Amid the COVID-19-fueled market correction, some stocks have performed well. In particular, several biotech companies that are racing to develop vaccines or treatments for the rapidly spreading disease have been crushing average market returns…
Shares of Inovio Pharmaceuticals (NASDAQ:INO) are up by 153% since the beginning of the year. In February, Inovio claimed it had developed a potential vaccine for COVID-19 in three hours after the genetic sequence for the SARS-CoV-2 virus that causes the disease was made public by Chinese researchers on Jan. 10.
The company is planning on starting clinical trials for its potential vaccine — dubbed INO-4800 — sometime this month. Similarly, shares of Moderna (NASDAQ:MRNA) — another biotech company racing to develop a vaccine for COVID-19 — are up by 66.5% year to date. Despite these stellar performances, though, both Inovio and Moderna seem like risky bets at this point. It is far from a sure bet that either one will successfully develop a vaccine for COVID-19, and neither has any approved product on the market yet. Investors looking for biotech stocks to buy should look elsewhere. One company whose stock I think is worth serious consideration is Acceleron Pharmaceuticals (NASDAQ:XLRN).
Could Reblozyl become a blockbuster drug?
Acceleron focuses on the development of treatments for rare diseases. The company currently has just one approved product, Reblozyl (luspatercept), a treatment for anemia in patients with beta-thalassemia who require regular blood transfusions. Beta-thalassemia is a rare blood disorder that leads to insufficient levels of beta-globin, an element of a protein in red blood cells called hemoglobin that carries oxygen in the body.
Patients with this condition also have insufficient red blood cells — a condition that is called anemia — which can lead to symptoms such as tiredness, or, much worse, the formation of blood clots. The U.S. Food and Drug Administration (FDA) approved Reblozyl in November of 2019. Acceleron estimates that there are about 1,000 to 1,500 beta-thalassemia patients in the U.S. who require regular blood transfusions. And while this market isn’t large, the company is looking to expand Reblozyl’s addressable market.
While the FDA’s recent approval of Reblozyl was for just one indication, Acceleron actually submitted Reblozyl to the FDA for review in April 2019 for two indications. The company is currently awaiting an FDA decision on Reblozyl as a treatment for anemia associated with myelodysplastic syndromes (MDS), a form of blood cancer.
Second, Acceleron also submitted a marketing authorization application (MAA) to the European Medicine Association (EMA) for Reblozyl in April 2019, and the company should receive the green light from the EMA in the second half of 2020. Acceleron estimates that the market for anemia-associated MDS in the U.S. is comprised of about 20,000 patients. This indication, and the potential approval of Reblozyl in Europe, should significantly expand the drug’s target market.
Another exciting product
Back in January, Acceleron’s shares soared by more than 50% after the company announced positive results from a phase 2 clinical trial studying the efficacy of sotatercept, an investigational treatment for pulmonary arterial hypertension (PAH), a condition marked by high blood pressure in the lungs. During the trial, patients treated with sotatercept demonstrated a statistically significant reduction in pulmonary vascular resistance — a measure of PAH severity — compared with patients treated with a placebo. Of course, that was only a phase 2 clinical trial, but…
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