical officer, Tal Zaks, said that the FDA had given the investigational vaccine a "fast track" designation to expedite clinical trials.

What is mRNA, and how can Moderna build a vaccine with it?

mRNA-1273 is developed on an mRNA vaccine platform. RNA -- ribonucleic acid -- is a molecule that's essential in the biological coding, decoding, regulation, and expression of genes.

IMAGE SOURCE: GETTY IMAGES.

IMAGE SOURCE: GETTY IMAGES.

mRNA, or "messenger RNA," serves as a sort of translator between genetic information in DNA and the amino acids and proteins that are necessary for life. One strand of mRNA corresponds to the genetic sequence of one strand of DNA; it's made in the nucleus of a cell and then travels to the cytoplasm, where cellular proteins are made. There, a minute particle called a ribosome moves along the mRNA, reads its base sequence, and uses the genetic code to translate it into a corresponding amino acid. 

A 2012 study published in the RNA Biology scientific journal posits that mRNA could theoretically be administered to prompt the development of vaccine proteins at the cellular level. That's been Moderna's focus since its founding in 2010, and the company creates its own synthetic mRNA for that purpose. While none of Moderna's products have yet reached final clinical trials, mRNA-1273 could change that.

Lonza and Moderna: a love story

On May 6, the FDA completed its review of Moderna's IND application, with the expectation that phrase 2 trials will begin in the coming weeks.

The Biomedical Advanced Research and Development Authority also awarded $483 million  to Moderna in April to support late-stage development programs expanding the scale of the company's manufacturing of mRNA-1273. That manufacturing includes a partnership with Swiss chemicals company Lonza Group A.G. (LZAGY -0.76%), which was launched May 1. The 10-year strategic collaboration and manufacturing agreement will enable the scaled-up manufacturing of mRNA-1273. 

All of this is a strong sign of significant long-term growth and (most importantly) a positive return on investment. Though the stock is already up 150% in the past year, Moderna remains a buy.

Novavax's obvious potential

It's also important to take note of vaccine developer Novavax (NVAX -2.24%), the NVX-COV2373 coronavirus vaccine it's working on, and that company's recent first-quarter financial results . Novavax is poised to be a game-changing investment that speaks to the post-pandemic potential of biotech and the value of investing in vaccines.

Like Moderna, Novavax is a solid buy. It's received a total of $388 million in research funding from the nonprofit Coalition for Epidemic Preparedness Innovations (CEPI), which will fund preclinical studies and phase 1 and 2 clinical trials of the vaccine. CEPI anticipates supporting the clinical development of NVX-CoV2373 through licensure with manufacturers.

Financial results and a flu vaccine could seal the deal

The company's first-quarter results outperformed expectations, with a quarterly loss of $0.58 per share looking much better than last year's $2.20 loss.

Novavax could be a long-term potential — similar to Moderna's — in a post-pandemic world. While management said  much of the better-than-expected first-quarter earnings were tied to the potential of NVX-CoV2373, the company's NanoFlu program also looks promising as a potential  boost to long-term earnings. NanoFlu is Novavax's answer to other existing influenza vaccines, and it is expected to challenge Sanofi S.A.'s (SNY 0.62%) Fluzone  vaccine.

Phase 3 trials for NanoFlu outperformed Fluzone on the measures of immunogenicity. The Novavax entry is a nanoparticle flu vaccine that makes it an insect cell system. This trial enrolled a randomized cohort of 2,652 adults aged 65 years classified as health . These people received either NanoFlu or Fluzone Quadrivalent. After the extent of the trial, NanoFlu matched or beats Fluzone in most metrics. National Library of Medicine clinical trial disclosures can provide more context to the comparison.