CRISPR Therapeutics Stock (NASDAQ:CRSP) Pushes Lower, But Fundamentals Are Intact

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CRISPR Therapeutics (NASDAQ:CRSP) stock has been slowly heading lower in recent months, and I don’t think that’s fair. Having reached highs near $90 a share, the stock is now trading at closer to $55. But rather than any bad news, the falling share price reflects the absence of any big updates after the company achieved regulatory approval for its novel gene-editing treatment in the UK and U.S. in November and December.

Given the potential market value of its greenlit treatment and the potential of the company’s pipeline, I think CRISPR is significantly undervalued. I’m bullish on CRSP stock.

CRSP stock has been falling in recent months.
CRSP stock has been falling in recent months.

What Is CRISPR Therapeutics?

CRISPR Therapeutics is a Swiss company at the forefront of gene editing. The company harnesses CRISPR-Cas9, a tool inspired by bacteria’s defense system and co-invented by Dr. Emmanuelle Charpentier, one of the CRISPR Therapeutics founders. The technology can be understood by looking at its three constituent parts:

  • CRISPR: this stands for “Clustered Regularly Interspaced Short Palindromic Repeats” of genetic information that some bacteria use as part of an antiviral system,

  • Cas9: a CRISPR-associated (Cas) endonuclease, or enzyme, that acts as “molecular scissors” to cut DNA,

  • Guide RNA (gRNA): a type of ribonucleic acid (RNA) molecule that binds to Cas9 and guides it to where the DNA needs to be cut.

This technology provides a potential cure for a range of illnesses that we haven’t been able to treat, such as sickle-cell disease (SCD) and certain cancers. CRISPR Therapeutics has built a diverse portfolio of treatments across a broad range of disease areas, including hemoglobinopathies (like SCD), oncology, diabetes, and cardiovascular disease.

Its partnership with Vertex Pharmaceuticals (NASDAQ:VRTX) has led to the development of CASGEVY, the first CRISPR-based therapy for specific blood disorders. Not only was this the first CRISPR approval for specific blood disorders, but it was the first gene-editing approval globally. CRISPR Therapeutics is very much at the forefront of this technology, bringing the promise of gene-editing therapies across multiple areas of research closer to reality.

Is CRISPR Therapeutics Commercially Viable?

To date, the Swiss firm has only earned money through achieving milestone payments from Vertex. However, with CASGEVY receiving regulatory approval for the treatment of SCD and transfusion‑dependent beta-thalassemia in the UK, U.S., EU, and Saudi Arabia, among other places, CRISPR Therapeutics is moving towards generating revenue from commercial activities.