Investing $1,000 in These 3 Beaten-Down Stocks Could Be a Brilliant Move

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Investing in stocks that aren't performing well can be a good move, but only if there are good reasons to think they will recover. That isn't the case for many companies that have lagged broader equities.

While it can be hard to separate the wheat from the chaff, let's consider three companies, all in the biotech industry, that were market losers last year but could recover given enough time: CRISPR Therapeutics (NASDAQ: CRSP), Amgen (NASDAQ: AMGN), and Regeneron (NASDAQ: REGN).

If you have $1,000 to spare (don't dip into money earmarked for important things or a rainy day!), here's why it might be worth investing in these drugmakers.

1. CRISPR Therapeutics

CRISPR Therapeutics is the gene-editing specialist that created Casgevy, a treatment for sickle cell disease (SCD) and transfusion-dependent beta-thalassemia (TDT), which it developed with Vertex Pharmaceuticals. Though it has now been a commercial-stage company for more than a year, CRISPR isn't generating much revenue yet from its first approved product, since gene-editing therapies take time to administer.

The minimal revenue, combined with the fact that CRISPR Therapeutics is still unprofitable, makes the stock a bit risky. That's why investors are skeptical of the biotech's prospects. However, Casgevy's potential is enormous. There are few competing therapies for SCD or TDT, especially in the Middle East, a market that CRISPR Therapeutics and Vertex are targeting. The two partners estimate a patient population of at least 58,000 people in the region.

It might take some time, but Casgevy should make headway and help improve CRISPR Therapeutics' financial results. Furthermore, the mid-cap drugmaker has several other exciting candidates.

Last year, the U.S. Food and Drug Administration (FDA) granted the regenerative medicine advanced therapy (RMAT) designation to CRISPR's CTX112, an investigational treatment for certain B-cell malignancies. This designation is reserved for therapies that meet specific criteria, including targeting areas with high unmet needs and producing encouraging early data in clinical trials. It's no guarantee of approval, but it's a good start.

More importantly, CRISPR Therapeutics' gene-editing platform has the potential to unlock more medicines for other difficult-to-treat conditions, as it's already proven with Casgevy. The company might be down right now, but solid clinical and regulatory progress in the next few years, coupled with increasing revenue from Casgevy, could allow it to bounce back.